13567-79-8

Basic information

• Product Name: (-)-(4aR,7R)-4,4a,5,6,7,8-hexahydro-7-isopropenyl-4a-methylnaphthalene-2(3H)-one
• Synonyms: (-)-(4aR,7R)-4,4a,5,6,7,8-hexahydro-7-isopropenyl-4a-methylnaphthalene-2(3H)-one
• CAS NO: 13567-79-8
• Molecular Weight: 204.312
• Mol File: 13567-79-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (-)-(4aR,7R)-4,4a,5,6,7,8-hexahydro-7-isopropenyl-4a-methylnaphthalene-2(3H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: (-)-(4aR,7R)-4,4a,5,6,7,8-hexahydro-7-isopropenyl-4a-methylnaphthalene-2(3H)-one(13567-79-8)
• EPA Substance Registry System: (-)-(4aR,7R)-4,4a,5,6,7,8-hexahydro-7-isopropenyl-4a-methylnaphthalene-2(3H)-one(13567-79-8)

Safety Data

• Hazardous Substances Data: 13567-79-8(Hazardous Substances Data)

Upstream product

• 6485-40-1 (R)-Carvone 
• 13567-75-4 (4aR,7R,8aR)-8a-hydroxy-7-isopropenyl-4a-methyloctahydro-2(1H)-naphthalenone 
• 6322-49-2 4-chloro-2-butanone 
• 5524-05-0 (2R,5R)-5-isopropenyl-2-methylcyclohexanone 

Relevant articles and documents

An Improved Synthesis of Homochiral Octalones from (-)-Carvone

A novel diastereoselective route to octalones 3 and 4 has been developed.The key step involves an asymmetric Michael addition of the corresponding chiral imine, derived from R-(+)-dihydrocarvone, to methyl vinyl ketone.

The Synthesis and X-Ray Structure of a New Eudesmane Sesquiterpene Alcohol, 4-hydroxy-10-epi-eudesm-11-ene

-