1134564-21-8

Basic information

• Product Name: (2R,1'R)-N-benzyl-N-(2'-methoxy-1'-phenylethyl)-2-bromo-3-methylbutylamine
• Synonyms: (2R,1'R)-N-benzyl-N-(2'-methoxy-1'-phenylethyl)-2-bromo-3-methylbutylamine
• CAS NO: 1134564-21-8
• Molecular Weight: 390.363
• Mol File: 1134564-21-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (2R,1'R)-N-benzyl-N-(2'-methoxy-1'-phenylethyl)-2-bromo-3-methylbutylamine(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,1'R)-N-benzyl-N-(2'-methoxy-1'-phenylethyl)-2-bromo-3-methylbutylamine(1134564-21-8)
• EPA Substance Registry System: (2R,1'R)-N-benzyl-N-(2'-methoxy-1'-phenylethyl)-2-bromo-3-methylbutylamine(1134564-21-8)

Safety Data

• Hazardous Substances Data: 1134564-21-8(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 514168-48-0 (S)-2-Isopropyl-1-((R)-2-methoxy-1-phenyl-ethyl)-aziridine 

Downstream Products

• 1134564-30-9 (2R,1'R)-1-[N-benzyl-N-(2'-methoxy-1'-phenylethyl)amino]-3-methylbutan-2-ol 

Relevant articles and documents

Substituent effects in regio- And stereoselective ring-opening reaction of aziridines with ET3N·3HF for β-fluoroamine synthesis

This paper discusses the reactivity of various 2-substituted aziridine derivatives. The reaction of chiral 2-aryl-substituted aziridines with triethylamine trihydrofluoride (Et3N·3HF) afforded chiral E-fluoroamines with high stereoselectivity. In contrast