Class   560	ORGANIC COMPOUNDS -- PART OF THE CLASS 532-570 SERIES
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This Class 560 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 ) Carboxylic acid esters

2

.. (2 indent ) With preservative

3

... (3 indent ) Aromatic polycarboxylic acid esters

4

... (3 indent ) Acyclic unsaturated monocarboxylic acid esters

5

.. (2 indent ) Hydrophenanthrene in acid moiety

6

... (3 indent ) Polycyclo ring system having the hydrophenanthrene and at least one additional ring as cyclos

7

... (3 indent ) 1,4a-Dimethylhydrophenanthrene-1- carboxylic acid

8

.. (2 indent ) Aromatic acid moiety

9

... (3 indent ) Sulfur in acid moiety

10

.... (4 indent ) Ortho fused rings in acid moiety

11

.... (4 indent ) Sulfoxy in acid moiety

12

....• (5 indent ) Nitrogen in acid moiety

13

....•. (6 indent ) Plural nitrogens in acid moiety

14

....• (5 indent ) Sulfonic acids, salts or acid halides

15

.... (4 indent ) Sulfur, not bonded directly to a ring, in same side chain as ester function

16

....• (5 indent ) Nitrogen in acid moiety

17

.... (4 indent ) Sulfur, bonded directly to a ring, in same side chain as ester function

18

.... (4 indent ) Ester function attached directly to a ring

19

... (3 indent ) Nitrogen in acid moiety other than as nitroso or isocyanate (e.g., amino acid esters, etc.)

20

.... (4 indent ) Nitro bonded to carbon in acid moiety

21

....• (5 indent ) Plural rings in acid moiety

22

....• (5 indent ) Additional nitrogen in acid moiety

23

....• (5 indent ) Oxy, aldehyde or ketone group in acid moiety

24

.... (4 indent ) Carbamic acid

25

....• (5 indent ) Polycarbamic

26

....•. (6 indent ) Polyoxy alcohol moiety

27

....• (5 indent ) Plural rings in acid moiety

28

....•. (6 indent ) Ortho fused

29

....• (5 indent ) Oxy in acid moiety

30

....• (5 indent ) Halogen in acid moiety

31

....•. (6 indent ) Ring in alcohol moiety

32

....• (5 indent ) Ring in alcohol moiety

33

....• (5 indent ) Sulfur, nitrogen, halogen or additional oxy in alcohol moiety

34

.... (4 indent ) Ureido, guanido or hydrazino in acid moiety

35

.... (4 indent ) Amidine, azomethine, ketimine or oxime in acid moiety

36

.... (4 indent ) Plural rings bonded directly to the same cyclic carbon in acid moiety

37

.... (4 indent ) The nitrogen is not bonded directly to a ring

38

....• (5 indent ) The nitrogen is in same side chain as ester function

39

....•. (6 indent ) Oxy in acid moiety

40

....•.. (7 indent ) Phenylalanines

41

....•. (6 indent ) Amide in acid moiety

42

....• (5 indent ) Oxy in acid moiety

43

.... (4 indent ) The nitrogen is bonded directly to a ring and is in same side chain as ester function

44

....• (5 indent ) Polycarboxylic acid

45

.... (4 indent ) Oxy in acid moiety

46

....• (5 indent ) Benzoic acid substituted on ring with oxy and nitrogen

47

.... (4 indent ) Halogen in acid moiety

48

.... (4 indent ) Plural rings in acid moiety with nitrogen bonded directly to at least one of the rings

49

.... (4 indent ) Nitrogen in alcohol moiety

50

.... (4 indent ) Polyoxy alcohol moiety

51

... (3 indent ) Aldehyde or ketone group in acid moiety

52

.... (4 indent ) Plural rings bonded directly to the same carbonyl in acid moiety

53

.... (4 indent ) Oxy in acid moiety

54

.... (4 indent ) Polycarboxylic acid

55

... (3 indent ) Oxy in acid moiety

56

.... (4 indent ) Ortho fused rings in acid moiety

57

.... (4 indent ) Plural rings bonded directly to the same acyclic carbon in acid moiety

58

....• (5 indent ) Nitrogen in alcohol moiety

59

.... (4 indent ) Rings bonded directly to each other in acid moiety

60

.... (4 indent ) Oxy, not bonded directly to a ring, in same side chain as ester function

61

.... (4 indent ) Oxy, bonded directly to a ring, in same side chain as ester function

62

....• (5 indent ) Halogen in acid moiety

63

....•. (6 indent ) Polyoxy alcohol moiety

64

.... (4 indent ) Ester function attached directly to a ring

65

....• (5 indent ) Halogen in acid moiety

66

....• (5 indent ) Acylated

67

....• (5 indent ) Phenolic hydroxy or metallate

68

....•. (6 indent ) Tannins and reaction products thereof

69

....•.. (7 indent ) Extraction from bark or vegetable material

70

....•. (6 indent ) Polyphenolic hydroxy or metallate

71

....•. (6 indent ) Salicylic acid

72

....•. (6 indent ) Ring in alcohol moiety

73

....• (5 indent ) Ring in alcohol moiety

74

....• (5 indent ) Nitrogen in alcohol moiety

75

.... (4 indent ) Phenolic hydroxy or metallate

76

... (3 indent ) Polycarboxylic acid

77

.... (4 indent ) Producing carboxyl group by oxidation

78

.... (4 indent ) Purification or recovery

79

....• (5 indent ) Of ester of polyoxy alcohols

80

.... (4 indent ) Ortho fused rings in acid moiety

81

.... (4 indent ) Esterified carboxy not bonded directly to a ring

82

....• (5 indent ) Malonates

83

.... (4 indent ) Halogen in acid moiety

84

.... (4 indent ) Ring in alcohol moiety

85

....• (5 indent ) Aromatic alcohol moiety

86

....•. (6 indent ) Esterified phenolic hydroxy

87

.... (4 indent ) Sulfur or halogen in alcohol moiety

88

.... (4 indent ) Nitrogen in alcohol moiety

89

.... (4 indent ) Polyoxy alcohol moiety

90

....• (5 indent ) Additional esterifying acid

91

....• (5 indent ) Polyoxyalkylene alcohol moiety

92

....• (5 indent ) Preparing esters by ester interchange

93

....• (5 indent ) Preparing esters from alkylene oxides

94

....• (5 indent ) Preparing esters from acid or from nitrile and diol

95

.... (4 indent ) Unsaturation in alcohol moiety

96

.... (4 indent ) Processes

97

....• (5 indent ) Carbonylation

98

....• (5 indent ) Esterification of acid, salt, acid halide or anhydride with alcohol

99

....•. (6 indent ) Metal containing catalyst utilized

100

... (3 indent ) Naphthyl in acid moiety

101

... (3 indent ) Plural rings bonded directly to the same carbon in acid moiety

102

... (3 indent ) Rings bonded directly to each other in acid moiety

103

... (3 indent ) Monocyclic acid moiety

104

.... (4 indent ) Additional unsaturation in acid moiety

105

.... (4 indent ) Carboxyl, not bonded directly to a ring, in acid moiety

106

.... (4 indent ) Ring in alcohol moiety

107

....• (5 indent ) Plural rings in alcohol moiety

108

....•. (6 indent ) Esterified phenolic hydroxy

109

....• (5 indent ) Esterified phenolic hydroxy

110

.... (4 indent ) Nitrogen in alcohol moiety

111

.... (4 indent ) Halogen in alcohol moiety

112

.... (4 indent ) Polyoxy alcohol moiety

113

.... (4 indent ) Unsaturation in alcohol moiety

114

.. (2 indent ) Preparing alicyclic acid esters by carbonylation

115

.. (2 indent ) Alicyclic carbamates

116

.. (2 indent ) Plural alicyclic rings in acid moiety

117

... (3 indent ) Tricyclo ring system in acid moiety

118

... (3 indent ) Two rings only in acid moiety

119

.... (4 indent ) Ortho fused

120

.... (4 indent ) 2,2,1-bicyclo

121

.. (2 indent ) Cyclopentyl in acid moiety (e.g., prostaglandins, etc.)

122

... (3 indent ) Cyclopentyl-COOR, -C-COOR or -C-C-COOR

123

.. (2 indent ) Cyclobutyl in acid moiety

124

.. (2 indent ) Cyclopropyl in acid moiety

125

.. (2 indent ) Alicyclic acid moiety containing N, S, P, B or halogen

126

.. (2 indent ) Alicyclic acid moiety containing oxy, aldehyde or ketone group

127

.. (2 indent ) Alicyclic polycarboxylic acid moiety

128

.. (2 indent ) Alicyclic acid moiety containing unsaturation

129

.. (2 indent ) Acyclic acid moiety

130

... (3 indent ) Esterified phenolic hydroxy

131

.... (4 indent ) Preparing esters by oxidation

132

.... (4 indent ) Carbamic acid

133

....• (5 indent ) Plural rings in phenolic moiety

134

....•. (6 indent ) Ortho fused

135

....• (5 indent ) Sulfur in phenolic moiety

136

....• (5 indent ) Nitrogen in phenolic moiety

137

....• (5 indent ) Sulfur, halogen or additional nitrogen or oxygen in carbamic acid moiety

138

.... (4 indent ) Plural rings in phenolic moiety

139

....• (5 indent ) Ortho fused

140

....• (5 indent ) Plural rings bonded directly to the same carbon in phenolic moiety

141

....• (5 indent ) Rings bonded directly to each other in phenolic moiety

142

.... (4 indent ) Nitrogen or sulfur in phenolic moiety

143

.... (4 indent ) Salicylic acid or functional derivative

144

.... (4 indent ) Polyoxy phenolic moiety

145

.... (4 indent ) Sulfur, nitrogen, halogen, oxy, or aldehyde or ketone group in acid moiety

146

.... (4 indent ) Polycarboxylic acid

147

... (3 indent ) Sulfur in acid moiety

148

.... (4 indent ) Carbamic acid

149

.... (4 indent ) Sulfoxy in acid moiety

150

....• (5 indent ) Sulfonyl or sulfinyl in acid moiety

151

....• (5 indent ) Polycarboxylic acid

152

.... (4 indent ) Thio ether in acid moiety

153

....• (5 indent ) Nitrogen or halogen in acid moiety

154

....• (5 indent ) Polycarboxylic acid

155

... (3 indent ) Nitrogen in acid moiety other than as nitroso or isocyanate (e.g., amino acid esters, etc.)

156

.... (4 indent ) Nitro bonded to carbon in acid moiety

157

.... (4 indent ) Carbamic acid

158

....• (5 indent ) Polycarbamic

159

....• (5 indent ) Additional nitrogen in acid moiety

160

....• (5 indent ) Oxy in acid moiety

161

....• (5 indent ) Halogen in acid moiety

162

....• (5 indent ) Cyclic alcohol moiety

163

....•. (6 indent ) Aromatic alcohol moiety

164

....•.. (7 indent ) Polyoxy alcohol moiety

165

....• (5 indent ) Sulfur or nitrogen in alcohol moiety

166

....• (5 indent ) Polyoxy alcohol moiety

167

....• (5 indent ) Halogen in alcohol moiety

168

.... (4 indent ) Amidine, azomethine, ketimine or oxime in acid moiety

169

.... (4 indent ) Additional nitrogen in acid moiety

170

.... (4 indent ) Oxy, aldehyde or ketone group in acid moiety

171

.... (4 indent ) Polycarboxylic acid

172

.... (4 indent ) Halogen or unsaturation in acid moiety

173

.... (4 indent ) Cyclic alcohol moiety

174

... (3 indent ) Aldehyde or ketone group in acid moiety

175

.... (4 indent ) Preparing esters by carbonylation

176

.... (4 indent ) Polycarboxylic acid

177

.... (4 indent ) Aldehyde group in acid moiety

178

.... (4 indent ) Acetoacetic acid

179

... (3 indent ) Oxy in acid moiety

180

.... (4 indent ) Polycarboxylic acid

181

....• (5 indent ) Unsaturation in acid moiety

182

....• (5 indent ) Polyoxy alcohol moiety

183

.... (4 indent ) Unsaturation in acid moiety

184

.... (4 indent ) Halogen in acid moiety

185

.... (4 indent ) Acylated oxy in acid moiety

186

.... (4 indent ) Polyoxy acid moiety

187

.... (4 indent ) Alkoxy in acid moiety

188

.... (4 indent ) Cyclic alcohol moiety

189

.... (4 indent ) Polyoxy alcohol moiety

190

... (3 indent ) Polycarboxylic acid

191

.... (4 indent ) Purification or recovery

192

.... (4 indent ) Halogen in acid moiety

193

.... (4 indent ) Cyclic alcohol moiety

194

....• (5 indent ) Plural rings in alcohol moiety

195

.... (4 indent ) Phosphorus or sulfur in alcohol moiety

196

.... (4 indent ) Nitrogen in alcohol moiety

197

.... (4 indent ) Halogen in alcohol moiety

198

.... (4 indent ) Polyoxy alcohol moiety

199

....• (5 indent ) Additional monooxy alcohol or monocarboxylic acid (e.g., complex esters, etc.)

200

....• (5 indent ) Preparing esters from alkylene oxides

201

.... (4 indent ) Unsaturation in alcohol moiety

202

.... (4 indent ) Preparing esters by oligomerization

203

.... (4 indent ) Preparing esters by alkylation or isomerization

204

.... (4 indent ) Preparing esters by esterification or carbonylation

205

... (3 indent ) Unsaturation in acid moiety

206

.... (4 indent ) Preparing esters by carbonylation

207

....• (5 indent ) Group VIII noble metal catalyst utilized

208

.... (4 indent ) Formation of carboxyl group by oxidation

209

.... (4 indent ) Preparing esters from alkylene oxides

210

.... (4 indent ) Preparing esters from aldehydes

211

.... (4 indent ) Formation of ethylenic unsaturation

212

....• (5 indent ) By dehydration or dealcoholization

213

....• (5 indent ) By dehalogenation or dehydrohalogenation

214

....• (5 indent ) By dehydrogenation

215

.... (4 indent ) Preparing esters from nitriles or amides

216

.... (4 indent ) Preparing esters by depolymerization

217

.... (4 indent ) Preparing esters by ester interchange

218

.... (4 indent ) Purification or recovery

219

.... (4 indent ) Halogen in acid moiety

220

.... (4 indent ) Cyclic alcohol moiety

221

....• (5 indent ) Aromatic alcohol moiety

222

.... (4 indent ) Phosphorus, sulfur or nitrogen in alcohol moiety

223

.... (4 indent ) Halogen in alcohol moiety

224

.... (4 indent ) Polyoxy alcohol moiety

225

.... (4 indent ) Unsaturation in alcohol moiety

226

... (3 indent ) Halogen in acid moiety

227

.... (4 indent ) Fluorine in acid moiety

228

.... (4 indent ) Cyclic alcohol moiety

229

.... (4 indent ) Halogen in alcohol moiety

230

.... (4 indent ) Polyoxy alcohol moiety

231

... (3 indent ) Unsubstituted acids of the acetic series

232

.... (4 indent ) Preparing esters by carbonylation

233

....• (5 indent ) Of olefins

234

.... (4 indent ) Preparing esters by ester interchange

235

....• (5 indent ) From alkyl sulfates

236

.... (4 indent ) Preparing esters from halogenated hydrocarbons

237

....• (5 indent ) From alkenyl halides

238

.... (4 indent ) Preparing esters from aldehydes

239

.... (4 indent ) Preparing esters by dehydrogenation of alcohols

240

.... (4 indent ) Preparing esters from ethers

241

.... (4 indent ) Preparing esters from hydrocarbons

241.1

....• (5 indent ) By oxidation of hydrocarbon mixtures

242

....• (5 indent ) From acetylenic hydrocarbons

243

....• (5 indent ) From olefins utilizing Group VIII noble metal catalyst

244

....•. (6 indent ) From polyolefins

245

....•. (6 indent ) Gas phase

246

....• (5 indent ) Preparing polyoxy alcohol esters from olefins

247

....• (5 indent ) Preparing alkyl esters from olefins

248

.... (4 indent ) Purification or recovery

249

.... (4 indent ) Terpene alcohol moiety

250

.... (4 indent ) Nitrogen in alcohol moiety other than as nitro, nitroso or isocyanate

251

....• (5 indent ) Plural nitrogens in alcohol moiety

252

....• (5 indent ) Polyoxy alcohol moiety

253

....• (5 indent ) Acyclic alcohol moiety

254

.... (4 indent ) Aromatic alcohol moiety

255

....• (5 indent ) Plural rings in alcohol moiety

256

.... (4 indent ) Polycyclo-alicyclic ring system in alcohol moiety

257

....• (5 indent ) Nor- or homo- cyclopentanohydrophenanthrenes

258

....•. (6 indent ) Nor-A ring

259

.... (4 indent ) 2,6,6-trialkyl cyclohexenyl in alcohol moiety

260

....• (5 indent ) Vitamin A alcohol moiety

261

.... (4 indent ) Acyclic alcohol moiety having unsaturation

262

....• (5 indent ) Substituted

263

.... (4 indent ) Acyclic polyoxy alcohol moiety

264

....• (5 indent ) Substituted

265

.... (4 indent ) Acyclic monohydric alcohol moiety

266

....• (5 indent ) Substituted

300

. (1 indent ) Hypohalite or perhypohalite esters (i.e., compounds having the -O-halo group or the -O-O-halo group bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon)

301

. (1 indent ) Cyanate esters (i.e., compounds having the -OCN group bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon)

302

. (1 indent ) Compounds having the group -C(=X)-X-nX-, wherein the X's may be the same or diverse chalcogens, nX is a divalent chalcogen or a chain of divalent chalcogens single bonded to each other, and the terminal X is bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon (e.g., percarboxylate esters, etc.)

303

. (1 indent ) Sulfohydroxamate esters or chalcogen analogues thereof (i.e., compounds having the -S(=O)(=O)-NH-X- group, wherein X is chalcogen and substitution may be made for hydrogen only, and wherein the X is bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon)

304

. (1 indent ) Peroxynitrate esters (i.e., compounds having the -O-O-N(=O)(=O) group bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon)

305

. (1 indent ) Perborate esters or chalcogen analogues thereof (i.e., compounds having the -X-X- group, wherein the X's are the same or diverse chalcogens, bonded directly to boron and to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon)

306

. (1 indent ) Perhalate esters (i.e., compounds having the -O-halo(=O)(=O)(=O) group bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon)

307

. (1 indent ) Esters having the -S(=O)(=O)-S- group, wherein the divalent sulfur is bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon (e.g., thiolsulfonate esters, etc.)

308

.. (2 indent ) Oxygen bonded directly to the hexavalent sulfur of the -S(=O)(=O)-S- group (i.e., thiosulfate esters)

309

... (3 indent ) Nitrogen attached indirectly to the -S(=O)(=O)-S- group by acyclic nonionic bonding

310

. (1 indent ) Esters having the -S(=O)-S- group, wherein the divalent sulfur is bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon (e.g., thiolsulfinate esters, dithiosulfurous acid esters, etc.)

311

. (1 indent ) Perhydroxamate esters or chalcogen analogues thereof (i.e., compounds having the -C(=X)-NH-X-X- group, wherein the X's are the same or diverse chalcogens and substitution may be made for hydrogen only, and wherein the terminal X is bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon)

312

. (1 indent ) Hydroxamate esters or chalcogen analogues thereof (i.e., compounds having the -C(=X)-NH-X- group, wherein the X's may be the same or diverse chalcogens and substitution may be made for hydrogen only, and wherein the single bonded X is bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon)

313

.. (2 indent ) Nitrogen bonded directly to the carbon of the -C(=X)-NH-X- group

314

... (3 indent ) The single bonded X is sulfur, or the substituent nitrogen is bonded directly to acyclic or alicyclic carbon

315

.. (2 indent ) Carbocyclic ring bonded directly to the carbon of the -C(=X)-NH-X- group

316

. (1 indent ) Hyponitrite esters (i.e., compounds having the -O-N=N-O- group bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon)

317

. (1 indent ) Esters having the -N=S=O group bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon (i.e., sulfinylamines)

318

. (1 indent ) Persulfonate esters (i.e., compounds having the -S(=O)(=O)-O-O- group, wherein the terminal oxygen is bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon)

319

. (1 indent ) Perthioimidate esters (i.e., compounds having the perthioimidate group, HN=CH-S-S-, wherein substitution may be made for hydrogen only, bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon)

330

. (1 indent ) Isocyanate esters (i.e., compounds containing the isocyanate group, -N=C=O, bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon)

331

.. (2 indent ) With preservative or stabilizer

332

... (3 indent ) Nitrogen containing preservative or stabilizer

333

... (3 indent ) Phosphorus, silicon, or phenolic hydroxy containing preservative or stabilizer

334

.. (2 indent ) Carbodiimide containing (i.e., -N=C=N- containing)

335

.. (2 indent ) Biuret containing (i.e., -NH-C(=O)-NH-C(=O)-NH- containing, wherein substitution may be made for hydrogen only)

336

.. (2 indent ) Processes

337

... (3 indent ) Isocyanic acid, or salt thereof, as reactant

338

... (3 indent ) Processes for forming the isocyanate group

339

.... (4 indent ) Cyanate reactant (i.e., reactant contains -OCN group)

340

.... (4 indent ) Hetero ring containing reactant

341

.... (4 indent ) Carbon monoxide utilized

342

....• (5 indent ) Reactant contains nitro group bonded directly to carbon

343

.... (4 indent ) Azide reactant (i.e., reactant contains the azide group)

344

.... (4 indent ) Reactant containing -NH-C(=O)-NH- group (wherein substitution may be made for hydrogen only)

345

.... (4 indent ) Carbamate reactant (i.e., reactant contains -O-C(=O)-NH- group (wherein substitution may be made for hydrogen only)

346

.... (4 indent ) Reactant containing nitrogen double or triple bonded to carbon (e.g., nitriles, isonitriles, cyanogen halides, etc.)

347

.... (4 indent ) Carbonyl dihalide reactant (e.g., phosgene, etc.)

348

.... (4 indent ) Carbamyl halide reactant (i.e., reactant contains halo-C(=O)-NH- group, wherein substitutuion may be made for hydrogen only)

349

... (3 indent ) Halogenation of isocyanate esters

350

... (3 indent ) Isocyanate exchange reactions (i.e., A-NCO + B-X = B-NCO + A-X)

351

... (3 indent ) Processes of reacting isocyanate esters of known structure to yield products of indeterminate structure

352

... (3 indent ) Purification or recovery

353

.... (4 indent ) Epoxy compound, or metal, utilized

354

.. (2 indent ) Containing polycyclo ring system having alicyclic ring as one of the cyclos

355

.. (2 indent ) Acyclic carbon bonded directly to the isocyanate group

356

... (3 indent ) Halogen attached indirectly to the isocyanate group by acyclic nonionic bonding

357

... (3 indent ) Chalcogen, single bonded directly to carbon, attached indirectly to the isocyanate group by acyclic nonionic bonding (e.g., ether group containing, etc.)

358

.. (2 indent ) Benzene ring bonded directly to the isocyanate group

359

... (3 indent ) Plural benzene rings bonded directly to isocyanate groups (e.g., diisocyanatodiphenylmethane, etc.)

360

... (3 indent ) Plural isocyanate groups bonded directly to the same benzene ring

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