1640-44-4

Basic information

• Product Name: Benzamide, N-(2-acetylphenyl)-4-chloro-
• CAS NO: 1640-44-4
• Molecular Formula: C15H12ClNO2
• Molecular Weight: 273.719
• Mol File: 1640-44-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzamide, N-(2-acetylphenyl)-4-chloro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N-(2-acetylphenyl)-4-chloro-(1640-44-4)
• EPA Substance Registry System: Benzamide, N-(2-acetylphenyl)-4-chloro-(1640-44-4)

Safety Data

• Hazardous Substances Data: 1640-44-4(Hazardous Substances Data)

Upstream product

• 79498-43-4 2-(4-Chloro-phenyl)-3-methyl-3H-indol-3-yl-hydroperoxide 
• 2142-69-0 2-bromophenyl methyl ketone 
• 619-56-7 4-chlorobenzamide 
• 551-93-9 2-aminoacetophenone 
• 122-01-0 4-chloro-benzoyl chloride 

Downstream Products

• 1643-59-0 2-(4-chlorophenyl)-4-methylquinazoline 3-oxide 
• 1640-50-2 N-(p-Chlorbenzoyl)-2-aminoacetophenonoxim 
• 106657-37-8 N-methyl-2-(p-chlorophenyl)-quinolin-4(1H)-one 
• 78396-10-8 2-(4’-chlorophenyl)-4-quinolone 

Relevant articles and documents

E-N-(2-acetyl-phenyl)-3-phenyl-acrylamide targets abrin and ricin toxicity: Hitting two toxins with one stone

The efficacy of small molecule inhibitors (SMIs) against the enzymatic activity of Shiga toxin prompted the evaluation of their efficacy on related toxins viz. ricin and abrin. Ricin, like Shiga toxin, is listed as a category B bioweapon and belongs to th

Copper-mediated selective C-H activation and cross-dehydrogenative C-N coupling of 2′-aminoacetophenones

Isatins were obtained by cross-dehydrogenative C-N annulation and dealkylative C-N annulation of 2′-N-aryl/alkylaminoacetophenones and 2′-N,N-dialkylaminoacetophenones respectively in the presence of Cu(OAc)2·H2O/NaOAc/air. However, on reaction with CuBr, 2′-N-benzylaminoacetophenones underwent selective oxidation of an α-methylene group of amine rather than the 2-acetyl group to provide corresponding benzamides exclusively. Base played an important role in selective oxidation by lowering the temperature and time.

THE REARRANGEMENT OF HYDROPEROXYINDOLENINES

Examination of a series of substituted 3-(hydroxyperoxy)indolenines favours a mechanism for base catalysed decomposition of the dioxetan rather than Criegee type.