74881-61-1

Basic information

• Product Name: 2-bromo-N-methyl-N-(2-naphthyl)benzamide
• CAS NO: 74881-61-1
• Molecular Weight: 340.219
• Mol File: 74881-61-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-bromo-N-methyl-N-(2-naphthyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromo-N-methyl-N-(2-naphthyl)benzamide(74881-61-1)
• EPA Substance Registry System: 2-bromo-N-methyl-N-(2-naphthyl)benzamide(74881-61-1)

Safety Data

• Hazardous Substances Data: 74881-61-1(Hazardous Substances Data)

Upstream product

• 571165-08-7 2-Bromo-N-naphthalen-2-yl-benzamide 
• 77-78-1 dimethyl sulfate 
• 7154-66-7 2-bromobenzoic acid chloride 
• 91-59-8 naphthalen-2-ylamine 

Downstream Products

• 35118-21-9 N-methylbenzenophenanthridinone 
• 2216-67-3 2-N-methylaminonaphthalene 
• 74881-63-3 N-methyl-2-(naphthalen-2-yl)benzamide 

Relevant articles and documents

Electrochemical Reactions. Part 23. Intramolecular Radical Substitution during the Reduction of 2-Halogeno-N-methyl-N-naphthylbenzamides

Phenyl radical intermediates formed by the reductive cleavage of the carbon-halogen bond in 2-halogeno-N-methyl-N-(1-naphthyl)benzamides undergo intramolecular substitution to give N-methyl-2-(1-naphthyl)benzamide, and no N-methylbenzophenanthridone is formed.Reduction of 2-halogeno-N-methyl-N-(2-naphthyl)benzamides gives N-methyl-2-(2-naphthyl)benzamide, N-methylbenzophenanthridone, and N-methylbenzophenanthridone.These results complete our comparison of this electrochemical reaction with related radical Pschorr cyclisations.Further reduction of these initial reaction products occurs that only qualitative conclusions can be drawn from the product yields.