40088-97-9

Basic information

• Product Name: Benzenamine, N-(1,3-diphenyl-2-butenylidene)-
• CAS NO: 40088-97-9
• Molecular Formula: C22H19N
• Molecular Weight: 297.4
• Mol File: 40088-97-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzenamine, N-(1,3-diphenyl-2-butenylidene)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, N-(1,3-diphenyl-2-butenylidene)-(40088-97-9)
• EPA Substance Registry System: Benzenamine, N-(1,3-diphenyl-2-butenylidene)-(40088-97-9)

Safety Data

• Hazardous Substances Data: 40088-97-9(Hazardous Substances Data)

Upstream product

• 62-53-3 aniline 
• 98-86-2 acetophenone 
• 94-41-7 benzalacetophenone 
• 1749-19-5 N-(1-phenylethylidene)aniline 
• 1750-36-3 (E)-N-benzylidenebenzenamine 
• 1749-19-5 phenyl(1-phenylethylidene)amine 
• 925-90-6 ethylmagnesium bromide 
• 4316-37-4 1,1,-diethoxy-1-phenylethane 
• 495-45-4 dypnone 
• 142-04-1 aniline hydrochloride 

Downstream Products

• 3328-86-7 2,4-diphenylthiophene 
• 15811-37-7 1,2,4-triphenyl-1H-pyrrole 
• 612-71-5 1,3,5-triphenylbenzene 
• 62-53-3 aniline 
• 495-45-4 dypnone 

Relevant articles and documents

Efficient Thiophene Synthesis Mediated by 1,3-Bis(carboxymethyl)imidazolium Chloride: C-C and C-S Bond Formation

Thiophene derivatives have been prepared by means of a functionalized imidazolium salt [1,3-bis(carboxymethyl)imidazolium chloride] acting as a catalyst. The heterogeneous catalyst has allowed to carry out the reactions with no solvent or inert atmosphere

The potassium hydride mediated trimerization of imines

A novel reaction, the potassium hydride mediated synthesis of fulvenes, is described. The synthesis utilizes N-aryl imines as an inexpensive starting material affording novel substituted aminofulvenes. It is proposed that the presence of the metalated enamine as well as the imine (ratio 21) leads to the formation of an initial dimerization and a transient trimerization product, which cyclizes, giving rise to the aminofulvene.