51145-18-7

Basic information

• Product Name: N-(2-benzoyl-4-chlorophenyl)-N-methylnitrous amide
• Synonyms: N-(2-benzoyl-4-chlorophenyl)-N-methylnitrous amide
• CAS NO: 51145-18-7
• Molecular Weight: 274.707
• Mol File: 51145-18-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-(2-benzoyl-4-chlorophenyl)-N-methylnitrous amide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-benzoyl-4-chlorophenyl)-N-methylnitrous amide(51145-18-7)
• EPA Substance Registry System: N-(2-benzoyl-4-chlorophenyl)-N-methylnitrous amide(51145-18-7)

Safety Data

• Hazardous Substances Data: 51145-18-7(Hazardous Substances Data)

Upstream product

• 932-96-7 N-methyl(p-chloroaniline) 
• 611-73-4 Benzoylformic acid 
• 98-86-2 acetophenone 
• 1007-19-8 4-chloro-N-methyl-N-nitrosoaniline 

Downstream Products

• 51145-19-8 5-chloro-1-nitroso-3-phenylindolin-3-ol 
• 439-14-5 diazepam 

Relevant articles and documents

Palladium-catalyzed decarboxylative ortho-acylation of N-nitrosoanilines with α-oxocarboxylic acids

A palladium-catalyzed efficient C-H acylation reaction of N-nitrosoanilines with α-oxocarboxylic acids has been developed. The reaction proceeded smoothly with potassium persulfate as the oxidant to afford acylated N-nitrosoanilines in moderate to good yi

Palladium-catalyzed ortho-acylation of N-Nitrosoanilines with α-oxocarboxylic acids: A convenient method to synthesize N-Nitroso ketones and indazoles

An efficient and mild protocol for regioselective synthesis of N-Nitroso aryl ketones by palladium-catalyzed direct acylation of arenes using N-Nitroso as directing groups is described. This reaction proceeded smoothly and could tolerate a variety of functional groups. Moreover, this chemistry offers a convenient access to a range of indazoles.

A new synthesis of indoles

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