334775-31-4

Basic information

• Product Name: (3R,1S)-(-)-3-(5-isopropylidene-1-methyl-2-oxocyclohexyl)butyric acid
• Synonyms: (3R,1S)-(-)-3-(5-isopropylidene-1-methyl-2-oxocyclohexyl)butyric acid
• CAS NO: 334775-31-4
• Molecular Weight: 238.327
• Mol File: 334775-31-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3R,1S)-(-)-3-(5-isopropylidene-1-methyl-2-oxocyclohexyl)butyric acid(CAS DataBase Reference)
• NIST Chemistry Reference: (3R,1S)-(-)-3-(5-isopropylidene-1-methyl-2-oxocyclohexyl)butyric acid(334775-31-4)
• EPA Substance Registry System: (3R,1S)-(-)-3-(5-isopropylidene-1-methyl-2-oxocyclohexyl)butyric acid(334775-31-4)

Safety Data

• Hazardous Substances Data: 334775-31-4(Hazardous Substances Data)

Upstream product

• 334775-29-0 (4R,4aS)-(-)-4,4a-dimethyl-6-isopropylidene-3,4,4a,5,6,7-hexahydroquinolin-2(1H)-one 

Downstream Products

• 15764-04-2 (4R,4aS)-(+)-4,4a-dimethyl-6-isopropylidene-4,4a,5,6,7,8-hexahydro-(3H)-naphthalen-2-one 

Relevant articles and documents

Enantioselective synthesis of (+)-α-vetivone through the Michael reaction of chiral imines

(+)-α-Vetivone has been synthesised in nine steps. The absolute stereochemistry of the two stereogenic centres is controlled in the same key step involving the stereoselective Michael addition of a chiral imine of 4-isopropylidene-2-methylcyclohexanone to phenyl crotonate.