65548-55-2

Basic information

• Product Name: 3',4',7,8-TETRAMETHOXYFLAVONE
• Synonyms: TETRAMETHOXYFLAVONE, 3',4',7,8-;7,8,3',4'-TETRAMETHOXYFLAVONE;3',4',7,8-TETRAMETHOXYFLAVONE;TETRAMETHOXYFLAVONE, 3',4',7,8-(RG);2-(3,4-Dimethoxyphenyl)-7,8-dimethoxy-4H-chromen-4-one
• CAS NO: 65548-55-2
• Molecular Formula: C₁₉H₁₈O₆
• Molecular Weight: 342.34
• Product Categories: Tetra-substituted Flavones
• Mol File: 65548-55-2.mol
• Article Data: 5

Chemical Properties

• Melting Point: 206-208°C
• Appearance: /
• BRN: 330821
• CAS DataBase Reference: 3',4',7,8-TETRAMETHOXYFLAVONE(CAS DataBase Reference)
• NIST Chemistry Reference: 3',4',7,8-TETRAMETHOXYFLAVONE(65548-55-2)
• EPA Substance Registry System: 3',4',7,8-TETRAMETHOXYFLAVONE(65548-55-2)

Safety Data

• Hazard Codes: T
• Statements: 25
• Safety Statements: 22-24/25-45
• Hazardous Substances Data: 65548-55-2(Hazardous Substances Data)

Usage

General Description

3',4',7,8-Tetramethoxyflavone is a type of chemical compound that belongs to the family of Flavones, which are essentially aromatically unsaturated organic compounds. It's a specific kind of flavonoid, which are compounds known for their diverse and beneficial health effects due to their antioxidant properties. There is limited specific information about this compound, it's not common and widely studied as other flavonoids. Flavonoids like 3',4',7,8-Tetramethoxyflavone are typically found in a variety of fruits, vegetables, and certain beverages like wine and tea. However, the bioavailability and exact effects on human health can vary significantly. 3',4',7,8-TETRAMETHOXYFLAVONE, like other bioflavonoids, may have a wide array of potential health benefits and therapeutic properties that are yet to be studied in detail.

Upstream product

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Downstream Products

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Relevant articles and documents

Convenient synthesis and physiological activities of flavonoids in Coreopsis lanceolata L. petals and their related compounds

Chalcones, flavanones, and flavonols, including 8-methoxybutin isolated from Coreopsis lanceolata L. petals, were successfully synthesized with total yields of 2–59% from O-methylpyrogallols using the Horner–Wadsworth–Emmons reaction as a key reaction. Au

Substituted benzopyranones as telomerase inhibitors

The present invention relates to benzopyranone derivatives, to methods for treating telomerase-modulated diseases, in particular cancers, with said derivatives, to a process for their preparation, to their use as medicaments and to pharmaceutical compositions comprising them.

Synthesis and Pharmacological Evaluation of 2'-Hydroxychalcones and Flavones as Inhibitors of Inflammatory Mediators Generation

2'-Hydroxy-3,4-dimethoxy-3',4'-dimethylchalcone (3a), 2'-hydroxy-3',4',3,4-tetramethoxychalcone (3b), and their corresponding flavones, 3',4'-dimethoxy-7,8-dimethylflavone (4a) and 3',4',7,8-tetramethoxyflavone (4b), were prepared from 3,4-dimethoxycinnam