1170682-16-2

Basic information

• Product Name: (1R,2R,3S,4R)-2-(4-bromophenyl)-3-cyano-4-hydroxy-3-(methoxycarbonyl)cyclohexanecarboxylic acid
• Synonyms: (1R,2R,3S,4R)-2-(4-bromophenyl)-3-cyano-4-hydroxy-3-(methoxycarbonyl)cyclohexanecarboxylic acid
• CAS NO: 1170682-16-2
• Molecular Weight: 382.211
• Mol File: 1170682-16-2.mol

Chemical Properties

• CAS DataBase Reference: (1R,2R,3S,4R)-2-(4-bromophenyl)-3-cyano-4-hydroxy-3-(methoxycarbonyl)cyclohexanecarboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2R,3S,4R)-2-(4-bromophenyl)-3-cyano-4-hydroxy-3-(methoxycarbonyl)cyclohexanecarboxylic acid(1170682-16-2)
• EPA Substance Registry System: (1R,2R,3S,4R)-2-(4-bromophenyl)-3-cyano-4-hydroxy-3-(methoxycarbonyl)cyclohexanecarboxylic acid(1170682-16-2)

Safety Data

• Hazardous Substances Data: 1170682-16-2(Hazardous Substances Data)

Upstream product

• 1170682-08-2 (1S,2R,3R,6R)-methyl 2-(4-bromophenyl)-1-cyano-3-formyl-6-hydroxycyclohexanecarboxylate 

Relevant articles and documents

Organocatalytic enantioselective domino synthesis of highly functionalized cyclohexanes with an all-carbon quaternary stereocenter

A highly enantioselective organocatalytic domino Michael/aldol reaction is presented. The reaction is catalyzed by chiral amines and gives access to highly functionalized cyclohexanes with one all-carbon quaternary stereocenter and multiple chiral stereoc