3443-28-5

Basic information

• Product Name: 3,5,7-Trihydroxy-4',8-dimethoxyflavone
• Synonyms: 3,5,7-Trihydroxy-4',8-dimethoxyflavone;3,5,7-Trihydroxy-8-methoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one;Prudomestin;3,5,7-Trihydroxy-8,4'-dimethoxyflavone;Herbacetin 8,4'-dimethyl ether
• CAS NO: 3443-28-5
• Molecular Formula: C₁₇H₁₄O₇
• Molecular Weight: 330.2889
• Mol File: 3443-28-5.mol
• Article Data: 1

Chemical Properties

• Melting Point: 209-210 °C
• Boiling Point: 568.855 °C at 760 mmHg
• Flash Point: 212.199 °C
• Appearance: /
• Density: 1.507 g/cm³
• PKA: 6.65±0.40(Predicted)
• CAS DataBase Reference: 3,5,7-Trihydroxy-4',8-dimethoxyflavone(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5,7-Trihydroxy-4',8-dimethoxyflavone(3443-28-5)
• EPA Substance Registry System: 3,5,7-Trihydroxy-4',8-dimethoxyflavone(3443-28-5)

Safety Data

• Hazardous Substances Data: 3443-28-5(Hazardous Substances Data)

Usage

General Description

3,5,7-Trihydroxy-4',8-dimethoxyflavone is a naturally occurring chemical compound found in various plants, including fruits and vegetables. It is classified as a flavonoid, which is a type of plant-based compound known for its antioxidant properties and potential health benefits. 3,5,7-Trihydroxy-4',8-dimethoxyflavone is known to possess anti-inflammatory and anti-cancer properties and has been studied for its potential to inhibit the growth of cancer cells. Additionally, it has been found to have potential neuroprotective effects and may help in the prevention of neurodegenerative diseases. 3,5,7-Trihydroxy-4',8-dimethoxyflavone has also shown promise in improving cardiovascular health and supporting overall immune function. Further research is needed to fully understand the potential health benefits and uses of 3,5,7-Trihydroxy-4',8-dimethoxyflavone.

Upstream product

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• 117155-43-8 5-hydroxy-4',8-dimethoxy-3,7-bis(tosyloxy)flavone 

Relevant articles and documents

Studies of the selective O-alkylation and dealkylation of flavonoids. XI. A new convenient method for synthesizing 3,5,7-trihydroxy-8-methoxyflavones from 7-hydroxy-3,5,8-trimethoxyflavones

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