131965-52-1

Basic information

• Product Name: (S)-(+)-2-bromo-1-(4-benzyloxyphenyl)ethanol
• Synonyms: (S)-(+)-2-bromo-1-(4-benzyloxyphenyl)ethanol
• CAS NO: 131965-52-1
• Molecular Weight: 307.187
• Mol File: 131965-52-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (S)-(+)-2-bromo-1-(4-benzyloxyphenyl)ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-(+)-2-bromo-1-(4-benzyloxyphenyl)ethanol(131965-52-1)
• EPA Substance Registry System: (S)-(+)-2-bromo-1-(4-benzyloxyphenyl)ethanol(131965-52-1)

Safety Data

• Hazardous Substances Data: 131965-52-1(Hazardous Substances Data)

Upstream product

• 4254-67-5 2-bromo-1-(4-benzyloxyphenyl)-1-ethanone 

Downstream Products

• 72734-74-8 (p-benzyloxy-phenyl)-ethyleneoxide 

Relevant articles and documents

Microbial reduction of ω-bromoacetophenones in the presence of surfactants

Several ω-bromoacetophenone derivatives 6a-f were reduced to (R)-(-)-2-bromo-1-(phenyl/substituted phenyl) ethanol derivatives 7a-f with whole cell biocatalysts in good yields. The enantiomeric excesses were increased to 95% using an anionic surfactant under an inert atmosphere in an aqueous medium. Copyright (C) 2000 Elsevier Science Ltd.

A convenient stereoselective synthesis of (R)-(-)-denopamine and (R)-(-)-salmeterol

β-Adrenoreceptor agonists (R)-(-)-denopamine (R)-1 and (R)-(-)-salmeterol (R)-2 have been prepared in good overall yield and high enantioselectivity through a biotransformative pathway.