7460-55-1

Usage

InChI:InChI=1/C10H9BrO3/c1-14-10(13)8-5-3-2-4-7(8)9(12)6-11/h2-5H,6H2,1H3

Upstream product

• 577-56-0 2-acetyl-benzoic acid 
• 85-44-9 phthalic anhydride 
• 1077-79-8 methyl 2-acetylbenzoate 

Downstream Products

• 929613-61-6 methyl 2-(2-(3,4-difluorophenylthio)acetyl)benzoate 
• 929613-60-5 methyl 2-(2-(phenylthio)acetyl)benzoate 
• 20863-88-1 2-ethyl-1,3,4(2H)-isoquinolinetrione 
• 21640-33-5 2-methyl-isoquinoline-1,3,4-trione 
• 21640-35-7 N-benzylisoquinoline-1,3,4(2H)-trione 

Relevant academic research and scientific papers

Capturing Intermediates in the Reaction Catalyzed by NosN, a Class C Radical S-Adenosylmethionine Methylase Involved in the Biosynthesis of the Nosiheptide Side-Ring System

Nosiheptide is a ribosomally synthesized and post-translationally modified thiopeptide natural product that possesses antibacterial, anticancer, and immunosuppressive properties. It contains a bicyclic structure composed of a large macrocycle and a unique

Capturing Intermediates in the Reaction Catalyzed by NosN, a Class C Radical S-Adenosylmethionine Methylase Involved in the Biosynthesis of the Nosiheptide Side-Ring System

Nosiheptide is a ribosomally synthesized and post-translationally modified thiopeptide natural product that possesses antibacterial, anticancer, and immunosuppressive properties. It contains a bicyclic structure composed of a large macrocycle and a unique

Synthesis and anticancer activities of novel 1,4-disubstituted phthalazines

A series of novel 1-anilino-4-(arylsulfanylmethyl)phthalazines were designed and synthesized. The structures of all the compounds were confirmed by IR, 1H-NMR, elemental analysis and MS. The analogues 1-(3-chloro-4-fluoroanilino)-4-(3,4-difluorophenylthio-methyl)phthalazine (12) and 1-(4-fluoro-3-trifluoromethylanilino)-4-(3,4-difluorophenyl-thiomethyl) phthalazine (13) showed higher activity than a cisplatin control when tested in vitro against two different cancer cell lines using the microculture tetrazolium method (MTT) method.