72923-08-1

Basic information

• Product Name: Benzenemethanamine, a-(2-imino-2-phenylethylidene)-N-(4-methylphenyl)-
• CAS NO: 72923-08-1
• Molecular Formula: C22H20N2
• Molecular Weight: 312.414
• Mol File: 72923-08-1.mol

Chemical Properties

• CAS DataBase Reference: Benzenemethanamine, a-(2-imino-2-phenylethylidene)-N-(4-methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanamine, a-(2-imino-2-phenylethylidene)-N-(4-methylphenyl)-(72923-08-1)
• EPA Substance Registry System: Benzenemethanamine, a-(2-imino-2-phenylethylidene)-N-(4-methylphenyl)-(72923-08-1)

Safety Data

• Hazardous Substances Data: 72923-08-1(Hazardous Substances Data)

Upstream product

• 72923-17-2 4,6-diphenyl-1-p-tolylpyrimidin-2(1H)-one 
• 4209-15-8 N-(1-phenyl-ethylidene)-p-toluidine 
• 100-47-0 benzonitrile 

Downstream Products

• 1083-30-3 dihydrochalcone 
• 106-49-0 p-toluidine 
• 96355-37-2 3,5-Diphenyl-2H-1,2-thiazin-1,1-dioxid 
• 1859-00-3 N-(4-methylphenyl)benzamidine 
• 2648-61-5 2,2-dichloroacetophenone 
• 106291-90-1 (1R,3R)-1,3-Diphenyl-N,N'-di-p-tolyl-propane-1,3-diamine 
• 106291-99-0 (1R,3S)-1,3-Diphenyl-N,N'-di-p-tolyl-propane-1,3-diamine 
• 106292-08-4 (4R,6R)-4,6-Diphenyl-1,3-di-p-tolyl-tetrahydro-pyrimidin-2-one 
• 4571-27-1 2-chloro-1,3-diphenyl-propane-1,3-dione 
• 88039-29-6 4-bromo-3,5-diphenyl-2-(p-tolyl)-1,2,6-thiadiazine S-oxide 
• 88039-42-3 5-bromo-1,2-dihydro-2-oxo-4,6-diphenyl-1-p-tolylpyrimidine 
• 88039-39-8 5-Chloro-4,6-diphenyl-1-p-tolyl-1H-pyrimidin-2-one 
• 88039-35-4 4-Bromo-3,5-diphenyl-1-p-tolyl-1H-pyrazole 
• 88039-32-1 4-Chloro-3,5-diphenyl-1-p-tolyl-1H-pyrazole 

Relevant articles and documents

New Synthesis of 4-amino-1-Azadienes by Addition of Zn-Enolates to Nitriles

A synthesis of 4-amino-1-azadienes 1 by addition of Zn-enolates of Schiff bases to nitriles is described.This method improves the yields achieved by the former one using AlCl3.Key words: Synthesis; 4-amino-1-azadienes; Zn-enolates.

Novel Synthesis of Di-imines by the Transformation of 1-Aryl-4,6-disubstituted Pyrimidin-2(1H)-ones

The di-imines (4), which are versatile starting materials for the synthesis of heterocycles, are obtained in fair yields when the 1-aryl-4,6-disubstituted pyrimidin-2(1H)-ones (3) are treated with alkoxide, both photochemically and thermally.The di-imines (4) thus obtained, when treated with disulphide, give the 1,3-thiazine-2-thiones (8) and/or the 1-arylpyrimidine-2(1H)-thiones (9).