882303-12-0

Basic information

• Product Name: 2-(3,4-dimethoxyphenyl)-3-phenyl-9H-xanthen-9-one
• Synonyms: 2-(3,4-dimethoxyphenyl)-3-phenyl-9H-xanthen-9-one
• CAS NO: 882303-12-0
• Molecular Weight: 408.453
• Mol File: 882303-12-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-(3,4-dimethoxyphenyl)-3-phenyl-9H-xanthen-9-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3,4-dimethoxyphenyl)-3-phenyl-9H-xanthen-9-one(882303-12-0)
• EPA Substance Registry System: 2-(3,4-dimethoxyphenyl)-3-phenyl-9H-xanthen-9-one(882303-12-0)

Safety Data

• Hazardous Substances Data: 882303-12-0(Hazardous Substances Data)

Upstream product

• 6380-23-0 3,4-dimethoxystyrene 
• 752233-11-7 (E)-3-bromo-2-(2-phenylvinyl)-4H-chromen-4-one 
• 16636-62-7 1-(2'-hydroxyphenyl)butane-1,3-dione 
• 1172141-18-2 (E,E)-3-[2-(3,4-dimethoxyphenyl)vinyl]-2-(2-phenylvinyl)-4H-chromen-4-one 
• 104387-28-2 3-bromo-2-styrylchromone 
• 118-93-4 o-hydroxyacetophenone 
• 7250-94-4 o-acetoxyacetophenone 
• 69932-31-6 3-bromo-2-methyl-4H-chromen-4-one 

Downstream Products

• 1011792-17-8 2-(3,4-dihydroxyphenyl)-3-phenyl-9H-xanthen-9-one 

Relevant articles and documents

2,3-Diarylxanthones as strong scavengers of reactive oxygen and nitrogen species: A structure-activity relationship study

Xanthones are a class of oxygen-containing heterocyclic compounds widely distributed in nature. The natural derivatives can present different substitutions in the xanthone core that include hydroxyl, methoxyl, prenyl and glycosyl groups. The inclusion of

A novel and efficient route for the synthesis of hydroxylated 2,3-diarylxanthones

A novel, efficient and general route for the synthesis of hydroxylated 2,3-diarylxanthones is described. 3-Bromo-2-styryl-chromone, the key intermediate of this synthesis, is obtained by a Baker-Venkataraman rearrangement of the appropriate 2′-cinnamoylox