85849-24-7

Basic information

• Product Name: Cyclohexanone, 2-methyl-5-(1-methylethenyl)-3-(phenylthio)-, (2S,3R,5S)-
• CAS NO: 85849-24-7
• Molecular Formula: C16H20OS
• Molecular Weight: 260.4
• Mol File: 85849-24-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Cyclohexanone, 2-methyl-5-(1-methylethenyl)-3-(phenylthio)-, (2S,3R,5S)-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanone, 2-methyl-5-(1-methylethenyl)-3-(phenylthio)-, (2S,3R,5S)-(85849-24-7)
• EPA Substance Registry System: Cyclohexanone, 2-methyl-5-(1-methylethenyl)-3-(phenylthio)-, (2S,3R,5S)-(85849-24-7)

Safety Data

• Hazardous Substances Data: 85849-24-7(Hazardous Substances Data)

Upstream product

• 6485-40-1 (R)-Carvone 
• 108-98-5 thiophenol 

Downstream Products

• 6485-40-1 (R)-Carvone 
• 108734-55-0 (1S,2S,3R,5S)-5-isopropenyl-2-methyl-3-phenylsulfanylcyclohexanol 
• 619-01-2 dihydrocarveol 
• 5524-05-0 (2R,5R)-5-isopropenyl-2-methylcyclohexanone 
• 108734-55-0 (2S,3R,5S)-5-Isopropenyl-2-methyl-3-phenylsulfanyl-cyclohexanol 

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

The ORD, CD and UV Spectra of Sulphides Derived from Carvone

The ord and cd spectra of aromatic and aliphatic sulphides derived from carvone are compared with the spectra of dicarvone sulphide and related compounds.The spectra are discussed in relation to the structure of the molecules, as evidenced by the nmr spectrum, and correlated with the electronic transitions involved. - Keywords: Carvone sulphides; CD; NMR; ORD