871835-37-9

Basic information

• Product Name: ethyl [2-(2-bromobenzoyl)-4-methylphenoxy]acetate
• Synonyms: ethyl [2-(2-bromobenzoyl)-4-methylphenoxy]acetate
• CAS NO: 871835-37-9
• Molecular Weight: 377.235
• Mol File: 871835-37-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: ethyl [2-(2-bromobenzoyl)-4-methylphenoxy]acetate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl [2-(2-bromobenzoyl)-4-methylphenoxy]acetate(871835-37-9)
• EPA Substance Registry System: ethyl [2-(2-bromobenzoyl)-4-methylphenoxy]acetate(871835-37-9)

Safety Data

• Hazardous Substances Data: 871835-37-9(Hazardous Substances Data)

Upstream product

• 55270-73-0 (2-bromophenyl)(2-hydroxy-5-methylphenyl)methanone 
• 105-39-5 chloroacetic acid ethyl ester 

Downstream Products

• 1630042-88-4 2 [2 (2 bromobenzoyl) 4 methylphenoxy]methyl-1,3,4 oxadiazole 
• 1578261-61-6 ethyl (N'-{2-[2-(2-bromobenzoyl)-4-methylphenoxy]acetyl}hydrazinocarbonyl)acetate 
• 848439-45-2 2-[2-(2-bromobenzoyl)-4-methylphenoxy]acetohydrazide 
• 871835-39-1 [2-(2-bromo-benzoyl)-4-methyl-phenoxy]-acetic acid 

Relevant articles and documents

Synthesis and tumor inhibitory activity of novel coumarin analogs targeting angiogenesis and apoptosis

A sequence of coumarin analogs 5a-j was obtained by multi step synthesis from hydroxy benzophenones (1a-j). The in vitro antiproliferative effect of the title compounds was tested against Ehrlich ascites carcinoma (EAC) and Daltons lymphoma ascites (DLA)

Anti-tumor and proapoptotic effect of novel synthetic benzophenone analogues in Ehrlich ascites tumor cells

A series of substituted benzophenone analogues, (2-aroyl-4-methylphenoxy) acetamides 4a-e, have been synthesized via three-step synthesis sequence beginning with the 2-hydroxybenzophenones 1a-e in excellent yield. 1a-e on reaction with ethyl chloroacetate