807643-22-7

Upstream product

• 807643-19-2 ethyl [2-(4-methylbenzoyl)-4-methylphenoxy]acetate 
• 26880-95-5 (4-methylphenyl)(2-hydroxy-5-methylphenyl)methanone 

Downstream Products

• 871037-25-1 [5-methyl-2-(5-thioxo-4,5-dihydro-[1,3,4]oxadiazol-2-ylmethoxy)-phenyl]-p-tolyl-methanone 
• 1578261-68-3 ethyl (N'-{2-[2-(4-methylbenzoyl)-4-methylphenoxy]acetyl}hydrazinocarbonyl)acetate 
• 1630042-92-0 2-[2(4-methylbenzoyl)-4-methylphenoxy]methyl-1,3,4-oxadiazole 
• 871037-30-8 [2-(4-amino-5-thioxo-4,5-dihydro-1H-[1,2,4]triazol-3-ylmethoxy)-5-methyl-phenyl]-p-tolyl-methanone 

Relevant academic research and scientific papers

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)

Synthesis and evaluation of in vitro antimicrobial activity of novel 2-[2-(aroyl)aroyloxy]methyl-1,3,4-oxadiazoles

Synthetic pathway of the ten novel 2-[2-(aroyl)aroyloxy]methyl-1,3,4- oxadiazoles as new potential antimicrobial agents is illustrated. Intramolecular cyclization of 2-(2-aroylaryloxy) aceto hydrazides to 2-[2-(aroyl)aroyloxy] methyl-1,3,4-oxadiazoles was

Synthesis and antimicrobial study of novel heterocyclic compounds from hydroxybenzophenones

The triazolothiadiazine analogues 6a-e were obtained via a multistep synthesis sequences beginning with the hydroxybenzophenones 1a-e. Hydroxybenzophenones on reaction with ethyl chloroacetate affords ethyl (2-aroylaryloxy)acetates 2a-e which on treatment