773899-62-0

Basic information

• Product Name: 6-Chloro-2-((E)-styryl)-chromen-4-one
• Synonyms: 6-Chloro-2-((E)-styryl)-chromen-4-one
• CAS NO: 773899-62-0
• Molecular Weight: 282.726
• Mol File: 773899-62-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 6-Chloro-2-((E)-styryl)-chromen-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Chloro-2-((E)-styryl)-chromen-4-one(773899-62-0)
• EPA Substance Registry System: 6-Chloro-2-((E)-styryl)-chromen-4-one(773899-62-0)

Safety Data

• Hazardous Substances Data: 773899-62-0(Hazardous Substances Data)

Upstream product

• 386212-36-8 1-(5-chloro-2-hydroxy-phenyl)-5-phenyl-penta-2,4-dien-1-one 
• 663190-87-2 6-chloro-3-methoxy-2-styryl-chromen-4-one 
• 69693-00-1 6-chloro-2-methyl-4H-chromen-4-one 
• 100-52-7 benzaldehyde 

Downstream Products

• 133405-93-3 9-chloro-4-phenyl-3a,4,11a,11b-tetrahydro-2,6-dioxa-cyclopenta[a]anthracene-1,3,11-trione 
• 133405-97-7 9-chloro-2,4-diphenyl-3a,4,11a,11b-tetrahydro-chromeno[3,2-e]isoindole-1,3,11-trione 
• 133406-21-0 6-chloro-2-(1,2-dibromo-2-phenyl-ethyl)-chromen-4-one 

Relevant articles and documents

Studies on unimolecular and bimolecular photoprocesses of a newly synthesized selenium compound, 7-chloro-2-phenyl-9H-[1]-benzopyrano[3,2-b]-selenophene-9-one (SeP)

Using steady state/time resolved spectroscopic and electrochemical techniques the spectroscopic and photophysical studies were made on a novel synthesized selenophene compound SeP in nonpolar methylcyclohexane (MCH), polar aprotic acetonitrile (ACN) and p

SOME REACTIONS OF 6-CHLORO-2-METHYL-4H-1-BENZOPYRAN-4-ONE. I

4H-1-Benzopyran-4-ones (Chromones) are proved to be of special importance in medicine as stimulants of the central nervous system, spasmolytics, coronary dilators, inhibitors for the growth of human cancer cells, reductants for blood pressure, diuretics, antiallergic, antibiotics and cardiovascular agents. In the course of the present work several new derivatives containing the chromone moiety were prepared. Some of their reactions were investigated in the hope of obtaining new compounds having biological activities. The reactivities of chromone nucleus towards cycloaddition reactions under Diels-Alder conditions, nucleophilic and electrophilic reagents, photocyclodehydrogenation and thiation have been investigated.