863482-65-9

Basic information

• Product Name: 1-((R)-2-azidopropyl)benzene
• Synonyms: 1-((R)-2-azidopropyl)benzene
• CAS NO: 863482-65-9
• Molecular Weight: 161.206
• Mol File: 863482-65-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-((R)-2-azidopropyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-((R)-2-azidopropyl)benzene(863482-65-9)
• EPA Substance Registry System: 1-((R)-2-azidopropyl)benzene(863482-65-9)

Safety Data

• Hazardous Substances Data: 863482-65-9(Hazardous Substances Data)

Upstream product

• 122-78-1 phenylacetaldehyde 
• 4436-24-2 1,2-epoxy-3-phenylpropane 
• 103-79-7 1-phenyl-acetone 
• 608130-32-1 (R)-3-phenyl-2-(N-phenylaminooxy)propan-1-ol 
• 155498-78-5 Toluene-4-sulfonic acid (R)-2-hydroxy-3-phenyl-propyl ester 
• 17131-14-5 (R)-3-phenylpropane-1,2-diol 
• 61393-94-0 (R)-2-benzyloxirane 
• 1517-68-6 (S)-1-phenylpropan-2-ol 
• 104-53-0 3-phenyl-propionaldehyde 
• 53334-59-1 (S)-1-phenylpropan-2-yl 4-methylbenzenesulfonate 

Downstream Products

• 167421-83-2 tert-butyl N-[(1R)-1-methyl-2-phenylethyl]carbamate 
• 33817-09-3 (R)-2-methylamino-1-phenylpropane 
• 2323-36-6 SELEGILINE 
• 156-34-3 l-amphetamine 

Relevant articles and documents

Synthesis of (R)-selegiline via hydrolytic kinetic resolution

A short and enantioselective formal synthesis of (R)-selegiline has been achieved using Jacobsen's hydrolytic kinetic resolution (HKR) of phenyl propylene oxide.

Asymmetric syntheses of both enantiomers of amphetamine hydrochloride via bakers' yeast reduction of phenylacetone

Both enantiomers of amphetamine hydrochloride were stereospecifically synthesised based on bakers' yeast reduction of phenylacetone. A simple and efficient method for the chiral inversion of (S)-1-phenyl-2-propanol 3 to (R)-1-phenyl-2-propanol 8 has been discussed.