19795-97-2

Basic information

• Product Name: Benzenamine, N-[(4-aminophenyl)methylene]-
• CAS NO: 19795-97-2
• Molecular Formula: C13H12N2
• Molecular Weight: 196.252
• Mol File: 19795-97-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Benzenamine, N-[(4-aminophenyl)methylene]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, N-[(4-aminophenyl)methylene]-(19795-97-2)
• EPA Substance Registry System: Benzenamine, N-[(4-aminophenyl)methylene]-(19795-97-2)

Safety Data

• Hazardous Substances Data: 19795-97-2(Hazardous Substances Data)

Upstream product

• 556-18-3 4-aminobenzaldehyde 
• 7732-18-5 water 
• 142-04-1 aniline hydrochloride 
• 62-53-3 aniline 
• 64-17-5 ethanol 
• 6421-26-7 bis-[4-(phenylimino-methyl)-phenyl]-diazene-N-oxide 
• 10359-18-9 N-(4-nitrobenzyl)aniline 
• 623-04-1 4-aminobenzenemethanol 
• 1227476-15-4 Azobenzene 
• 785-80-8 p-nitrobenzylideneaniline 

Downstream Products

• 81286-07-9 4-amino-3,5-dinitro-benzaldehyde 

Relevant articles and documents

Synthetic method of imine

The invention relates to a method for preparing imine from an azo compound and an alcohol compound through hydrogen transition coupling. The method specifically comprises: dispersing and dissolving an azo compound and an alcohol compound which are taken as substrates in an organic solvent, adding a nickel-based catalyst, putting the obtained mixture in a synthesis kettle, leading inert gas in to replace internal air, performing sealing and stirring, carrying out a heating reaction, performing centrifugation to remove the catalyst after the reaction is over, performing rotary evaporation to remove the solvent, and performing purification through recrystallization to obtain the sample. In the catalytic action of different multi-phase nickel-based catalysts, the reaction is high in conversion rate and imine selectivity. The method is an atom economic reaction.