108734-55-0

Basic information

• Product Name: (1S,2S,3R,5S)-5-isopropenyl-2-methyl-3-phenylsulfanylcyclohexanol
• Synonyms: (1S,2S,3R,5S)-5-isopropenyl-2-methyl-3-phenylsulfanylcyclohexanol
• CAS NO: 108734-55-0
• Molecular Weight: 262.416
• Mol File: 108734-55-0.mol

Chemical Properties

• CAS DataBase Reference: (1S,2S,3R,5S)-5-isopropenyl-2-methyl-3-phenylsulfanylcyclohexanol(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S,3R,5S)-5-isopropenyl-2-methyl-3-phenylsulfanylcyclohexanol(108734-55-0)
• EPA Substance Registry System: (1S,2S,3R,5S)-5-isopropenyl-2-methyl-3-phenylsulfanylcyclohexanol(108734-55-0)

Safety Data

• Hazardous Substances Data: 108734-55-0(Hazardous Substances Data)

Upstream product

• 85849-24-7 (2S,3R,5S)-5-isopropenyl-2-methyl-3-phenylsulfanylcyclohexanone 
• 108-98-5 thiophenol 

Downstream Products

• 1252794-64-1 (1S,2S,2''R,3R,5S)-2-(4-isobutylphenyl)propionic acid 5-isopropenyl-2-methyl-3-phenylsulfanylcyclohex-1-yl ester 
• 5524-05-0 (2R,5R)-5-isopropenyl-2-methylcyclohexanone 
• 619-01-2 dihydrocarveol 

Relevant articles and documents

Chiral auxiliary-mediated enantioenrichment of (±)-ibuprofen, under steglich conditions, with secondary alcohols derived from (R)-carvone

The synthesis of a series of chiral secondary alcohols derived from (R)-carvone, and the stereochemical outcome of their reaction with (±)-ibuprofen, is reported. The racemic drug was transformed into the corresponding diastereomeric esters mediated by DC

Stereospecific synthesis of (+) 2R, 5R trans dihydrocarvone from (-) carvone

(+) 2R, 5R trans dihydrocarvone was prepared stereospecifically in a large scale experiment by stereospecific addition of thiophenol to the conjugated double bond of (-) carvone, followed by desulfurization.