65957-22-4

Basic information

• Product Name: N¹-methyl-N¹,N²-diphenylacetamidine
• Synonyms: N¹-methyl-N¹,N²-diphenylacetamidine
• CAS NO: 65957-22-4
• Molecular Weight: 224.305
• Mol File: 65957-22-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N¹-methyl-N¹,N²-diphenylacetamidine(CAS DataBase Reference)
• NIST Chemistry Reference: N¹-methyl-N¹,N²-diphenylacetamidine(65957-22-4)
• EPA Substance Registry System: N¹-methyl-N¹,N²-diphenylacetamidine(65957-22-4)

Safety Data

• Hazardous Substances Data: 65957-22-4(Hazardous Substances Data)

Upstream product

• 10341-75-0 (E)-1-phenylethanone oxime 
• 100-61-8 N-methylaniline 
• 19433-17-1 acetophenone O-acetyloxime 
• 33567-67-8 N-Methyl-N-<(trimethylsilyl)ethinyl>anilin 
• 65957-03-1 N,N'-dimethyl-N,N'-diphenylethene-1,1-diamine 
• 103-84-4 Acetanilid 

Relevant articles and documents

Access to Amidines and Arylbenzimidazoles: Zinc-Promoted Rearrangement of Oxime Acetates

An efficient and straightforward zinc-promoted rearrangement of oxime acetates with arylamines for the synthesis of amidines has been developed under mild conditions. This process involves N?O/C?C bond cleavages and C?C/C?N bond formations. Various oxime

Facile one-pot syntheses of amidines and enamines from oximes via Beckmann rearrangement using trifluoromethanesulfonic anhydride

Iminocarbocation intermediates were in situ-generated by treating various oximes with trifluoromethanesulfonic anhydride (Tf2O) in the presence of triethylamine in toluene and nucleophilic trapping with amines or sodium enolates under mild conditions afforded the corresponding amidines and enamines. Some of the thus-obtained enamines were converted to 2-substituted 4-oxo-3-quinolinecarboxylic acid derivatives by subsequent intramolecular Friedel-Crafts acylation.