17245-30-6

Basic information

• Product Name: 3',4',5',3,5,6,7-Heptamethoxyflavone
• Synonyms: 3',4',5',3,5,6,7-Heptamethoxyflavone;3,5,6,7-TetraMethoxy-2-(3,4,5-triMethoxyphenyl)-4H-chroMen-4-one;3,5,6,7,3',4',5'-Heptamethoxyflavone
• CAS NO: 17245-30-6
• Molecular Formula: C₂₂H₂₄O₉
• Molecular Weight: 432
• Mol File: 17245-30-6.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3',4',5',3,5,6,7-Heptamethoxyflavone(CAS DataBase Reference)
• NIST Chemistry Reference: 3',4',5',3,5,6,7-Heptamethoxyflavone(17245-30-6)
• EPA Substance Registry System: 3',4',5',3,5,6,7-Heptamethoxyflavone(17245-30-6)

Safety Data

• Hazardous Substances Data: 17245-30-6(Hazardous Substances Data)

Usage

General Description

3',4',5',3,5,6,7-Heptamethoxyflavone is a chemical compound belonging to the flavone class of flavonoids. It is a natural product found in certain plants, and its structure consists of a flavone core with seven methoxy groups attached at various positions. 3',4',5',3,5,6,7-Heptamethoxyflavone has been studied for its potential biological activities, including antioxidant, anti-inflammatory, and anti-cancer properties. It has also been investigated for its potential use in the treatment of various health conditions, though more research is needed to fully understand its therapeutic potential.

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 
• 124909-81-5 6-hydroxy-3,5,7-trimethoxy-2-(3,4,5-trimethoxy-phenyl)-chromen-4-one 

Downstream Products

• 124909-91-7 Toluene-4-sulfonic acid 3,6,7-trimethoxy-4-oxo-2-(3,4,5-trimethoxy-phenyl)-4H-chromen-5-yl ester 
• 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 
• 17245-31-7 5'-hydroxy-3,6,7,3',4',5'-hexamethoxyflavone 

Relevant articles and documents

Use of flavone and flavanone derivatives in preparation of sedative and hypnotic drugs

Disclosed is a use of flavones derivatives and flavanone derivatives in preparation of sedative and hypnotic drugs.

STUDIES OF THE SELECTIVE O-ALKYLATION AND DEALKYLATION OF FLAVONOIDS. XII. A NEW, CONVENIENT METHOD FOR SYNTHESIZING 3,5-DIHYDROXY-6,7-DIMETHOXYFLAVONES FROM 3,5,6,7-TETRAMETHOXYFLAVONES

The 5-methoxy group on 3,5,6,7-tetramethoxyflavones and the 3-methoxy group on 3,6,7-trimethoxy-5-tosyloxy-flavones were selectively cleaved with anhydrous aluminum bromide in acetonitrile under controlled conditions without the cleavage of benzyloxy groups on the B ring.By the application of these reactions, seven 3,5-dihydroxy-6,7-dimethoxyflavones were easily synthesized from the corresponding 3,5,6,7-tetramethoxyflavones which were synthesized from 3,6-dihydroxy-2,4ω-trimethoxycetophenone by means of the Allan-Robinson reaction followed by methylation.Keywords: Allan-Robinson reaction ; selective demethylation; 3,5,6,7-tetramethoxyflavone; 5-hydroxy-3,6,7-trimethoxyflavone; 6-hydroxy-3,5,7-trimethoxyflavone; 5-tosyloxyflavone; 5,6-dihydroxy-3,7-dimethoxyflavone; 3,5-dihydroxy-6,7-dimethoxyflavone, 3,5-diacetoxy-6,7-dimethoxyflavone