52190-13-3

Basic information

• Product Name: N-benzyl-2-bromo-N-phenylacetamide
• Synonyms: N-benzyl-2-bromo-N-phenylacetamide
• CAS NO: 52190-13-3
• Molecular Weight: 304.186
• Mol File: 52190-13-3.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: N-benzyl-2-bromo-N-phenylacetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-2-bromo-N-phenylacetamide(52190-13-3)
• EPA Substance Registry System: N-benzyl-2-bromo-N-phenylacetamide(52190-13-3)

Safety Data

• Hazardous Substances Data: 52190-13-3(Hazardous Substances Data)

Upstream product

• 758640-21-0 N-Benzylaniline 
• 598-21-0 2-Bromoacetyl bromide 
• 22118-09-8 2-bromoacetyl chloride 

Downstream Products

• 112482-71-0 N-benzyl-2-diazo-N-phenylacetamide 
• 1217-89-6 1-benzylisatin 
• 847437-08-5 diethyl (1-benzyl-2-oxoindolin-3-yl)phosphonate 
• 119288-67-4 diethyl (+/-)-trans-1,4-diphenyl-2-oxo-azetidin-3-yl-phosphonate 
• 847437-06-3 [(benzyl-phenyl-carbamoyl)-diazo-methyl]-phosphonic acid diethyl ester 
• 779335-37-4 [(benzyl-phenyl-carbamoyl)-methyl]-phosphonic acid diethyl ester 
• 86096-75-5 2,2'-<1,8-Naphthalindiylbis(4,1-phenylenoxy)>bis 
• 86096-74-4 2,2'-<1,8-Naphthalinbis(oxy)>bis 

Relevant articles and documents

Electrochemical dehydrogenative cyclization of 1,3-dicarbonyl compounds

The intramolecular C(sp3)-H/C(sp2)-H cross-coupling of 1,3-dicarbonyl compounds has been achieved through Cp2Fe-catalyzed electrochemical oxidation. The key to the success of these dehydrogenative cyclization reactions is

A copper(II)-mediated radical cross-dehydrogenative coupling/sulfinic acid elimination approach to 2-quinolones

A new cyclisation procedure to prepare 4-carboxy-quinolin-2-ones via a one-pot Cu(II)-mediated radical cross-dehydrogenative coupling/sulfinic acid elimination of linear anilides is described. Extensions to more complex substrates are also reported as are

Transition-Metal-Free Fluoroarylation of Diazoacetamides: A Complementary Approach to 3-Fluorooxindoles

An efficient transition-metal-free fluoroarylation reaction of N-aryl diazoacetamides with NFSI (N-fluorobenzenesulfonimide) is described. This reaction directly provides 3-fluorooxindole derivatives in yields of 67-93% with high selectivity via a carbene