1534-15-2

Basic information

• Product Name: Benzenamine, N-[3-(dimethylamino)-2-propenylidene]-
• CAS NO: 1534-15-2
• Molecular Formula: C11H14N2
• Molecular Weight: 174.246
• Mol File: 1534-15-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Benzenamine, N-[3-(dimethylamino)-2-propenylidene]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, N-[3-(dimethylamino)-2-propenylidene]-(1534-15-2)
• EPA Substance Registry System: Benzenamine, N-[3-(dimethylamino)-2-propenylidene]-(1534-15-2)

Safety Data

• Hazardous Substances Data: 1534-15-2(Hazardous Substances Data)

Upstream product

• 67250-03-7 1,1-dimethyl-5-phenyl-1H-1,5-diazapentadienium perchlorate 
• 1611-79-6 1-Anilino-3-dimethylimonio-propen-⁽¹⁾-methylsulfat 
• 62-53-3 aniline 
• 927-63-9 3-dimethylaminoacrolein 

Downstream Products

• 63114-19-2 1-(3-Dimethylamino-propyl)-1,3-diphenyl-urea 
• 96-54-8 N-Methylpyrrole 
• 91-22-5 quinoline 
• 62-53-3 aniline 
• 86129-94-4 N,3,3-Triphenyl-4-(dimethylamino)-3,4-dihydro-2-pyridone 
• 13658-95-2 N¹,N¹-dimethyl-N³-phenylpropane-1,3-diamine 

Relevant articles and documents

Thermolysis of Polyazapentadienes. Part 8. The formation of Pyrroles from 1,1-Dialkyl-5-aryl-1,5-diazapentadienes

Flash vacuum pyrolysis of the 1,5-diazapentadienes (4)-(10) gave moderate yields of pyrroles together with quinolines, formed by electrocyclic ring closure with elimination.The pyrroles were formed by hydrogen transfer from an N-alkyl group, followed by cyclisation and final aromatisation of the resulting dihydropyrrole intermediate by free-radical cleavage.The mechanism of the hydrogen transfer and cyclisation is not known with certainty, but may involve diradicals or 1,5-dipolar intermediates.