Class   564	ORGANIC COMPOUNDS -- PART OF THE CLASS 532-570 SERIES
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This Class 564 is considered to be an integral part of Class 260 (see the Class 260 schedule for the position of this Class in schedule hierarchy). This Class retains all pertinent definitions and class lines of Class 260.

ORGANIC COMPOUNDS (CLASS 532, SUBCLASS 1)

1

. (1 indent ) AMINO NITROGEN CONTAINING (E.G., UREA, SULFONAMIDES, NITROSAMINES, OXYAMINES, ETC., AND SALTS THEREOF)

1.5

.. (2 indent ) Adducts or inclusion compounds of urea per se or of of thiourea per se with organic compounds (e.g., urea-alkane inclusion compounds, etc.)

2

.. (2 indent ) With preservative or stabilizer

3

... (3 indent ) Ureas or thioureas with preservative or stabilizer

4

... (3 indent ) Carboxamides with preservative or stabilizer

5

... (3 indent ) Benzene ring containing compound with preservative or stabilizer

6

.... (4 indent ) Inorganic preservative or stabilizer

7

.... (4 indent ) Sulfur or phenol containing preservative or stabilizer

8

.. (2 indent ) Boron containing (e.g., boron containing complexes, salts, etc.)

9

... (3 indent ) Boron attached directly to amino nitrogen by nonionic bonding

10

.... (4 indent ) The boron and amino nitrogen are members of the same ring

11

....• (5 indent ) Polycyclo ring system having the nitrogen and boron containing ring as one of the cyclos

12

.. (2 indent ) Phosphorus attached directly to amino nitrogen by nonionic bonding

13

... (3 indent ) The phosphorus and nitrogen are members of the same ring

14

... (3 indent ) Chalcogen and plural nitrogens bonded directly to the same phosphorus

15

.. (2 indent ) Phosphorus attached indirectly to amino nitrogen by nonionic bonding

16

... (3 indent ) The phosphorus is a ring member

17

.. (2 indent ) Thioureas (i.e., HNH-C(=S)-HNH, wherein substitution may be made for hydrogen only)

18

... (3 indent ) Thiocarbazides or thiosemicarbazides (i.e. HNH-NH-C(=S)-HNH, wherein the N bonded directly to the thiourea N is an amino N and substitution may be made for hydrogen only)

19

.... (4 indent ) Thiocarbazones or thiosemicarbazones (i.e., HCH=N-NH-C(=S)-HNH, wherein substitution may be made for hydrogen only)

20

....• (5 indent ) Benzene ring containing

21

....•. (6 indent ) Additional nitrogen attached indirectly to the thiocarbonyl by nonionic bonding

22

... (3 indent ) Thiobiurets (i.e., HNH-C(=S)-NH-C(=X)-HNH, wherein X is S or O and substitution may be made for hydrogen only)

23

... (3 indent ) Carbonyl, sulfur, or cyano attached directly to thiourea nitrogen by nonionic bonding

24

... (3 indent ) Processes utilizing carbon disulfide

25

... (3 indent ) Processes utilizing cyano containing compound

26

... (3 indent ) Benzene ring containing

27

.... (4 indent ) Nitrogen attached indirectly to the thiocarbonyl by nonionic bonding

28

.... (4 indent ) Hydroxy, bonded directly to carbon, or ether containing (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

29

.... (4 indent ) Halogen attached indirectly to the thiocarbonyl by nonionic bonding

30

... (3 indent ) Acyclic

31

.... (4 indent ) Thiourea per se or salt thereof

32

.. (2 indent ) Ureas (i.e., HNH-CO-HNH, wherein substitution may be made for hydrogen only)

33

... (3 indent ) Nitro or nitroso bonded directly to nitrogen

34

... (3 indent ) Carbazides or semicarbazides (i.e., HNH-NH-CO-HNH, wherein substitution may be made for hydrogen only)

35

.... (4 indent ) Carbonyl or sulfur attached directly to carbazide or semicarbazide nitrogen by nonionic bonding

36

.... (4 indent ) Carbazones or semicarbazones (i.e., HCH=N-NH-CO-HNH, wherein substitution may be made for hydrogen only)

37

.... (4 indent ) Acyclic

38

... (3 indent ) Biurets (i.e., HNH-CO-NH-CO-HNH, wherein substitution may be made for hydrogen only)

39

... (3 indent ) Sulfur attached directly to urea nitrogen by nonionic bonding

40

.... (4 indent ) The sulfur is part of a substituent which contains nitrogen

41

....• (5 indent ) The substituent nitrogen is the nitrogen of a benzamido group (e.g., Cl benzene-CO-NH-HCH-(O=)S(=O)-, bonded directly to urea nitrogen, etc.)

42

.... (4 indent ) The sulfur is part of a monocyclic benzene ring containing substituent

43

....• (5 indent ) Alicyclic ring bonded directly to urea nitrogen

44

... (3 indent ) Additional carbonyl bonded directly to urea nitrogen

45

.... (4 indent ) The additional carbonyl is in a substituent which is acyclic

46

....• (5 indent ) Carbon to carbon unsaturation in the substituent

47

... (3 indent ) Benzene ring containing

48

.... (4 indent ) Benzene ring bonded directly to urea nitrogen (i.e., anilides)

49

....• (5 indent ) The benzene ring is part of a substituent which contains sulfur

50

....• (5 indent ) The benzene ring is part of a substituent which contains nitrogen

51

....•. (6 indent ) The substituent nitrogen is attached indirectly to the benzene ring by acyclic nonionic bonding

52

....• (5 indent ) The benzene ring is part of a substituent which contains oxygen

53

....• (5 indent ) The benzene ring is part of a substituent which contains halogen bonded directly to carbon

54

....•. (6 indent ) The halogen is fluorine

55

....• (5 indent ) Plural benzene rings bonded directly to urea nitrogen

56

.... (4 indent ) Aralkyl bonded directly to urea nitrogen

57

... (3 indent ) Alicyclic ring containing

58

... (3 indent ) Additional carbon bonded directly to urea nitrogen

59

.... (4 indent ) The additional carbon is part of a substituent which contains nitrogen

60

.... (4 indent ) The additional carbon is part of a substituent which contains oxygen

61

.... (4 indent ) Processes

62

....• (5 indent ) Preparing directly from compound having carbon to carbon unsaturation

63

... (3 indent ) Urea per se or salt thereof

64

.... (4 indent ) Preparing directly from cyano containing compound

65

.... (4 indent ) Preparing directly from ammonia and carbonmonoxide or carbon oxysulfide (e.g., from ammonia and COS, etc.)

66

.... (4 indent ) Preparing directly from ammonium carbamate (i.e., from HNH-COO-HHNHH)

67

.... (4 indent ) Preparing directly from ammonia and carbon dioxide

68

....• (5 indent ) With corrosion inhibiting of reactor

69

....• (5 indent ) With ammonia synthesis

70

....• (5 indent ) With decomposition of by-product ammonium carbamate (i.e., decomposition of HNH-COO-HHNHH)

71

....•. (6 indent ) Utilizing indirect heat exchange

72

....•. (6 indent ) In plural stages

73

.... (4 indent ) Purification or recovery

74

.. (2 indent ) Thiocarboxamides (i.e., compounds containing -C(=S)-HNH, wherein substitution may be made for hydrogen only)

75

... (3 indent ) Sulfur bonded directly to the thiocarbonyl

76

.... (4 indent ) Thiuram sulfides (e.g., HNH-C(=S)-S-S-C(=S)-HN-alkyl, etc.)

77

... (3 indent ) Thiooxamides (i.e., HNH-C(=S)-C(=X)-HNH, wherein X is S or O and substitution may be made for hydrogen only)

78

... (3 indent ) Acyclic

79

.. (2 indent ) Sulfamides (i.e., HNH-(O=)S(=O)-HNH, wherein substitution may be made for hydrogen only)

80

.. (2 indent ) Sulfonamides (i.e., Q-(O=)S(=O)-HNH, wherein Q is a substituent and wherein any substituent replacing one or both hydrogens shown will be referred to as E)

81

... (3 indent ) Hydrazine containing

82

... (3 indent ) Plural sulfonamide groups containing or containing plural sulfonyls bonded directly to the same nitrogen

83

.... (4 indent ) Two sulfonamido sulfonyls having no sulfonamido nitrogen between the sulfonyls

84

... (3 indent ) Substituent Q contains benzene ring

85

.... (4 indent ) Sulfur in substituent Q

86

.... (4 indent ) Nitrogen in substituent Q

87

....• (5 indent ) Nitro or nitroso in substituent Q

88

.... (4 indent ) Carbonyl in substituent Q

89

.... (4 indent ) Hydroxy, bonded directly to carbon, or ether in substituent Q (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

90

.... (4 indent ) Substituent Q is monocyclic

91

....• (5 indent ) Carbonyl, cyano, nitro, nitroso, halogen, or sulfur attached directly to the sulfonamide nitrogen or to an amino nitrogen in a substituent E by nonionic bonding

92

....• (5 indent ) Benzene ring in a substituent E

93

....• (5 indent ) Hydroxy, bonded directly to carbon, or ether in a substituent E (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

94

....• (5 indent ) Nitrogen in an acyclic substituent E

95

... (3 indent ) Substituent Q is acyclic

96

.... (4 indent ) Halogen in substituent Q attached indirectly to the sulfonamide sulfur by nonionic bonding

97

....• (5 indent ) Benzene ring in a substituent E

98

.... (4 indent ) Substituent Q is alkyl

99

....• (5 indent ) Benzene ring in a substituent E

100

.. (2 indent ) Sulfur and amino nitrogen attached directly to the same sulfur by nonionic bonding

101

.. (2 indent ) Plural amino nitrogens attached directly to the same sulfur, or oxygen double bonded and amino nitrogen attached directly to the same sulfur, all by nonionic bonding (e.g., sulfinamides, etc.)

102

.. (2 indent ) Sulfur attached directly to amino nitrogen by nonionic bonding (e.g., sulfenamides, etc.)

103

.. (2 indent ) Cyanamides (i.e., compounds containing cyano bonded directly to amino nitrogen)

104

... (3 indent ) Cyanoguanidines (i.e., HNH-C(=NH)-HNH, wherein -CN is substituted for one of the hydrogens and substitution may be made for the remaining hydrogens only)

105

... (3 indent ) Benzene ring containing

106

... (3 indent ) Acyclic

107

.. (2 indent ) Nitramines (i.e., compounds containing nitro bonded directly to amino nitrogen)

108

... (3 indent ) Containing nitrogen double bonded directly to carbon (e.g., nitroguanidines, etc.)

109

... (3 indent ) Acyclic

110

.... (4 indent ) Containing nitro bonded directly to carbon (i.e., plural nitro groups containing)

111

....• (5 indent ) Hydroxy, bonded directly to carbon, or ether containing (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

112

.. (2 indent ) Nitrosamines (i.e., compounds containing nitroso bonded directly to amino nitrogen)

113

... (3 indent ) Acyclic

114

.. (2 indent ) Haloamines (i.e., compounds containing halogen attached directly to amino nitrogen by nonionic bonding)

115

... (3 indent ) Containing nitrogen double bonded directly to carbon

116

.... (4 indent ) Amidine containing (i.e., containing -C(=N)-HNH, wherein substitution may be made for hydrogen only)

117

... (3 indent ) Alicyclic ring containing

118

... (3 indent ) Acyclic

119

.... (4 indent ) Hydroxy, bonded directly to carbon, or ether containing (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

120

.... (4 indent ) Carbon to carbon unsaturation containing

121

.... (4 indent ) Plural difluoramine groups containing

122

....• (5 indent ) Plural difluoramine groups bonded directly to the same carbon

123

.. (2 indent ) Carboxamides (i.e., Q-CO-HNH, wherein Q is a substituent having carbon bonded directly to the carbonyl or is hydrogen and wherein any substituent replacing one or both hydrogens shown will be referred to as E)

124

... (3 indent ) Preparing directly from cyano containing compound

125

.... (4 indent ) From HCN or cyanogen

126

.... (4 indent ) Catalytic hydration only of nitrile

127

....• (5 indent ) Copper containing catalyst utilized

128

....• (5 indent ) Of acrylonitriles

129

.... (4 indent ) Acid hydrolysis only of nitrile

130

.... (4 indent ) From acyclic nitrile

131

....• (5 indent ) Which contains carbon to carbon unsaturation

132

... (3 indent ) Preparing directly from carbon monoxide or carbon dioxide

133

... (3 indent ) Preparing directly by amidation of -C(=O)X group, where X is O- or halogen

134

.... (4 indent ) Of carboxylic acid ester

135

....• (5 indent ) Having acyclic acid moiety

136

....•. (6 indent ) Additional oxygen in the acid moiety

137

....•. (6 indent ) Lower fatty acid

138

.... (4 indent ) Of carboxylic acid

139

....• (5 indent ) Benzene ring containing

140

....•. (6 indent ) Hydroxy naphthoic

141

....• (5 indent ) Lower fatty acid

142

.... (4 indent ) Of carboxylic acid halide

143

....• (5 indent ) Acyclic

144

.... (4 indent ) Of acyclic carboxylic acid anhydride

145

... (3 indent ) Preparing directly by reacting sulfur or sulfur containing compound with ammonia; or directly from ammonium polysulfide

146

... (3 indent ) Preparing directly by nitration

147

... (3 indent ) Aminimine containing

148

... (3 indent ) Hydrazine containing

149

.... (4 indent ) Substituent Q contains benzene ring

150

....• (5 indent ) Hydroxy, bonded directly to carbon, or ether in substituent Q (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

151

.... (4 indent ) Substituent Q is acyclic

152

... (3 indent ) Plural carboxamide groups containing or containing plural carbonyls bonded directly to the same nitrogen

153

.... (4 indent ) Three or more carboxamide groups

154

.... (4 indent ) Sulfur containing

155

.... (4 indent ) Benzene ring containing

156

....• (5 indent ) Two carboxamido carbonyls having benzene ring between the carbonyls and no carboxamido nitrogen between the carbonyls

157

....• (5 indent ) Amino nitrogen, not bonded directly to carbonyl, containing

158

....• (5 indent ) Hydroxy, bonded directly to carbon, or ether containing (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

159

.... (4 indent ) Acyclic

160

....• (5 indent ) Two carboxamido carbonyls having no carboxamido nitrogen between the carbonyls

161

... (3 indent ) Substituent Q contains benzene ring

162

.... (4 indent ) Sulfur in substituent Q

163

.... (4 indent ) Nitrogen in substituent Q

164

....• (5 indent ) The substituent nitrogen is an amino nitrogen attached indirectly to a ring by acyclic nonionic bonding

165

....•. (6 indent ) Hydroxy, bonded directly to carbon, or ether in substituent Q (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

166

....• (5 indent ) Nitro in substituent Q

167

....• (5 indent ) Hydroxy, bonded directly to carbon, or ether in substituent Q (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

168

....• (5 indent ) Ring in a substituent E

169

.... (4 indent ) Carbonyl in substituent Q

170

.... (4 indent ) Hydroxy, bonded directly to carbon, or ether in substituent Q (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

171

....• (5 indent ) Plural rings in substituent Q

172

....•. (6 indent ) Polycyclo ring system in substituent Q

173

....•.. (7 indent ) Q contains an ortho-hydroxy naphthyl bicyclo ring system, or its partially hydrogenated form, bonded directly to the carbonyl (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

174

....•. (6 indent ) Ring in a substituent E

175

....• (5 indent ) Oxygen, bonded directly to the benzene ring, is part of an acyclic chain between the benzene ring and the carbonyl

176

....• (5 indent ) Benzene ring bonded directly to the carbonyl

177

....•. (6 indent ) Hydroxy bonded directly to the benzene ring (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

178

....•.. (7 indent ) Preparing directly by halogenation

179

....•.. (7 indent ) Benzene ring in a substituent E

180

.... (4 indent ) Polycyclo ring system in substituent Q

181

.... (4 indent ) Two rings bonded directly to the same carbon in substituent Q

182

.... (4 indent ) Substituent Q is monocyclic

183

....• (5 indent ) The ring is bonded directly to the carbonyl

184

....•. (6 indent ) Benzene ring in a substituent E

185

....•.. (7 indent ) Ring or polycyclo ring system in substituent E is attached indirectly to the carboxamide nitrogen or to an amino nitrogen in substituent E by acyclic nonionic bonding

186

....•. (6 indent ) Oxygen in a substituent E

187

....•. (6 indent ) Acyclic carbon to carbon unsaturation in a substituent E

188

... (3 indent ) Plural alicyclic rings in substituent Q

189

... (3 indent ) Five-membered ring in substituent Q

190

... (3 indent ) Three-membered ring in substituent Q

191

... (3 indent ) Alicyclic ring and an atom other than oxygen, carbon, or hydrogen in substituent Q

192

... (3 indent ) Substituent Q is acyclic

193

.... (4 indent ) Nitrogen in substituent Q

194

....• (5 indent ) Benzene ring in a substituent E

195

....•. (6 indent ) Two rings bonded directly to the same carbon in a substituent E

196

....•. (6 indent ) A ring or polycyclo ring system in a substituent E is attached indirectly to the carboxamide nitrogen or to an amino nitrogen in substituent E by acyclic nonionic bonding

197

....• (5 indent ) The compound is acyclic

198

....•. (6 indent ) The carboxamide nitrogen is unsubstituted

199

.... (4 indent ) Carbonyl in substituent Q

200

....• (5 indent ) Benzene ring in a substituent E

201

.... (4 indent ) Hydroxy, bonded directly to carbon, or ether in substituent Q (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

202

....• (5 indent ) Benzene ring in a substituent E

203

....• (5 indent ) Hydroxy, bonded directly to carbon, or ether in an acyclic substituent E (Hof -OH may be replaced by a substituted or unsubstututed ammonium ion or a Group IA or IIA light metal)

204

.... (4 indent ) Carbon to carbon unsaturation in substituent Q

205

....• (5 indent ) Process which includes forming the unsaturation

206

....• (5 indent ) Purification or recovery

207

....• (5 indent ) Benzene ring in a substituent E

208

....• (5 indent ) Hydroxy, bonded directly to carbon, or ether in an acyclic substituent E (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

209

.... (4 indent ) Halogen, bonded directly to carbon, in substituent Q

210

....• (5 indent ) Ring in a substituent E

211

....•. (6 indent ) Benzene ring in a substituent E

212

....•.. (7 indent ) A ring or polycyclo ring system in a substituent E is attached indirectly to the carboxamide nitrogen or to an amino nitrogen in substituent E by acyclic nonionic bonding

213

....•... (8 indent ) Nitro and hydroxy, bonded directly to carbon, or ether in the substituent E (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

214

....•.. (7 indent ) The compound is monocyclic

215

.... (4 indent ) Q is hydrogen or a lower saturated alkyl substituent

216

....• (5 indent ) Purification or recovery

217

....• (5 indent ) Ring in a substituent E

218

....•. (6 indent ) Benzene ring in a substituent E

219

....•.. (7 indent ) A ring or polycyclo ring system in a substituent E is attached indirectly to the carboxamide nitrogen or to an amino nitrogen in substituent E by acyclic nonionic bonding

220

....•... (8 indent ) Amino nitrogen in the substituent E (i.e.,plural amino nitrogens containing)

221

....•.. (7 indent ) Plural rings in a substituent E

222

....•... (8 indent ) Polycyclo ring system in a substituent E

223

....•.. (7 indent ) Hydroxy, bonded directly to carbon, or ether in a substituent E (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

224

....• (5 indent ) Hydroxy, bonded directly to carbon, ether or nitrogen in a substituent E (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

225

.. (2 indent ) Amidines (i.e., HN=CH-HNH, wherein substition may be made for hydrogen only)

226

... (3 indent ) Amidino hydrazines or hydrazones (i.e., HNH-N=CH-HNH or HN=CH-NH-HNH, wherein substitution may be made for hydrogen only)

227

.... (4 indent ) Guanyl hydrazines or hydrozones (i.e., HNH-N=C(-HNH)-HNH or HN=C(-HNH)-NH HNH, wherein substitution may be made for hydrogen only)

228

....• (5 indent ) Benzene ring containing

229

... (3 indent ) Amidoximes (i.e., HON=CH-HNH, wherein substitution may be made for hydrogen only)

230

... (3 indent ) Guanidines (i.e., HN=C(-HNH)-HNH, wherein substitution may be made for hydrogen only)

231

.... (4 indent ) Preparing from thioureas

232

.... (4 indent ) Preparing by reacting cyanogen halide with amino nitrogen containing compound

233

.... (4 indent ) Biguanides (i.e., HN=C(-HNH)-NH-(HNH-)C=NH, wherein substitution may be made for hydrogen only)

234

....• (5 indent ) Benzene ring containing

235

....•. (6 indent ) Plural rings containing

236

.... (4 indent ) Polyguanidines

237

.... (4 indent ) Benzene ring containing

238

....• (5 indent ) Benzene ring bonded directly to guanidine nitrogen

239

....•. (6 indent ) Hydroxy, bonded directly to carbon, or ether containing (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

240

.... (4 indent ) Acyclic

241

....• (5 indent ) Guanidine per se or salt thereof

242

....•. (6 indent ) Guanidine nitrate

243

... (3 indent ) Polyamidines

244

... (3 indent ) Benzene ring containing

245

.... (4 indent ) N(prime)-aryl formimidines (i.e., benzene-N=CH-HNH, wherein substitution may be made for hydrogen, including those bonded directly to the benzene ring only)

246

.... (4 indent ) Additional nitrogen attached indirectly to amidine nitrogen by nonionic bonding

247

.... (4 indent ) Hydroxy, bonded directly to carbon, or ether containing (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

248

.. (2 indent ) Containing nitrogen double bonded directly to carbon

249

... (3 indent ) Azines (i.e., HCH=N-N=HCH, wherein substitution may be made for hydrogen)

250

... (3 indent ) Hydrazones (i.e., HCH=N-HNH, wherein substitution may be made for hydrogen only)

251

.... (4 indent ) Benzene ring containing

252

... (3 indent ) Carbodiimides (i.e., HN=C=NH, wherein substitution may be made for hydrogen only)

253

... (3 indent ) Oximes (HCH=N-OH, i.e., wherein substitution may be made for hydrogen only)

254

.... (4 indent ) O-esters (i.e., H of oxime -OH replaced by ester forming group)

255

....• (5 indent ) O-carbamoyl

256

.... (4 indent ) O-ethers (i.e., H of oxime -OH replaced by ether forming group)

257

....• (5 indent ) Polycyclo ring system

258

.... (4 indent ) Oxygen double bonded, or hydroxy or ether oxygen bonded directly to an alpha carbon (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group Ia or IIA light metal)

259

.... (4 indent ) Preparing directly by reacting carbonyl with hydroxylamine or salt thereof

260

.... (4 indent ) Preparing directly by reducing nitronic acid salt

261

.... (4 indent ) Preparing directly by reducing nitro group

262

.... (4 indent ) Preparing directly by oxidizing a hydroxyl amine

263

.... (4 indent ) Preparing directly by nitrosation of olefin

264

.... (4 indent ) Purification or recovery

265

.... (4 indent ) Benzene ring containing

266

....• (5 indent ) The oxime carbon is acyclic and has two rings bonded directly thereto

267

.... (4 indent ) Six-membered alicyclic ring double bonded directly to the oxime nitrogen

268

.... (4 indent ) Acyclic

269

... (3 indent ) Nitrogen double bonded and two rings bonded directly to the same acyclic carbon (e.g., auramines, etc.)

270

... (3 indent ) Polycyclo ring system

271

... (3 indent ) Aldimines or ketimines which contain benzene ring (i.e., HCH=NH, wherein substitution may be made for hydrogen only but a hydrogen or carbon must be bonded directly to the carbon)

272

.... (4 indent ) Benzylidene imines (i.e., Q-benzene-CH=NH, wherein Q is a substituent or hydrogen and substitution may be made for hydrogen only)

273

....• (5 indent ) Substituent Q contains nitrogen bonded directly to carbon

274

....• (5 indent ) Substituent Q contains hydroxy, bonded directly to carbon, or ether (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

275

....• (5 indent ) Q is hydrogen only

276

.... (4 indent ) Hydroxy, bonded diretly to carbon, or ether containing (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

277

.... (4 indent ) Unsubstituted phenyl bonded directly to the aldimine or ketimine nitrogen

278

... (3 indent ) Aldimines or ketimines which are acyclic

279

.... (4 indent ) Carbon to carbon unsaturation containing

280

.. (2 indent ) Phenol or thiophenol addition salts

281

.. (2 indent ) Quaternary ammonium containing

282

... (3 indent ) Benzene ring containing

283

.... (4 indent ) Two rings bonded directly to the same carbon

284

.... (4 indent ) Nitro or nitroso, bonded directly to carbon containing

285

.... (4 indent ) Hydroxy, bonded directly to carbon, or ether containing (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

286

....• (5 indent ) Polyquaternary ammonium

287

....• (5 indent ) The hydroxy or ether oxygen is bonded directly to a ring

288

.... (4 indent ) Acyclic carbon to carbon unsaturation containing

289

.... (4 indent ) Halogen attached indirectly to the ammonium nitrogen by nonionic bonding

290

.... (4 indent ) Polyquaternary ammonium

291

... (3 indent ) Acyclic

292

.... (4 indent ) Hydroxy, bonded directly to carbon, or ether containing (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

293

....• (5 indent ) Choline, beta-alkylcholines, ethers thereof, and salts thereof

294

....• (5 indent ) Polyoxyalkylene

295

.... (4 indent ) Polyquaternary ammonium

296

.... (4 indent ) Processes

297

.. (2 indent ) Amine oxides

298

... (3 indent ) Processes

299

... (3 indent ) Benzene ring containing

300

.. (2 indent ) Nitroxides, oxyamines or hydroxylamines (i.e., HNH-O or HNH-OH, wherein substitution may be made for hydrogen only, including O-ether and O-ester derivatives)

301

... (3 indent ) Acyclic

302

.. (2 indent ) Racemization per se or with resolution of optical isomers

303

.. (2 indent ) Resolution per se of optical isomers

304

... (3 indent ) Of benzene ring containing compounds

305

.. (2 indent ) Benzene ring containing

306

... (3 indent ) Alicyclic ring or ring system, having plural amino nitrogens attached directly or indirectly thereto by acyclic nonionic bonding, attached indirectly to an aryl ring or ring system by acyclic nonionic bonding

307

... (3 indent ) Amino nitrogen and a ring bonded directly to the same ring, and any other amino nitrogen in the compound is bonded directly to one of the rings

308

.... (4 indent ) Polycyclo ring system

309

.... (4 indent ) Benzidines

310

... (3 indent ) Hydrazines

311

.... (4 indent ) Symmetrical diaryl hydrazines

312

....• (5 indent ) Preparing directly by reducing nitrogen containing group with metal and metallic hydroxide

313

.... (4 indent ) Aralkyl hydrazines

314

.... (4 indent ) Processes

315

... (3 indent ) Two aryl rings or ring systems bonded directly to the same carbon

316

.... (4 indent ) Amino nitrogen attached to the carbon by an acyclic carbon or chain

317

....• (5 indent ) Oxygen or sulfur is bonded directly to the carbon and is part of the chain

318

....•. (6 indent ) Processes

319

....• (5 indent ) Oxygen, carbonyl or carbon to carbon unsaturation in the chain; or ether, carbonyl, carbon to carbon unsaturation or hydroxy, bonded directly to carbon, is part of a substituent bonded directly to the acyclic carbon or chain (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

320

....• (5 indent ) Hydroxy or ether oxygen bonded directly to the carbon (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

321

.... (4 indent ) Amino nitrogen bonded directly to the carbon

322

.... (4 indent ) The carbon is a ring member of an alicyclic ring or ring system

323

.... (4 indent ) Amino nitrogen attached to aryl ring or ring system by an acyclic carbon or chain

324

....• (5 indent ) Oxygen or sulfur is bonded directly to the aryl ring or ring system and is part of the chain

325

....•. (6 indent ) Additional similar chain

326

....• (5 indent ) Amino nitrogen is bonded directly to the aryl ring or ring system and is part of the chain

327

.... (4 indent ) Benzhydrols or benzthiols (i.e., -OH or -SH bonded directly to the carbon)

328

.... (4 indent ) Benzophenones or benzothiophenones (i.e., the carbon is part of a carbonyl or thiocarbonyl)

329

....• (5 indent ) Processes

330

.... (4 indent ) Diamino diphenyl methanes (i.e., two phenyls, each having amino nitrogen bonded directly thereto, bonded directly to the carbon)

331

....• (5 indent ) Preparing by reacting carbonyl containing compound with amino nitrogen containing compound

332

....•. (6 indent ) Solid catalyst utilized

333

....•. (6 indent ) Hydrochloric acid utilized

334

....• (5 indent ) Purification or recovery

335

....• (5 indent ) Halogen or sulfur attached directly or indirectly to the carbon by nonionic bonding

336

... (3 indent ) Amino nitrogen attached to aryl ring or ring system by an acyclic carbon or chain

337

.... (4 indent ) The aryl ring or ring system is bonded directly to another ring

338

....• (5 indent ) The other ring is alicyclic

339

....•. (6 indent ) Double bonded oxygen, ether or hydroxy, bonded directly to carbon, is attached directly or indirectly to the alicyclic ring by acyclic nonionic bonding (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

340

.... (4 indent ) Sulfur is part of the chain or is attached directly or indirectly to the acyclic carbon or chain by acyclic nonionic bonding with no amino nitrogen between the sulfur and the aryl ring or ring system

341

....• (5 indent ) The sulfur is bonded directly to the aryl ring or ring system

342

.... (4 indent ) Carbonyl is part of the chain or is attached directly or indirectly to the acyclic carbon or chain by acyclic nonionic bonding with no amino nitrogen between the carbonyl and the aryl ring or ring system

343

....• (5 indent ) Processes

344

....• (5 indent ) Hydroxy or ether oxygen bonded directly to the aryl ring or ring system

345

....• (5 indent ) Halogen bonded directly to the aryl ring or ring system

346

.... (4 indent ) Ether oxygen is part of the chain

347

....• (5 indent ) The ether oxygen is bonded directly to the aryl ring or ring system

348

....•. (6 indent ) Hydroxy, bonded directly to carbon, or ether oxygen is attached directly or indirectly to the chain by acyclic nonionic bonding with no amino nitrogen between the hydroxy or attached ether oxygen and the aryl ring or ring system (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

349

....•.. (7 indent ) Alkanol group only between the amino nitrogen and the ether oxygen which is bonded directly to the aryl ring or ring system (i.e., aryloxy alkanol amines)

350

....•... (8 indent ) Nitrogen bonded directly to the aryl ring or ring system

351

....•... (8 indent ) Halogen bonded directly to the aryl ring oring system

352

....•. (6 indent ) The aryl ring or ring system is polycyclo

353

....•. (6 indent ) Hydrogen or acyclic hydrocarbyl substituents only bonded directly to the part of the chain between the ether oxygen and amino nitrogen

354

....•.. (7 indent ) The part of the chain between the ether oxygen and amino nitrogen consists of two unsubstituted saturated carbons

355

.... (4 indent ) Hydroxy, bonded directly to carbon, or ether oxygen attached directly or indirectly to the acyclic carbon or chain by acyclic nonionic bonding with no amino nitrogen between the hydroxy or ether oxygen and the aryl ring or ring system (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

356

....• (5 indent ) Preparing directly by reduction, other than by reductive amination

357

....•. (6 indent ) By direct hydrogenation

358

....•.. (7 indent ) Group VIII noble metal containing catalyst utilized

359

....• (5 indent ) Preparing directly by hydrolysis

360

....• (5 indent ) Additional hydroxy, bonded directly to carbon, or ether oxygen attached directly or indirectly to the acyclic carbon or chain by acyclic nonionic bonding with no amino nitrogen between the additional hydroxy or ether oxygen and the aryl ring or ring system (H of -OH may be replaced by a substituted or unsubstitited ammonium ion or a Group IA or IIA light metal)

361

....• (5 indent ) Plural hydroxy groups bonded directly to the aryl ring or ring system (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

362

....•. (6 indent ) Four or more substituents on the aryl ring or ring system

363

....• (5 indent ) Beta hydroxy phenethylamines (i.e., hydroxy and the benzene ring are bonded directly to the same carbon of the chain which consists of two carbons; H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

364

....•. (6 indent ) Acyclic hydrocarbyl alpha substituent

365

....•. (6 indent ) Hydroxy or ether oxygen bonded directly to the aryl ring or ring system (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

366

.... (4 indent ) Halogen attached directly or indirectly to the acyclic carbon or chain by acyclic nonionic bonding with no amino nitrogen between the halogen and the aryl ring or ring system

367

.... (4 indent ) The chain contains nitrogen between the aryl ring or ring system and amino nitrogen

368

....• (5 indent ) Ethylene diamines

369

....•. (6 indent ) Mono ethylene diamines

370

....•.. (7 indent ) Plural aryl rings, which are not part of the same polycyclo ring system, or ring systems containing

371

....• (5 indent ) Methylene diamines

372

.... (4 indent ) Additional amino nitrogen attached directly or indirectly to the acyclic carbon or chain by acyclic nonionic bonding

373

.... (4 indent ) Alpha aralkyl benzyl amines

374

.... (4 indent ) The chain consists of two or more carbons which are unsubstituted or have acyclic hydrocarbyl substituents only

375

....• (5 indent ) Forming amine group directly by reduction, other than by reductive amination

376

....• (5 indent ) Forming directly by amination which replaces halogen

377

....• (5 indent ) Preparing directly by hydrolysis

378

....• (5 indent ) The aryl ring or ring system is polycyclo

379

....•. (6 indent ) Tricyclo ring system

380

....•.. (7 indent ) The chain contains carbon to carbon unsaturation

381

....• (5 indent ) Phenethylamines having alpha alkyl substituent

382

....• (5 indent ) Phenethylamines having beta alkyl substituent

383

....• (5 indent ) The chain contains carbon to carbon unsaturation

384

.... (4 indent ) The aryl ring or ring system and amino nitrogen are bonded directly to the same acyclic carbon, which carbon additionally has only hydrogen or acyclic hydrocarbyl substituents bonded directly thereto

385

....• (5 indent ) Forming amine group directly by reduction, other than by reductive amination

386

....• (5 indent ) Forming directly by amination which replaces halogen or forming amine group directly by hydrolysis

387

....• (5 indent ) The aryl ring or ring system is polycyclo

388

....• (5 indent ) Plural amino methylene groups bonded directly to the same benzene ring

389

....• (5 indent ) Benzyl amines having hydroxy or ether oxygen bonded directly to the benzene ring (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

390

....•. (6 indent ) Ortho hydroxy benzyl amines

391

....• (5 indent ) Benzyl amines wherein the benzene ring has no other substituents

392

....•. (6 indent ) Acyclic hydrocarbyl group bonded directly to the methylene carbon

393

... (3 indent ) Preparing directly from ester other than by reduction of nitrile

394

... (3 indent ) Preparing directly from organic acid, acid halide or salt

395

... (3 indent ) Preparing directly by amination

396

.... (4 indent ) Of carbonyl containing compound

397

....• (5 indent ) By reductive amination

398

....•. (6 indent ) Group VIII noble metal containing catalyst utilized

399

.... (4 indent ) Of ether or alkylene oxide

400

.... (4 indent ) Of halohydrin

401

.... (4 indent ) Of acyclic hydroxy containing compound

402

.... (4 indent ) By replacing hydroxy

403

....• (5 indent ) In compound having plural hydroxys bonded directly to benzene ring

404

.... (4 indent ) Of halogen containing compound

405

....• (5 indent ) Which also contains benzene ring

406

....•. (6 indent ) And nitro

407

....•. (6 indent ) Preparing primary amines

408

.... (4 indent ) Of hydrocarbon

409

... (3 indent ) Preparing directly by ring alkylation or dealkylaton

410

... (3 indent ) Preparing directly by nitrosation

411

... (3 indent ) Preparing directly by nitration

412

... (3 indent ) Preparing of halogen containing compound directly by halogenation or dehalogenation

413

... (3 indent ) Preparing directly from hetero ring containing compound

414

... (3 indent ) Preparing directly from an amide (e.g., preparing directly from a sulfenamide, nitrosamine, carboxamide, thiourea, etc.)

415

... (3 indent ) Forming amine group directly by reduction

416

.... (4 indent ) Of nitro or nitroso

417

....• (5 indent ) Preparing compound which contains halogen bonded directly to carbon

418

....• (5 indent ) Preparing compound which contains hydroxy, bonded directly to carbon, or ether

419

....• (5 indent ) With initial nitration step

420

....• (5 indent ) By direct hydrogenation

421

....•. (6 indent ) Group VI metal containing catalyst utilized

422

....•. (6 indent ) Group VIII metal containing catalyst utilized

423

....•.. (7 indent ) Group VIII noble metal containing catalyst utilized

424

... (3 indent ) Separating isomers

425

.... (4 indent ) By salt formation

426

... (3 indent ) Polycyclo ring system

427

.... (4 indent ) Tricyclo ring system

428

.... (4 indent ) Bicyclo ring system

429

....• (5 indent ) Naphthyl ring system and benzene ring bonded directly to the same nitrogen

430

... (3 indent ) Two benzene rings bonded directly to the same oxygen, sulfur, or polysulfide chain

431

... (3 indent ) Two carbocyclic rings, at least one of which is benzene, bonded directly to the same nitrogen

432

.... (4 indent ) Condensation products and processes of acyclic ketone and compound which contains two benzene rings bonded directly to the same nitrogen

433

.... (4 indent ) Two benzene rings bonded directly to the same nitrogen

434

....• (5 indent ) Additional amino nitrogen containing

435

....• (5 indent ) Preparing directly by condensing a primary amine

437

... (3 indent ) Purification or recovery

438

.... (4 indent ) By salt formation

439

.... (4 indent ) Of compound having amino nitrogen and hydroxy bonded directly to the benzene ring (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

440

... (3 indent ) Sulfur attached indirectly to the amino nitrogen by nonionic bonding

441

... (3 indent ) Nitro or nitroso, bonded directly to carbon, containing

442

... (3 indent ) Halogen, bonded directly to carbon, containing

443

... (3 indent ) Hydroxy, bonded directly to carbon, or ether containing (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

444

.. (2 indent ) Preparing alicyclic ring containing compound directly by isomerization

445

.. (2 indent ) Preparing alicyclic ring containing compound directly by amination

446

... (3 indent ) Of aldehyde or ketone containing compound

447

... (3 indent ) Of hydroxy containing compound

448

.. (2 indent ) Forming amine group of alicyclic ring containing compound directly by reduction

449

... (3 indent ) Including hydrogenating benzene ring

450

.. (2 indent ) Preparing alicyclic ring containing compound directly by hydrogenating benzene ring

451

... (3 indent ) Plural amino nitrogens containing

452

.. (2 indent ) Plural alicyclic rings, which are not part of the same polycyclo ring system, or ring systems bonded directly to the same carbon

453

.. (2 indent ) Alicyclic ring or ring system and amino nitrogen are attached indirectly by an acyclic carbon or chain

454

... (3 indent ) The chain consists of two or more carbons which are unsubstituted or have acyclic hydrocarbyl substituents only

455

... (3 indent ) The alicyclic ring and amino nitrogen are bonded directly to the same acyclic carbon, which carbon additionally has only hydrogen or acyclic hydrocarbyl substituents bonded directly thereto

456

.... (4 indent ) Polycyclo ring system

457

.. (2 indent ) Plural alicyclic rings

458

... (3 indent ) Polycyclo ring system

459

.... (4 indent ) Tricyclo ring system

460

.... (4 indent ) Bicyclo ring system

461

.. (2 indent ) Alicyclic ring and plural amino nitrogens containing

462

.. (2 indent ) Cyclohexyl ring containing

463

.. (2 indent ) Acyclic

464

... (3 indent ) Aminimine or hydrazine containing

465

.... (4 indent ) Preparing directly by reducing a nitrosamine

466

.... (4 indent ) Preparing directly by condensing a haloamine

467

... (3 indent ) Preparing directly utilizing carbon monoxide

468

... (3 indent ) Preparing directly from ester, organic acid or salt, other than by reduction of nitrile

469

... (3 indent ) Preparing directly by amination

470

.... (4 indent ) By transamination

471

.... (4 indent ) Of aldehyde or ketone containing compound

472

....• (5 indent ) By reductive amination

473

....•. (6 indent ) Of aldehyde containing compound

474

.... (4 indent ) Of ether containing compound

475

....• (5 indent ) Of an alkylene oxide

476

....•. (6 indent ) Of an epihalohydrin

477

....•. (6 indent ) Producing monohydroxy alkyl amines

478

.... (4 indent ) Of hydroxy containing compound

479

....• (5 indent ) Catalyst utilized

480

....•. (6 indent ) Group VI or VIII metal containing catalyst utilized

481

.... (4 indent ) Of halogen containing compound

482

....• (5 indent ) Of an alkylene dihalide

483

....• (5 indent ) Of compound which contains an atom other than carbon, hydrogen, and halogen

484

....• (5 indent ) Of compound which contains carbon to carbon unsaturation

485

.... (4 indent ) Of compound which contains carbon to carbon unsaturation

486

... (3 indent ) Preparing directly by dealkylation

487

... (3 indent ) Preparing directly from hetero ring containing compound

488

... (3 indent ) Preparing directly from an amide (e.g., preparing directly from a carboxamide, etc.)

489

... (3 indent ) Forming amine group directly by reduction

490

.... (4 indent ) Of cyano

491

....• (5 indent ) Of plural cyanos

492

....•. (6 indent ) Preparing hexamethylene diamine

493

....• (5 indent ) Preparing a primary monoamine

494

.... (4 indent ) Of nitro or nitroso

495

....• (5 indent ) The nitro or nitroso is in a compound which contains hydroxy, bonded directly to carbon, or ether

496

... (3 indent ) Preparing directly by halogenation

497

... (3 indent ) Purification or recovery

498

.... (4 indent ) Of an alkylene polyamine

499

.... (4 indent ) Separating primary, secondary, or tertiary amines from each other

500

... (3 indent ) Sulfur attached indirectly to the amino nitrogen by nonionic bonding

501

.... (4 indent ) Thioether containing

502

... (3 indent ) Aldehyde or ketone containing

503

... (3 indent ) Hydroxy, bonded directly to carbon, or ether containing (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

504

.... (4 indent ) Polyether

505

....• (5 indent ) Polyoxyalkylene

506

.... (4 indent ) Polyhydroxy (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

507

....• (5 indent ) Plural hydroxys in the same substituent on the amino nitrogen (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)

508

.... (4 indent ) Monoether

509

... (3 indent ) Carbon to carbon unsaturation containing

510

... (3 indent ) Halogen, bonded directly to carbon, containing

511

... (3 indent ) Plural amino nitrogens containing

512

.... (4 indent ) Three or more amino nitrogens containing

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