110163-94-5

Basic information

• Product Name: Ethanone, diphenyl(phenylimino)-, (E)-
• Synonyms: .benzil N-phenyl ketoimine;1,2-Diphenyl-2-phenyliminoethanone
• CAS NO: 110163-94-5
• Molecular Formula: C20H15NO
• Molecular Weight: 285.345
• Mol File: 110163-94-5.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 441.5±28.0 °C(Predicted)
• Density: 1.05±0.1 g/cm3(Predicted)
• CAS DataBase Reference: Ethanone, diphenyl(phenylimino)-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, diphenyl(phenylimino)-, (E)-(110163-94-5)
• EPA Substance Registry System: Ethanone, diphenyl(phenylimino)-, (E)-(110163-94-5)

Safety Data

• Hazardous Substances Data: 110163-94-5(Hazardous Substances Data)

Upstream product

• 62-53-3 aniline 
• 134-81-6 benzil 
• 54212-62-3 trans-α,β-Bis-(N-methylanilino)-stilben 
• 119-53-9 2-hydroxy-2-phenylacetophenone 
• 1402072-32-5 (E)-1,2-diphenyl-2-(phenylimino)ethanol 

Downstream Products

• 93-98-1 N-phenyl benzoyl amide 
• 5722-91-8 1,2-diphenyl-2-(phenylamino)ethanone 
• 5326-56-7 N-(α'-oxo-bibenzyl-α-yl)-acetanilide 
• 80783-92-2 N-(2-Oxo-1,2-diphenyl-ethyl)-N-phenyl-propionamide 
• 102935-81-9 3-Hydroxy-2-methyl-3,4-diphenyl-4-[(E)-phenylimino]-butyric acid methyl ester 
• 104127-40-4 1,4-diphenyl-3-methoxy-3-methyl-4-benzoyl-β-azetidinone 
• 104127-40-4 1,4-diphenyl-3-methoxy-3-methyl-4-benzoyl-β-azetidinone 
• 83165-62-2 4-Benzoyl-1,3,3,4-tetraphenyl-azetidin-2-one 
• 3893-33-2 1,1',2,2'-tetraphenyl-2,2'-azinodiethanone 
• 102935-82-0 3-Hydroxy-2,2-dimethyl-3,4-diphenyl-4-[(E)-phenylimino]-butyric acid methyl ester 
• 102935-80-8 3-Hydroxy-3,4-diphenyl-4-[(E)-phenylimino]-butyric acid methyl ester 

Relevant articles and documents

Synthesis and oxidation of (E)-1,2-diphenyl-2-(arylimino) ethanol derivatives

The compounds (E)-1,2-diphenyl-2-(phenylimino)ethanol, (E)-1,2-diphenyl-2- (p-tolylimino)ethanol, and (E)-2-((4-chlorophenyl)imino)-1,2-diphenylethanol) were synthesized by reaction of a p-substituted aniline with benzoin then oxidized with chromium trioxide-triethylamine in chloroform to give (E)-1,2-diphenyl-2-(phenylimino)ethanone, (E)-1,2-diphenyl-2-(p-tolylimino) ethanone, and (E)-2-((4-chlorophenyl)imino)-1,2-diphenylethanone in very high yield. The products were characterized by IR and NMR spectral analysis.

Electrochemical Oxidation of Aromatic Enediamines. A Unique Example of Anodic Double Cyclisation to an Indolo-oxazolidine

The anodic oxidation of enediamines leads to an unexpected cyclisation involving solvent moisture to give an indolo-oxazolidine in a good yield.