857682-06-5

Basic information

• Product Name: (1R,6S)-6-benzoyl-cyclohex-3-enecarboxylic acid
• Synonyms: (1R,6S)-6-benzoyl-cyclohex-3-enecarboxylic acid
• CAS NO: 857682-06-5
• Molecular Weight: 230.263
• Mol File: 857682-06-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (1R,6S)-6-benzoyl-cyclohex-3-enecarboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,6S)-6-benzoyl-cyclohex-3-enecarboxylic acid(857682-06-5)
• EPA Substance Registry System: (1R,6S)-6-benzoyl-cyclohex-3-enecarboxylic acid(857682-06-5)

Safety Data

• Hazardous Substances Data: 857682-06-5(Hazardous Substances Data)

Upstream product

• 935-79-5 cis-1,2,3,6-tetrahydrophthalic anhydride 
• 31211-31-1 racemic cis-6-benzoylcyclohex-3-enecarboxylic acid 
• 857682-05-4 (1R,6S)-6-benzoyl-1-[(4S)-4-isopropyl-1,3-thiazolidine-2-thion-3-yl]carbonylcyclohex-3-ene 
• 1078-58-6 diphenylzinc 

Relevant articles and documents

Selective substituent transfer from mixed zinc reagents in Ni-catalyzed anhydride alkylation

(Chemical Equation Presented) The use of mixed zinc reagents in Ni-catalyzed anhydride alkylation results in preferential transfer of substituents (Ph > Me > Et ? iPr ～ TMSCH2) for the ligands bipy, dppe, and iPrPHOX. Utilization of such mixed

A palladium-catalyzed enantioselective alkylative desymmetrization of meso-succinic anhydrides

Monoalkylation of cyclic anhydrides provides an opportunity to couple a carbon-carbon bond-forming event with the control of backbone stereochemistry. We have developed a palladium-JOSIPHOS catalyst system that desymmetrizes meso-succinic anhydrides using organozinc reagents as nucleophiles, and have found that, in many cases, this reaction proceeds at ambient temperature. Copyright