23112-19-8

Basic information

• Product Name: Benzamide, N-(3-oxo-1,3-diphenyl-1-propenyl)-, (Z)-
• CAS NO: 23112-19-8
• Molecular Formula: C22H17NO2
• Molecular Weight: 327.382
• Mol File: 23112-19-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzamide, N-(3-oxo-1,3-diphenyl-1-propenyl)-, (Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N-(3-oxo-1,3-diphenyl-1-propenyl)-, (Z)-(23112-19-8)
• EPA Substance Registry System: Benzamide, N-(3-oxo-1,3-diphenyl-1-propenyl)-, (Z)-(23112-19-8)

Safety Data

• Hazardous Substances Data: 23112-19-8(Hazardous Substances Data)

Upstream product

• 95932-17-5 -1 phenyl-5 tetrazole 
• 98815-39-5 (Z)-3-amino-1,3-diphenylprop-2-en-1-one 
• 98-88-4 benzoyl chloride 
• 120-46-7 1,3-diphenylpropanedione 

Downstream Products

• 1174154-30-3 (R,E)-N-(1,3-diphenylallyl)benzamide 
• 1176888-02-0 (S)-2,4,6-triphenyl-4H-1,3-oxazine 
• 1289142-69-3 (S,E)-N-(1,3-diphenylallyl)benzamide 
• 91875-49-9 (S)-N-(3-oxo-1,3-diphenylpropyl)benzamide 
• 91875-49-9 (R)-N-(3-oxo-1,3-diphenylpropyl)benzamide 
• 3274-61-1 2,4,5-triphenylpyrrole 

Relevant articles and documents

Asymmetric synthesis of 4H-1,3-oxazines: Enantioselective reductive cyclization of N-acylated β-amino enones with trichlorosilane catalyzed by chiral Lewis bases

N-Acylated β-amino enones reductively cyclize by treatment with trichlorosilane and a chiral Lewis base catalyst to afford optically active 4H-1,3-oxazines, which can be transformed to other chiral compounds without racemization.

Reactivite du nucleophile azoture vis-a-vis de cations heterocycliques aromatiques. VIII. Rearrangement de β-tetrazolo-trans-benzalacetophenones

β-Tetrazolyl-trans-benzalacetophenones (T) isomerize upon heating into the corresponding azido-azomethines (A).These non-isolable products undergo various transformations depending on the reaction conditions.With organic bases such as triphenylphosphine or pyridine, their interception can occur.In aromatic solvents, a rearrangement involving loss of nitrogen leads to five-membered diazoted heterocycles: N-benzoyl imidazoles and pyrazoles, via intermediate diazirines and oxazepines.Protic solvents have been found to facilitate the isomerisation of tetrazoles into azidoazomethines.Solvolysis of the azidooxazine and in some cases of the oxazinium species resulting from the equilibrium and reaction: are then observed.