181634-59-3

Basic information

• Product Name: 6-Bromo-2,3-dimethoxy-N-(6,7-methylenedioxy-1-naphthyl)benzamide
• Synonyms: 6-Bromo-2,3-dimethoxy-N-(6,7-methylenedioxy-1-naphthyl)benzamide
• CAS NO: 181634-59-3
• Molecular Weight: 430.255
• Mol File: 181634-59-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 6-Bromo-2,3-dimethoxy-N-(6,7-methylenedioxy-1-naphthyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Bromo-2,3-dimethoxy-N-(6,7-methylenedioxy-1-naphthyl)benzamide(181634-59-3)
• EPA Substance Registry System: 6-Bromo-2,3-dimethoxy-N-(6,7-methylenedioxy-1-naphthyl)benzamide(181634-59-3)

Safety Data

• Hazardous Substances Data: 181634-59-3(Hazardous Substances Data)

Upstream product

• 53811-49-7 naphtho[2,3-d][1,3]dioxol-5-amine 
• 60555-93-3 6-bromo-2,3-dimethoxybenzoic acid 
• 64482-27-5 2-bromo-5,6-dimethoxybenzoyl chloride 
• 56517-24-9 6,7-bis(methylsulfonyloxy)-1-nitronaphthalene 
• 77542-54-2 5-nitro-2,3-dihydroxynaphthalene 
• 142886-75-7 2,3-methylenedioxy-5-nitronaphthalene 
• 86838-09-7 ethyl (2E)-3-(2-bromo-4,5-methylenedioxyphenyl)prop-2-enoate 
• 1620902-77-3 ethyl (2E)-3-(2-allyl-4,5-methylenedioxyphenyl)prop-2-enoate 
• 1620902-84-2 (2E)-3-(2-allyl-4,5-methylenedioxyphenyl)prop-2-en-1-ol 
• 1620902-92-2 6,7-methylenedioxy-1-(2,2,2-trichloromethylcarbonylamino)-1,4-dihydronaphthalene 
• 1620902-98-8 6,7-methylenedioxy-1-(2,2,2-trichloromethylcarbonylamino)naphthalene 

Downstream Products

• 28342-33-8 oxychelerythrine 
• 181634-60-6 6-bromo-2,3-dimethoxy-N-methyl-N-(6,7-methylenedioxynaphthalen-1-yl)benzamide 

Relevant articles and documents

Synthesis of Methoxy-, Methylenedioxy-, Hydroxy-, and Halo-Substituted Benzophenanthridinone Derivatives as DNA Topoisomerase IB (TOP1) and Tyrosyl-DNA Phosphodiesterase 1 (TDP1) Inhibitors and Their Biological Activity for Drug-Resistant Cancer

As a recently discovered DNA repair enzyme, tyrosyl-DNA phosphodiesterase 1 (TDP1) removes topoisomerase IB (TOP1)-mediated DNA protein cross-links. Inhibiting TDP1 can potentiate the cytotoxicity of TOP1 inhibitors and overcome cancer cell resistance to

Total synthesis of benzo[c]phenanthridine alkaloids, chelerythrine and 12-methoxydihydrochelerythrine, by a palladium-assisted internal biaryl coupling reaction

A covenient and versatile synthesis of benzo[c]phenanthridine alkaloids, chelerythrine (1) and 12-methoxydihydrochelerythrine (5), was accomplished via an internal aryl-aryl coupling reaction of haloamides 8 and 9 by a palladium-assisted cyclization reaction.