22147-17-7

Basic information

• Product Name: Cyclohexanol, 3-phenyl-, (1R,3S)-rel-
• CAS NO: 22147-17-7
• Molecular Formula: C12H16O
• Molecular Weight: 176.258
• Mol File: 22147-17-7.mol
• Article Data: 5

Chemical Properties

• Melting Point: 82-82.5 °C(Solv: hexane (110-54-3))
• Boiling Point: 120 °C(Press: 0.9 Torr)
• Density: 1.051±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Cyclohexanol, 3-phenyl-, (1R,3S)-rel-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanol, 3-phenyl-, (1R,3S)-rel-(22147-17-7)
• EPA Substance Registry System: Cyclohexanol, 3-phenyl-, (1R,3S)-rel-(22147-17-7)

Safety Data

• Hazardous Substances Data: 22147-17-7(Hazardous Substances Data)

Upstream product

• 20795-53-3 3-phenylcyclohexanone 
• 580-51-8 [1,1'-biphenyl]-3-ol 
• 827-52-1 1-phenyl-1-cyclohexane 
• 10345-87-6 3-phenylcyclohex-2-enone 
• 108-05-4 vinyl acetate 
• 49673-74-7 3-phenyl-1-cyclohexanol 

Downstream Products

• 38383-07-2 1-bromo-3-phenyl-cyclohexane 
• 59192-35-7 4-Oxo-4-[4-(3-oxo-cyclohexyl)-phenyl]-butyric acid 

Relevant articles and documents

Aliphatic vs. aromatic C-H bond activation of phenylcyclohexane catalysed by cytochrome P450cam

Catalytic hydroxylation of phenylcyclohexane 1 by wild-type and the Y96A and Y96F mutant forms of cytochrome P450cam occurs only at the 3- and 4-positions on the cyclohexane ring, giving cis-3-phenylcyclohexanol 2, cis-4-phenylcyclohexanol 3 and trans-4-phenylcyclohexanol 4.

Lipase-mediated diastereoselective and enantioselective acetylations of 3-substituted cyclohexanols

Lipase-mediated acetylation of four diastereomeric and enantiomeric isomers of 3-substituted cyclohexanols 2 has led to an efficient resolution to provide a single stereoisomer, (1R,3S)-cyclohexyl acetate (1R,3S)-3 in a high enantiomeric excess.

Antiinflammatory phenylacetic acid derivatives. V. Phenylacetic and benzoyl-propionic acids derived from 3-phenylcyclohexanones

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