473552-22-6

Basic information

• Product Name: (R)-(-)-2-azido-1-(4-benzyloxyphenyl)-1-ethanol
• Synonyms: (R)-(-)-2-azido-1-(4-benzyloxyphenyl)-1-ethanol
• CAS NO: 473552-22-6
• Molecular Weight: 269.303
• Mol File: 473552-22-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (R)-(-)-2-azido-1-(4-benzyloxyphenyl)-1-ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-(-)-2-azido-1-(4-benzyloxyphenyl)-1-ethanol(473552-22-6)
• EPA Substance Registry System: (R)-(-)-2-azido-1-(4-benzyloxyphenyl)-1-ethanol(473552-22-6)

Safety Data

• Hazardous Substances Data: 473552-22-6(Hazardous Substances Data)

Upstream product

• 831196-83-9 p-benzyloxy-ω-azidoacetophenone 
• 473552-31-7 (R)-1-(4-benzyloxyphenyl)-2-(p-tolylsulfonyloxy)ethanol 

Downstream Products

• 831196-82-8 N-[2-(4-benzyloxy-phenyl)-2-hydroxy-ethyl]-2-(3,4-dimethoxy-phenyl)-acetamide 
• 71771-90-9 denopamine 
• 63365-60-6 (R)-1-(p-benzyloxyphenyl)-2-[2-(3,4-dimethoxyphenyl)ethylamino]ethanol 
• 473552-26-0 (R)-(-)-2-amino-1-(p-benzyloxyphenyl)ethanol 
• 876-04-0 (R)-octopamine 

Relevant articles and documents

Chemoenzymatic synthesis of (R)- and (S)-tembamide, aegeline and denopamine by a one-pot lipase resolution protocol

An efficient synthesis of optically active β-azido alcohols from their ketoazides by a one-pot reduction and an in situ lipase resolution protocol is described. The synthetic utility of this procedure has been illustrated by its application in the practic

Application of optically active 1,2-diol monotosylates for synthesis of β-azido and β-amino alcohols with very high enantiomeric purity. Synthesis of enantiopure (R)-octopamine, (R)-tembamide and (R)-aegeline

A very convenient and highly efficient synthesis of near enantiopure β-azido and β-amino alcohols including biologically active substances such as (R)-octopamine, (R)-tembamide and (R)-aegeline from optically active 1,2-diol monotosylates is reported.