168749-08-4

Basic information

• Product Name: (1R,2S)-cis-2-azidocyclohexanol
• Synonyms: (1R,2S)-cis-2-azidocyclohexanol
• CAS NO: 168749-08-4
• Molecular Weight: 141.173
• Mol File: 168749-08-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (1R,2S)-cis-2-azidocyclohexanol(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2S)-cis-2-azidocyclohexanol(168749-08-4)
• EPA Substance Registry System: (1R,2S)-cis-2-azidocyclohexanol(168749-08-4)

Safety Data

• Hazardous Substances Data: 168749-08-4(Hazardous Substances Data)

Upstream product

• 108-05-4 vinyl acetate 
• 286-20-4 cyclohexane-1,2-epoxide 
• 110-83-8 cyclohexene 
• 924654-89-7 (S)-Hydroxy-phenyl-acetic acid (1R,2R)-2-bromo-cyclohexyl ester 
• 924654-97-7 2-bromocyclohexyl 2-oxo-2-phenylacetate 
• 924654-99-9 Oxo-phenyl-acetic acid (1R,2S)-2-azido-cyclohexyl ester 
• 260260-98-8 Acetic acid (1R,2S)-2-azido-cyclohexyl ester 

Downstream Products

• 260065-86-9 (1R,2S)-2-amino-1-cyclohexanol 

Relevant articles and documents

Single enantiomer epoxides by bromomandelation of prochiral alkenes

A combination of mandelic acid and N-bromosuccinimide efficiently converts prochiral alkenes into a readily separable 1:1 mixture of the bromomandelates. The diastereomerically pure bromomandelates are then converted into a variety of enantiomerically pure products. Terminal alkenes are converted into enantiomerically pure epoxides. Cyclohexene is converted into enantiomerically pure cis-2-azidocyclohexanol and cis-2-phenylthiocyclohexanol.