1032315-50-6

Basic information

• Product Name: dibenzyl 2-(2'-selenophenyl)-6,7-methylenedioxyquinolin-4-yl-phosphate
• Synonyms: dibenzyl 2-(2'-selenophenyl)-6,7-methylenedioxyquinolin-4-yl-phosphate
• CAS NO: 1032315-50-6
• Molecular Weight: 578.42
• Mol File: 1032315-50-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: dibenzyl 2-(2'-selenophenyl)-6,7-methylenedioxyquinolin-4-yl-phosphate(CAS DataBase Reference)
• NIST Chemistry Reference: dibenzyl 2-(2'-selenophenyl)-6,7-methylenedioxyquinolin-4-yl-phosphate(1032315-50-6)
• EPA Substance Registry System: dibenzyl 2-(2'-selenophenyl)-6,7-methylenedioxyquinolin-4-yl-phosphate(1032315-50-6)

Safety Data

• Hazardous Substances Data: 1032315-50-6(Hazardous Substances Data)

Upstream product

• 22968-45-2 Selenophene-2-carboxylic acid 
• 39082-07-0 selenophene-2-carbonyl chloride 
• 1032315-85-7 6,7-methylenedioxy-2-(selenophen-2-yl)quinolin-4(1H)-one 
• 990-91-0 dibenzyl [[bis(benzyloxy)phosphoryl]oxy]phosphonate 

Relevant articles and documents

NOVEL HYDROPHILIC DERIVATIVES OF 2-ARYL-4-QUINOLONES AS ANTICANCER AGENTS

2-aryl-4-quinolones are converted into phosphates by reacting with tetrabenzyl pyrophosphate to form dibenzyl phosphates thereof, which are then subject to hydrogenation to replace dibenzyl groups with H, followed by reacting with Amberlite IR-120(Na+ form) to form disodium salts. The results of preliminary screening revealed that these phosphates showed significant anti-cancer activity. A novel intermediate, 2-selenophene 4-quinolone and Λ/, Λ/-dialkylaminoalkyl derivatives of 2-phenyl-4-quinolones are also synthesized. These novel intermediates exhibited significant anticancer activities.