160332-20-7

Basic information

• Product Name: (-)-(1R,2S)-1-phenyl-2-chloro-1-propanol
• Synonyms: (-)-(1R,2S)-1-phenyl-2-chloro-1-propanol
• CAS NO: 160332-20-7
• Molecular Weight: 170.639
• Mol File: 160332-20-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (-)-(1R,2S)-1-phenyl-2-chloro-1-propanol(CAS DataBase Reference)
• NIST Chemistry Reference: (-)-(1R,2S)-1-phenyl-2-chloro-1-propanol(160332-20-7)
• EPA Substance Registry System: (-)-(1R,2S)-1-phenyl-2-chloro-1-propanol(160332-20-7)

Safety Data

• Hazardous Substances Data: 160332-20-7(Hazardous Substances Data)

Upstream product

• 6084-17-9 2-chloro-1-phenylpropan-1-one 
• 93-55-0 1-phenyl-propan-1-one 
• 766-90-5 cis-1-phenyl-1-propylene 
• 873-66-5 1-propenylbenzene 

Downstream Products

• 14212-54-5 (+)-(R,R)-β-methylstyrene oxide 

Relevant articles and documents

Method for preparing chiral (1R,2S)-1-phenyl-2-(1-pyrrolidyl)propane-1-alcohol

The invention provides a new method for simply and feasibly synthesizing (1R,2S)-1-phenyl-2-(1-pyrrolidyl)propane-1-alcohol through enzymatic catalysis. The method is easy to operate and mild in condition, an intermediate does not need to be separated, th

Chemoenzymatic synthesis of chiral epoxides. Preparation of 4-phenyl-2,3- epoxybutane and 1-phenyl-1,2-epoxypropane

All the stereoisomers of 4-phenyl-2,3-epoxybutane and 1-phenyl-1,2- epoxypropane (β-methylstyrene oxide) have been prepared in three steps from 4-phenyl-2-butanone and 1-phenyl-2-propanone or 1-phenyl-1-propanone respectively. The key step is the microbiological reduction of the corresponding haloketones. These results confirm those previously described and demonstrate that the chemoenzymatic synthesis of homochiral 2,3-epoxides is a general method that can be used whatever the starting ketone.