128316-23-4

Basic information

• Product Name: 2-benzhydryl-3-oxo-N,3-diphenylpropanamide
• Synonyms: 2-benzhydryl-3-oxo-N,3-diphenylpropanamide
• CAS NO: 128316-23-4
• Molecular Weight: 405.496
• Mol File: 128316-23-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-benzhydryl-3-oxo-N,3-diphenylpropanamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-benzhydryl-3-oxo-N,3-diphenylpropanamide(128316-23-4)
• EPA Substance Registry System: 2-benzhydryl-3-oxo-N,3-diphenylpropanamide(128316-23-4)

Safety Data

• Hazardous Substances Data: 128316-23-4(Hazardous Substances Data)

Upstream product

• 118081-87-1 N-phenyl-β-diphenylmethylbenzoylpyruvamide 
• 50395-70-5 N,N-diphenylcinnamamide 
• 119-53-9 2-hydroxy-2-phenylacetophenone 
• 102-92-1 cinnamoyl chloride 
• 621-82-9 Cinnamic acid 
• 101-81-5 Diphenylmethane 
• 959-66-0 3-oxo-3-phenylpropionanilide 

Relevant articles and documents

UV light-mediated difunctionalization of alkenes through aroyl radical addition/1,4-/1,2-Aryl shift cascade reactions

UV light-mediated difunctionalization of alkenes through an aroyl radical addition/1,4-/1,2-aryl shift has been described. The resulted aroyl radical from a photocleavage reaction added to acrylamide compounds followed by cyclization led to the formation of oxindoles, whereas the addition to cinnamic amides aroused a unique 1,4-aryl shift reaction. Furthermore, the difunctionalization of alkenes of prop-2-en-1-ols was also achieved through aroyl radical addition and a sequential 1,2-aryl shift cascade reaction.

CHEMISTRY OF OXALYL DERIVATIVES OF METHYL KETONES XLVII. REACTION OF N-ARYLAROYLPYRUVAMIDES WITH DIPHENYLDIAZOMETHANE

N-Aryl-4-aryl-3-diphenylmethyl-2,4-dioxobutyramides were obtained from N-arylaroylpyruvamides and diphenyldiazomethane.At 110 deg C in toluene they were converted into N-aryl-3-aryl-2-diphenylmethyl-3-oxopropionamides.By boiling in acetic acid they were converted into 1,5-diaryl-4-diphenylmethyl-2,3-dihydro-2,3-pyrrolediones.