17245-31-7

Basic information

• Product Name: 4H-1-Benzopyran-4-one, 5-hydroxy-3,6,7-trimethoxy-2-(3,4,5-trimethoxyphenyl)-
• CAS NO: 17245-31-7
• Molecular Formula: C21H22O9
• Molecular Weight: 418.4
• Mol File: 17245-31-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4H-1-Benzopyran-4-one, 5-hydroxy-3,6,7-trimethoxy-2-(3,4,5-trimethoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 4H-1-Benzopyran-4-one, 5-hydroxy-3,6,7-trimethoxy-2-(3,4,5-trimethoxyphenyl)-(17245-31-7)
• EPA Substance Registry System: 4H-1-Benzopyran-4-one, 5-hydroxy-3,6,7-trimethoxy-2-(3,4,5-trimethoxyphenyl)-(17245-31-7)

Safety Data

• Hazardous Substances Data: 17245-31-7(Hazardous Substances Data)

Upstream product

• 30250-35-2 5,7-dihydroxy-3,3',4',5',6-pentamethoxyflavone 
• 77-78-1 dimethyl sulfate 
• 14639-73-7 1-(3,6-dihydroxy-2,4-dimethoxy-phenyl)-2-methoxy-ethanone 
• 1719-88-6 3,4,5-trimethoxybenzoic anhydride 
• 17245-30-6 3,5,6,7,3',4',5'-hepta methoxyl-flavone 

Downstream Products

• 17245-32-8 5-O-acetyl-3,6,7,3’,4’,5’-hexa-O-methylflavone 
• 124909-98-4 Toluene-4-sulfonic acid 3-hydroxy-6,7-dimethoxy-4-oxo-2-(3,4,5-trimethoxy-phenyl)-4H-chromen-5-yl ester 
• 124910-07-2 Acetic acid 3-acetoxy-6,7-dimethoxy-4-oxo-2-(3,4,5-trimethoxy-phenyl)-4H-chromen-5-yl ester 
• 72357-39-2 3,5-Dihydroxy-6,7-dimethoxy-2-(3,4,5-trimethoxy-phenyl)-chromen-4-one 
• 124909-91-7 Toluene-4-sulfonic acid 3,6,7-trimethoxy-4-oxo-2-(3,4,5-trimethoxy-phenyl)-4H-chromen-5-yl ester 

Relevant articles and documents

Antivascular and anti-parasite activities of natural and hemisynthetic flavonoids from New Caledonian Gardenia species (Rubiaceae)

A series of 16 flavonoids were isolated and prepared from bud exudate of Gardenia urvillei and Gardenia oudiepe, endemic to New Caledonia. Most of them are rare polymethoxylated flavones. Some of these compounds showed noticeable activity against Leishmania (Leishmania) amazonensis, Plasmodium falciparum and Trypanosoma brucei gambiense, in addition to tubulin polymerization inhibition at low micromolar concentration. We also provide a full set of NMR data as some of the flavones were incompletely described.