IPC 7 English version C07C 43/00-C07C 45/90

IPC ⁷ English version

C07C 37/00 - C07C 41/60

C07C04300-C07C04590

C07C 46/00 - C07C 49/92

SECTION C – CHEMISTRY; METALLURGY

C 07

ORGANIC CHEMISTRY (such compounds as the oxides, sulfides, or oxysulfides of carbon, cyanogen, phosgene, hydrocyanic acid or salts thereof C01; products obtained from layered base-exchange silicates by ion-exchange with organic compounds such as ammonium, phosphonium or sulfonium compounds or by intercalation of organic compounds C01B 33/44; macromolecular compounds C08; dyes C09; fermentation products C12; fermentation or enzyme-using processes to synthesise a desired chemical compound or composition or to separate optical isomers from a racemic mixture C12P; production of organic compounds by electrolysis or electrophoresis C25B 3/00, C25B 7/00) [2]

C 07 C

ACYCLIC OR CARBOCYCLIC COMPOUNDS

43/

Ethers; Compounds having groups, groups or groups

43/

Ethers

43/

having all ether-oxygen atoms bound to acyclic carbon atoms [3]

43/

Saturated ethers [3]

43/

Diethyl ether [3]

43/

of polyhydroxy compounds [3]

43/

Polyethers containing –O–(C–C–O–)_n units with 2 >= n >= 10 [2,3]

43/

115

containing carbocyclic rings [3]

43/

containing halogen [3]

43/

containing hydroxy or O-metal groups (C07C 43/11 takes precedence) [3]

43/

Unsaturated ethers [3]

43/

containing only non-aromatic carbon-to-carbon double bonds [3]

43/

Vinyl ethers [3]

43/

162

containing rings other than six-membered aromatic rings [3]

43/

164

containing six-membered aromatic rings [3]

43/

166

having unsaturation outside the aromatic rings [3]

43/

168

containing six-membered aromatic rings and other rings [3]

43/

containing halogen [2,3]

43/

172

containing rings other than six-membered aromatic rings [3]

43/

174

containing six-membered aromatic rings [3]

43/

176

having unsaturation outside the aromatic rings [3]

43/

178

containing hydroxy or O-metal groups [3]

43/

having an ether-oxygen atom bound to a carbon atom of a ring other than a six-membered aromatic ring

43/

184

to a carbon atom of a non-condensed ring [3]

43/

188

Unsaturated ethers [3]

43/

192

containing halogen [3]

43/

196

containing hydroxy or O-metal groups [3]

43/

having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring

43/

205

the aromatic ring being a non-condensed ring [3]

43/

containing rings other than six-membered aromatic rings [3]

43/

215

having unsaturation outside the six-membered aromatic rings [3]

43/

225

containing halogen [3]

43/

containing hydroxy or O-metal groups [3]

43/

235

having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring and to a carbon atom of a ring, other than a six-membered aromatic ring [3]

43/

243

having unsaturation outside the six-membered aromatic rings [3]

43/

247

containing halogen [3]

43/

253

containing hydroxy or O-metal groups [3]

43/

257

having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings [3]

43/

263

the aromatic rings being non-condensed [3]

43/

267

containing other rings [3]

43/

275

having all ether-oxygen atoms bound to carbon atoms of six-membered aromatic rings [3]

43/

285

having unsaturation outside the six-membered aromatic rings [3]

43/

containing halogen [3]

43/

295

containing hydroxy or O-metal groups [3]

43/

Compounds having

groups

Note

In this group, the acetal carbon atom is the carbon of the

group. [3]

43/

303

having acetal carbon atoms bound to acyclic carbon atoms [3]

43/

305

having acetal carbon atoms as ring members or bound to carbon atoms of rings other than six-membered aromatic rings [3]

43/

307

having acetal carbon atoms bound to carbon atoms of six-membered aromatic rings [3]

43/

313

containing halogen [3]

43/

315

containing oxygen atoms singly bound to carbon atoms not being acetal carbon atoms [3]

43/

317

having

groups, X being hydrogen or metal [3]

43/

Compounds having

groups or

groups

45/

Preparation of compounds having C=O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds [2]

45/

by hydration of carbon-to-carbon triple bonds [3]

45/

by oxidation (with ozone C07C 45/40) [3]

45/

of –CH_x-moieties [3]

45/

of hydroxy groups [3]

45/

with halogen containing compounds, e.g. hypohalogenation [3]

45/

with compounds containing mercury atoms, which may be regenerated in situ, e.g. by oxygen [3]

45/

with molecular oxygen [3]

45/

of CH_x-moieties [3]

45/

in unsaturated compounds [3]

45/

in propene or isobutene [3]

45/

in compounds containing six-membered aromatic rings [3]

45/

C–O– functional groups to

C=O groups [3]

45/

being a primary hydroxy group [3]

45/

being a secondary hydroxy group [3]

45/

by oxidation with ozone; by ozonolysis [3]

45/

by hydrogenolysis or reduction of carboxylic groups or functional derivatives thereof [3]

45/

by hydrolysis [3]

45/

CX₂ groups, X being halogen [3]

45/

by reduction and hydrolysis of nitriles [3]

45/

by condensation [3]

45/

Friedel-Crafts reactions [3]

45/

using phosgene [3]

45/

involving decarboxylation [3]

45/

by reaction with carbon monoxide [3]

45/

by oxo-reactions [3]

45/

by pyrolysis, rearrangement or decomposition [3]

45/

by dehydration and rearrangement involving two hydroxy groups in the same molecule [3]

45/

of hydroperoxides [3]

45/

of compounds containing doubly bound oxygen atoms, e.g. esters [3]

45/

of oligo- or polymeric oxo-compounds [3]

45/

from heterocyclic compounds (C07C 45/55 takes precedence) [3]

45/

with oxygen as the only hetero atom [3]

45/

in three-membered rings [3]

45/

in five-membered rings (from ozonides C07C 45/40) [3]

45/

in six-membered rings [3]

45/

by reactions not involving the formation of

C=O groups [3]

45/

by hydrogenation of carbon-to-carbon double or triple bonds [3]

45/

by introduction of halogen; by substitution of halogen atoms by other halogen atoms [3]

45/

by introduction of functional groups containing oxygen only in singly bound form [3]

45/

by splitting-off hydrogen atoms or functional groups; by hydrogenolysis of functional groups [3]

45/

by dehydration [3]

45/

by isomerisation; by change of size of the carbon skeleton [3]

45/

by increase in the number of carbon atoms [3]

45/

by addition to carbon-to-carbon double or triple bonds [3]

45/

by reaction with functional groups containing oxygen only in singly bound form [3]

45/

being hydroxy groups [3]

45/

by reaction of compounds containing

C=O groups with the same or other compounds containing

C=O groups [3]

45/

combined with hydrogenation [3]

45/

combined with dehydration [3]

45/

Reactions with formaldehyde [3]

45/

with the aid of ketenes [3]

45/

Preparation of chelates of aldehydes or ketones [3]

45/

Separation; Purification; Stabilisation; Use of additives [3]

45/

by solid-liquid treatment; by chemisorption [3]

45/

by liquid-liquid treatment [3]

45/

by change in the physical state, e.g. crystallisation [3]

45/

by distillation [3]

45/

by extractive distillation [3]

45/

by azeotropic distillation [3]

45/

by treatment giving rise to a chemical modification (by chemisorption C07C 45/79) [3]

45/

Use of additives, e.g. for stabilisation [3]

45/

Preparation of ketenes or dimeric ketenes (heterocyclic compounds C07D) [3]

45/

from ketones [3]

45/

from carboxylic acids, their anhydrides, esters or halides [3]

45/

Separation; Purification; Stabilisation; Use of additives [3]

C07C 37/00 - C07C 41/60

C07C 46/00 - C07C 49/92