93740-32-0

Basic information

• Product Name: ester methylique de l'acide cis-p-anisoyl-3 trimethyl-1,2,2 cyclopentane carboxylique
• CAS NO: 93740-32-0
• Molecular Weight: 304.386
• Mol File: 93740-32-0.mol

Chemical Properties

• CAS DataBase Reference: ester methylique de l'acide cis-p-anisoyl-3 trimethyl-1,2,2 cyclopentane carboxylique(CAS DataBase Reference)
• NIST Chemistry Reference: ester methylique de l'acide cis-p-anisoyl-3 trimethyl-1,2,2 cyclopentane carboxylique(93740-32-0)
• EPA Substance Registry System: ester methylique de l'acide cis-p-anisoyl-3 trimethyl-1,2,2 cyclopentane carboxylique(93740-32-0)

Safety Data

• Hazardous Substances Data: 93740-32-0(Hazardous Substances Data)

Upstream product

• 186581-53-3 diazomethane 
• 145415-55-0 acide (-)-cis-p-anisoyl-3 trimethyl-1,2,2 cyclopentane carboxylique 
• 100-66-3 methoxybenzene 
• 93740-34-2 (1S,3R)-3-Chlorocarbonyl-1,2,2-trimethyl-cyclopentanecarboxylic acid methyl ester 
• 560-09-8 (1S,3R)-(-)-camphoric acid 
• 145415-56-1 acide (-)-trans-p-anisoyl-3 trimethyl-1,2,2 cyclopentane carboxylique 
• 560-07-6 (1S,3S)-(+)-1,2,2-trimethylcyclopentane-1,3-dicarboxylic acid 
• 57078-08-7 acide cis-p-anisoyl-3 trimethyl-1,2,2 cyclopentane carboxylique 
• 76-32-4 (±)-camphoric acid anhydride 
• 595-31-3 (+)-(1S,3R)-1,2,2-trimethylcyclopentane-1,3-dicarboxylic anhydride 
• 7282-27-1 (1S,3S)-1,2,2-Trimethyl-cyclopentane-1,3-dicarboxylic acid dimethyl ester 
• 26252-16-4 (1S,3S)-1,2,2-Trimethyl-cyclopentane-1,3-dicarboxylic acid 1-methyl ester 
• 100938-20-3 (1S,3S)-3-Chlorocarbonyl-1,2,2-trimethyl-cyclopentanecarboxylic acid methyl ester 
• 7282-27-1 (1S,3R)-dimethyl 1,2,2-trimethylcyclopentane-1,3-dicarboxylate 

Downstream Products

• 122082-34-2 (1S,3R)-3-[[(E)-Hydroxyimino]-(4-methoxy-phenyl)-methyl]-1,2,2-trimethyl-cyclopentanecarboxylic acid methyl ester 
• 122082-75-1 chlorhydrate d'(α-dimethylamino methoxy-4 benzyl)-3 trimethyl-1,2,2 cyclopentane methanol-1 
• 122082-73-9 chlorhydrate d'(α-methylamino methoxy-4 benzyl)-3 trimethyl-1,2,2 cyclopentane methanol-1 
• 122082-45-5 (1R,6S)-5-(4-Methoxy-phenyl)-1,9,9-trimethyl-3-oxa-4-aza-bicyclo[4.2.1]nonane; hydrochloride 
• 122082-71-7 <α-(N-benzyloxycarbonyl N-methyl amino) methoxy-4 benzyl>-3 trimethyl-1,2,2 cyclopentane carboxylate de methyle 
• 122082-70-6 <α-(N-benzyloxycarbonyl amino) p-methoxy benzyl>-3 trimethyl-1,2,2 cyclopentane carboxylate de methyle 
• 122082-72-8 (α-methylamino methoxy-4 benzyl)-3 trimethyl-1,2,2 cyclopentane carboxylate de methyle 
• 122082-67-1 (α-amino p-methoxy benzyl)-3 trimethyl-1,2,2 cyclopentane carboxylate de methyle 

Relevant articles and documents

Synthese et activites myocardiques d'(α-amino aryl methyl)-3 trimethyl-1,2,2 cyclopentane methanol-1 et de leurs analogues cycliques oxazepiniques

The synthesis of 3-(α-amino aryl methyl)-1,2,2-trimethyl-cyclopentane-1-methanol and of heterocyclic analogues 5-aryl-1,9,9-trimethyl-3-oxa-4-azabicyclononane, substituted in the aromatic ring, is described.These derivatives are obtained from 3-ary

Reaction de l'anhydride camphorique sur differents composes aromatiques (Friedel Crafts) I. Etude des isomeres structuraux et des stereoisomeres obtenus

The study of the condensation reaction of camphoric anhydride with various aromatic compounds led us to examine initially the complete structure and stereochemistry of the ketones obtained with anisole and dimethoxy-benzene.The structure of the different