5554-37-0

Basic information

• Product Name: benzilanilide
• Synonyms: benzilanilide
• CAS NO: 5554-37-0
• Molecular Weight: 303.36
• Mol File: 5554-37-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: benzilanilide(CAS DataBase Reference)
• NIST Chemistry Reference: benzilanilide(5554-37-0)
• EPA Substance Registry System: benzilanilide(5554-37-0)

Safety Data

• Hazardous Substances Data: 5554-37-0(Hazardous Substances Data)

Upstream product

• 62-53-3 aniline 
• 52182-15-7 ethyl benzilate 
• 119-61-9 benzophenone 
• 103-71-9 phenyl isocyanate 
• 4695-14-1 2,2-diphenylacetanilide 
• 525-06-4 diphenyl ketene 
• 2902-98-9 2-chloro-2,2-diphenylacetyl chloride 
• 861523-34-4 bromo-diphenyl-acetic acid anilide 
• 7647-01-0 hydrogenchloride 
• 22278-19-9 ethoxy-diphenyl-acetic acid anilide 
• 741-36-6 1,1-diphenyl-1-chloroacetanilide 
• 7732-18-5 water 
• 298230-73-6 anilino-diphenyl-acetic acid anilide 
• 22050-98-2 methoxy-diphenyl-acetic acid anilide 

Downstream Products

• 22278-19-9 ethoxy-diphenyl-acetic acid anilide 
• 22050-98-2 methoxy-diphenyl-acetic acid anilide 
• 1922-79-8 3,3-diphenyl-1,3-dihydro-indol-2-one 
• 41007-80-1 benzilic acid-(4-bromo-anilide) 
• 741-36-6 1,1-diphenyl-1-chloroacetanilide 
• 117-34-0 2,2-diphenylacetic acid 
• 4695-14-1 2,2-diphenylacetanilide 
• 63483-15-8 5-bromo-3,3-diphenyl-indolin-2-one 

Relevant articles and documents

A kind of α-hydroxy amides the synthetic method of the compound of

The invention provides a method for synthesizing an alpha-hydroxy amide compound. The method specifically comprises the following steps: (1) mixing amide, an alkali and dimethyl sulfoxide, sealing in an air atmosphere, and reacting; (2) cooling to room te

Nucleophilic Addition of Lanthanoid Metal Umpoled Diaryl Ketones to Electrophiles

Ytterbium metal promoted cross-coupling reactions of diaryl ketones with a variety of electrophiles are described.Diaryl ketones treated with 1-2 equiv of Yb metal react smoothly with other ketones, nitriles, epoxides, CO2, etc., to give the corresponding unsymmetrical pinacols, α-hydroxy ketones, 1,3-diols, α-hydroxy carboxylic acids, etc., in good yields respectively.These reactions occur via nucleophilic addition of the intermediates 4a-c to electrophiles.Reaction of benzophenone (1a) with Yb metal is discussed in detail and some information on the composition of the intermediates of the reaction of diaryl ketones with Yb metal are also given.