167966-73-6

Basic information

• Product Name: N~1~,N~2~-dibenzyl-N'~1~,N'~2~-bis(4-methylphenyl)ethanediimidamide
• Synonyms: N~1~,N~2~-dibenzyl-N'~1~,N'~2~-bis(4-methylphenyl)ethanediimidamide
• CAS NO: 167966-73-6
• Molecular Formula: C30H30N4
• Molecular Weight: 446.586
• Mol File: 167966-73-6.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N~1~,N~2~-dibenzyl-N'~1~,N'~2~-bis(4-methylphenyl)ethanediimidamide(CAS DataBase Reference)
• NIST Chemistry Reference: N~1~,N~2~-dibenzyl-N'~1~,N'~2~-bis(4-methylphenyl)ethanediimidamide(167966-73-6)
• EPA Substance Registry System: N~1~,N~2~-dibenzyl-N'~1~,N'~2~-bis(4-methylphenyl)ethanediimidamide(167966-73-6)

Safety Data

• Hazardous Substances Data: 167966-73-6(Hazardous Substances Data)

Upstream product

• 7472-70-0 N,N'-bis(4-methylphenyl)ethanediimidoyl dichloride 
• 100-46-9 benzylamine 

Relevant articles and documents

On the Aminolysis of Bis-Imidoylchlorides of Oxalic Acid. Part I. Reaction with Aromatic and Aliphatic Amines

The reaction between bis-imidoylchlorides 2 derived from oxalic acid several aromatic and aliphatic amines was investigated.While primary aromatic amines need a thermical activation by refluxing, primary aliphatic amines give mainly at room temperature the amidines 3 in moderatly up to good yields.Proceeding from enantiomeric pure amines e.g. (R)- or (S)-1-phenylethylamine the new homochiral axalic amidines 3y and 3z with C2-symmetry were obtained.Several secondary amines react with the bis-imidoylchloride 2a to give via intramolecular cycloacylation derivatives of isatine.The new synthesized amidines 3 perform systems with a strong molecular dynamic like prototropic and E/Z-interconversion.All new compounds described were characterized by elemental analysis and spectroscopic methods.