758691-53-1

Basic information

• Product Name: (1R,2R)-N,N'-dibenzoyl-1,2-bis(2-methoxyphenyl)-1,2-ethanediamine
• Synonyms: (1R,2R)-N,N'-dibenzoyl-1,2-bis(2-methoxyphenyl)-1,2-ethanediamine
• CAS NO: 758691-53-1
• Molecular Weight: 480.563
• Mol File: 758691-53-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (1R,2R)-N,N'-dibenzoyl-1,2-bis(2-methoxyphenyl)-1,2-ethanediamine(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2R)-N,N'-dibenzoyl-1,2-bis(2-methoxyphenyl)-1,2-ethanediamine(758691-53-1)
• EPA Substance Registry System: (1R,2R)-N,N'-dibenzoyl-1,2-bis(2-methoxyphenyl)-1,2-ethanediamine(758691-53-1)

Safety Data

• Hazardous Substances Data: 758691-53-1(Hazardous Substances Data)

Upstream product

• 100-44-7 benzyl chloride 
• 758691-50-8 (1R,2R)-1,2-bis(2-methoxyphenyl)-1,2-ethanediamine 
• 578-57-4 2-bromoanisole 
• 758691-47-3 (1R,2R)-1,2-bis(2-methoxyphenyl)-N,N'-bis[(S)-1-phenylethyl]-1,2-ethanediamine 
• 58520-46-0 N,N'-(1,2-bis(2-methoxyphenyl)ethane-1,2-diyl)dibenzamide 
• 98-88-4 benzoyl chloride 

Relevant articles and documents

Enantioselective Reductive Coupling of Imines Templated by Chiral Diboron

We herein report a general, practical, and highly efficient method for asymmetric synthesis of a wide range of chiral vicinal diamines via reductive coupling of imines templated by chiral diboron. The protocol features high enantioselectivity and stereospecificity, mild reaction conditions, simple operating procedures, use of readily available starting materials, and a broad substrate scope. The method signifies the generality of diboron-enabled [3,3]-sigmatropic rearrangement.