95782-88-0

Basic information

• Product Name: 3β-phenylcarbamoyloxy-5α-cholestane
• Synonyms: 3β-phenylcarbamoyloxy-5α-cholestane
• CAS NO: 95782-88-0
• Molecular Weight: 507.8
• Mol File: 95782-88-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3β-phenylcarbamoyloxy-5α-cholestane(CAS DataBase Reference)
• NIST Chemistry Reference: 3β-phenylcarbamoyloxy-5α-cholestane(95782-88-0)
• EPA Substance Registry System: 3β-phenylcarbamoyloxy-5α-cholestane(95782-88-0)

Safety Data

• Hazardous Substances Data: 95782-88-0(Hazardous Substances Data)

Upstream product

• 36043-80-8 chloroformiate de cholestanyle-3β 
• 80-97-7 Cholestanol 
• 103-71-9 phenyl isocyanate 
• 80-97-7 3-β-cholestanol 
• 20780-35-2 5α-cholest-14-en-3β-ol 

Downstream Products

• 84551-48-4 N-phenyl thiocarbamate de cholestanyle-3β 
• 84551-47-3 N-methyl N-phenyl carbamate de cholestanyle-3β 
• 481-21-0 cholestane 
• 80-97-7 Cholestanol 
• 35599-19-0 4-amino-benzoic acid-(5α-cholestanyl-(3β)-ester) 
• 10437-24-8 3β-formyloxy-5αH-cholestane 
• 121569-80-0 2-Amino-benzoic acid (3S,5S,8R,9S,10S,13R,14S,17R)-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester 

Relevant articles and documents

Syntheses and biological activities of a novel group of steroidal derived inhibitors for human Cdc25A protein phosphatase

Silica gel supported pyrolysis of an azido-homo-oxa steroid led to rearrangement, presumably by a mechanism similar to that of solution phase Schmidt fragmentation, to produce a group of novel inhibitors for the oncogenic cell cycle regulator Cdc25A phosp

A CONVENIENT LEWIS ACID CATALYZED PREPARATION OF CARBAMATES FROM SECONDARY ALKOHOLS AND ISOCYANATES

The Lewis acids have been found to be highly effective catalysts for the carbamate formation from secondary alcohols and isocyanates.KEYWORDS - Lewis acid; secondary alcohol; isocyanate; carbamate; γ-carbamoyloxy-α,β-enoate