71918-53-1

Basic information

• Product Name: (+)-N,N'-Dimethyl-N,N'-bis<(R)-1-phenylethyl>-1,2-ethylendiamin
• Synonyms: (+)-N,N'-Dimethyl-N,N'-bis<(R)-1-phenylethyl>-1,2-ethylendiamin
• CAS NO: 71918-53-1
• Molecular Weight: 296.456
• Mol File: 71918-53-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (+)-N,N'-Dimethyl-N,N'-bis<(R)-1-phenylethyl>-1,2-ethylendiamin(CAS DataBase Reference)
• NIST Chemistry Reference: (+)-N,N'-Dimethyl-N,N'-bis<(R)-1-phenylethyl>-1,2-ethylendiamin(71918-53-1)
• EPA Substance Registry System: (+)-N,N'-Dimethyl-N,N'-bis<(R)-1-phenylethyl>-1,2-ethylendiamin(71918-53-1)

Safety Data

• Hazardous Substances Data: 71918-53-1(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 76740-22-2 (+)-N,N'-Bis<(R)-1-phenylethyl>-1,2-ethylendiamin 
• 5933-40-4 (R)-(+)-N,α-dimethylbenzylamine 
• 106-93-4 ethylene dibromide 

Relevant articles and documents

Studies on the Occurrence of Hydrogen Transfer, 73. - The Reduction of Prochiral Alkyl (Aryl) Ketones with Alkali Metal Amalgams Forming Carbinols and Pinakols

The factors are determined which influence the stereochemistry and the ratio (C/P) in the reduction of acetophenone with lithium, sodium, and potassium amalgam (Li/Hg, Na/Hg, K/Hg) leading to carbinol (C) and pinacol(P).The C/P ratio is influenced a) by proton donators, b) by quaternaryammonium salts, c) by bis-tertiary amines.In the presence of optically active quaternary ammonium salts and optically active bis-tertiary amines a low optical induction is observed both in pinacol and carbinol.An anomal dimerization product 20 is formed in the reduction of pivalophenone with Li/Hg.