82801-37-4

Usage

InChI:InChI=1/C17H22O4/c1-16(2)13(9-10-17(16,3)15(19)20)14(18)11-5-7-12(21-4)8-6-11/h5-8,13H,9-10H2,1-4H3,(H,19,20)/t13-,17+/m0/s1

Upstream product

• 100-66-3 methoxybenzene 
• 76-32-4 (±)-camphoric acid anhydride 
• 57078-08-7 acide cis-p-anisoyl-3 trimethyl-1,2,2 cyclopentane carboxylique 
• 595-31-3 (+)-(1S,3R)-1,2,2-trimethylcyclopentane-1,3-dicarboxylic anhydride 
• 145415-55-0 acide (-)-cis-p-anisoyl-3 trimethyl-1,2,2 cyclopentane carboxylique 
• 93764-46-6 chlorure de l'acide (-)-cis-p-anisoyl-3 trimethyl-1,2,2 cyclopentane carboxylique 

Downstream Products

• 93740-32-0 ester methylique de l'acide (-)-trans-p-anisoyl-3 trimethyl-1,2,2 cyclopentane carboxylique 
• 93740-32-0 ester methylique de l'acide (-)-cis-p-anisoyl-3 trimethyl-1,2,2 cyclopentane carboxylique 

Relevant academic research and scientific papers

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

3-(4'-Alkoxy-benzoyl)-1,2,2-trimethylcyclopentane-carboxylic acids, methods of use and compositions containing such compounds

The invention relates to 3-(4'-alkoxy-benzoyl)-1,2,2-trimethyl-cyclopentane-carboxylic acids, and to their optical isomers; they are useful as active principles for anorexigenic drugs.