7460-55-1

Basic information

• Product Name: Methyl 2-(2-broMoacetyl)benzoate
• Synonyms: Methyl 2-(2-broMoacetyl)benzoate
• CAS NO: 7460-55-1
• Molecular Formula: C₁₀H₉BrO₃
• Molecular Weight: 257.08066
• Mol File: 7460-55-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 333.4°Cat760mmHg
• Flash Point: 155.4°C
• Appearance: /
• Density: 1.494g/cm³
• Vapor Pressure: 0.000137mmHg at 25°C
• Refractive Index: 1.561
• CAS DataBase Reference: Methyl 2-(2-broMoacetyl)benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 2-(2-broMoacetyl)benzoate(7460-55-1)
• EPA Substance Registry System: Methyl 2-(2-broMoacetyl)benzoate(7460-55-1)

Safety Data

• Hazardous Substances Data: 7460-55-1(Hazardous Substances Data)

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

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

Downstream Products

• 1077-79-8 methyl 2-acetylbenzoate 
• 929613-61-6 methyl 2-(2-(3,4-difluorophenylthio)acetyl)benzoate 
• 929613-60-5 methyl 2-(2-(phenylthio)acetyl)benzoate 
• 929613-64-9 1-chloro-4-phenylthiomethylphthalazine 
• 929613-62-7 1-hydroxy-4-phenylthiomethylphthalazine 
• 929613-76-3 1-chloro-4-(3,4-difluorophenyl)thiomethylphthalazine 
• 929613-63-8 1-hydroxy-4-(3,4-difluorophenyl)thiomethylphthalazine 
• 1056632-54-2 1-(4-trifluoromethoxyanilino)-4-phenylthiomethylphthalazine 
• 929613-70-7 1-(3,5-dichloroanilino)-4-(3,4-difluorophenylthiomethyl)phthalazine 
• 929613-69-4 1-(4-fluoro-3-trifluoromethylanilino)-4-(3,4-difluorophenylthiomethyl)phthalazine 
• 1432790-77-6 C₁₈H₁₆N₄O₅S₂ 

Relevant articles and documents

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.