924660-44-6

Basic information

• Product Name: 2-bromo-5-methoxy-N-phenylbenzamide
• Synonyms: 2-bromo-5-methoxy-N-phenylbenzamide
• CAS NO: 924660-44-6
• Molecular Weight: 306.159
• Mol File: 924660-44-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-bromo-5-methoxy-N-phenylbenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromo-5-methoxy-N-phenylbenzamide(924660-44-6)
• EPA Substance Registry System: 2-bromo-5-methoxy-N-phenylbenzamide(924660-44-6)

Safety Data

• Hazardous Substances Data: 924660-44-6(Hazardous Substances Data)

Upstream product

• 56658-04-9 2-bromo-5-methoxybenzoyl chloride 
• 62-53-3 aniline 
• 22921-68-2 2-bromo-5-methoxy-benzoic acid 

Downstream Products

• 38088-95-8 8-methoxyphenanthridine-6(5H)-one 
• 1610724-85-0 2-bromo-N-(4-phenyl)-N-(methoxymethyl)-5-methoxybenzamide 
• 1357830-08-0 6-methoxy-3-phenylquinazolin-4(3H)-one 

Relevant articles and documents

Synthesis of 5-methyl phenanthridium derivatives: A new class of human DOPA decarboxylase inhibitors

DOPA decarboxylase (DDC) is responsible for the decarboxylation of l-DOPA and related aromatic amino acids and correlates closely with a number of clinical disorders. Sanguinarine, a natural quaternary benzophenanthridine alkaloid (QBA), was reported to b

Efficient synthesis of phenanthridinone derivatives via a palladium-catalyzed coupling process

(Chemical Equation Presented) A palladium-mediated domino reaction was developed to conveniently synthesize phenanthridinone derivatives. Phosphine ligand 1 strongly promotes the domino process, which includes aryl-aryl coupling and C-N bond formations concomitant with a deamidation reaction. The versatility and applicability to a broad range of substrates make this reaction useful for the development of bioactive derivatives.