6944-19-0

Basic information

• Product Name: Propanimidamide,N,N'-diphenyl-
• Synonyms: Propionamidine,N,N'-diphenyl- (6CI,7CI); N,N'-Diphenylpropionamidine; NSC 53884
• CAS NO: 6944-19-0
• Molecular Formula: C15H16 N2
• Molecular Weight: 224.305
• Mol File: 6944-19-0.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 375.3°Cat760mmHg
• Flash Point: 180.8°C
• Density: 0.99g/cm³
• CAS DataBase Reference: Propanimidamide,N,N'-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Propanimidamide,N,N'-diphenyl-(6944-19-0)
• EPA Substance Registry System: Propanimidamide,N,N'-diphenyl-(6944-19-0)

Safety Data

• Hazardous Substances Data: 6944-19-0(Hazardous Substances Data)

Upstream product

• 13879-93-1 methylketene diethyldithioacetal 
• 62-53-3 aniline 
• 7719-09-7 thionyl chloride 
• 60-29-7 diethyl ether 
• 2157-50-8 propiophenone oxime 
• 133145-92-3 1-phenylpropan-1-one O-acetyl oxime 

Downstream Products

• 146361-81-1 chlorobis(N,N'-diphenylpropionamidinato)(triphenylphosphine)ruthenium(III) 
• 146344-65-2 dichlorobis(N,N'-diphenylpropionamidinato)osmium(IV) 
• 142496-68-2 carbonyl(N,N'-diphenylpropioamidinato)hydridobis(triphenylphosphine)osmium(II) 
• 363610-02-0 bis(N,N'-diphenylpropionamidinato)norbornadieneruthenium(II) 
• 97870-30-9 2-ethyl-1-phenyl-1H-benzo[d]imidazole 
• 142496-76-2 Os(CF₃COO)(C₆H₅NC(C₂H₅)NC₆H₅)(CO)(P(C₆H₅)3)2 
• 142496-79-5 Ru(C₆H₅NC(C₂H₅)NC₆H₅)2(CO)(P(C₆H₅)3) 
• 152375-84-3 carbonyl(N,N'-diphenylpropioamidinato)trifluoroacetatobis(triphenylphosphine)ruthenium(II) 
• 143202-22-6 IrH₂(C₆H₅NC(C₂H₅)NC₆H₅)(P(C₆H₅)3)2 
• 143202-22-6 (N,N'-diphenylpropioamidinato)dihydridobis(triphenylphosphine)iridium(III) 
• 142496-53-5 RuH(C₆H₅NC(C₂H₅)NC₆H₅)(CO)(P(C₆H₅)3)2 
• 142496-53-5 carbonyl(N,N'-diphenylpropioamidinato)hydridobis(triphenylphosphine)ruthenium(II) 
• 152441-24-2 carbonylchloro(N,N'-diphenylpropioamidinato)bis(triphenylphosphine)osmium(II) 
• 142496-47-7 RuCl(C₆H₅NC(C₂H₅)NC₆H₅)(CO)(P(C₆H₅)3)2 

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