Cas no 263365-51-1 (3-Hydroxy-7,2',4'-trimethoxyflavone)

3-Hydroxy-7,2',4'-trimethoxyflavone is a flavonoid derivative characterized by its distinct methoxy and hydroxyl substitutions on the flavone backbone. This compound exhibits notable stability due to its methoxy groups, which enhance its resistance to oxidative degradation. Its structural features contribute to potential biological activity, including antioxidant and anti-inflammatory properties, making it of interest in pharmacological and biochemical research. The presence of the hydroxy group at the 3-position allows for further functionalization, broadening its utility in synthetic applications. Analytical techniques such as HPLC and NMR confirm its high purity, ensuring reliability for research purposes. Its well-defined structure and functional group versatility make it a valuable reference standard in flavonoid studies.
3-Hydroxy-7,2',4'-trimethoxyflavone structure
263365-51-1 structure
Product Name:3-Hydroxy-7,2',4'-trimethoxyflavone
CAS No:263365-51-1
MF:C18H16O6
MW:328.316045761108
CID:92640
PubChem ID:688717
Update Time:2025-11-02

3-Hydroxy-7,2',4'-trimethoxyflavone Chemical and Physical Properties

Names and Identifiers

    • 3-Hydroxy-2',4',7-trimethoxyflavone
    • 2-(2,4-dimethoxyphenyl)-3-hydroxy-7-methoxychromen-4-one
    • 3-HYDROXY-7,2',4'-TRIMETHOXYFLAVONE
    • DTXSID70350968
    • 263365-51-1
    • SCHEMBL4649979
    • MFCD02093238
    • 2-(2, 4-dimethoxyphenyl)-3-hydroxy-7-methoxychromen-4-one
    • CPSQIOPVWINXFH-UHFFFAOYSA-N
    • 4H-1-Benzopyran-4-one, 2-(2,4-dimethoxyphenyl)-3-hydroxy-7-methoxy-
    • 2-(2,4-Dimethoxyphenyl)-3-hydroxy-7-methoxy-4H-chromen-4-one
    • AKOS024282448
    • 3-Hydroxy-7,2',4'-trimethoxyflavone
    • MDL: MFCD02093238
    • Inchi: 1S/C18H16O6/c1-21-10-5-7-13(14(8-10)23-3)18-17(20)16(19)12-6-4-11(22-2)9-15(12)24-18/h4-9,20H,1-3H3
    • InChI Key: CPSQIOPVWINXFH-UHFFFAOYSA-N
    • SMILES: O1C2C=C(C=CC=2C(C(=C1C1C=CC(=CC=1OC)OC)O)=O)OC

Computed Properties

  • Exact Mass: 328.09500
  • Monoisotopic Mass: 328.09468823g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 24
  • Rotatable Bond Count: 4
  • Complexity: 502
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.3
  • Topological Polar Surface Area: 74.2?2

Experimental Properties

  • PSA: 78.13000
  • LogP: 3.19140

3-Hydroxy-7,2',4'-trimethoxyflavone Customs Data

  • HS CODE:2932999099
  • Customs Data:

    China Customs Code:

    2932999099

    Overview:

    2932999099. Other heterocyclic compounds containing only oxygen heteroatoms. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2932999099. other heterocyclic compounds with oxygen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

3-Hydroxy-7,2',4'-trimethoxyflavone Pricemore >>

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Additional information on 3-Hydroxy-7,2',4'-trimethoxyflavone

Exploring the Potential of 3-Hydroxy-7,2',4'-trimethoxyflavone (CAS No. 263365-51-1): A Comprehensive Review

In recent years, the scientific community has shown growing interest in flavonoids, a class of naturally occurring compounds known for their diverse biological activities. Among these, 3-Hydroxy-7,2',4'-trimethoxyflavone (CAS No. 263365-51-1) has emerged as a subject of significant research due to its unique structural properties and potential health benefits. This article delves into the molecular characteristics, sources, and applications of this compound, while addressing common queries such as "what is 3-Hydroxy-7,2',4'-trimethoxyflavone used for" and "how does 3-Hydroxy-7,2',4'-trimethoxyflavone work."

The chemical structure of 3-Hydroxy-7,2',4'-trimethoxyflavone features a flavone backbone with hydroxyl and methoxy substitutions at specific positions, which contribute to its distinct physicochemical properties. Researchers have identified this compound in certain medicinal plants, sparking interest in its potential role in traditional medicine and modern therapeutic applications. Studies suggest it may interact with cellular pathways related to oxidative stress and inflammation, aligning with current trends in natural product research and nutraceutical development.

From a pharmacological perspective, investigations into 3-Hydroxy-7,2',4'-trimethoxyflavone have explored its possible bioactive properties. Preliminary findings indicate it may influence enzyme activity and cell signaling, making it relevant to discussions about "natural alternatives for health support" – a topic frequently searched in connection with dietary supplements and functional foods. Its structural similarity to other phytoestrogens has also prompted studies examining potential hormone-modulating effects, though further clinical validation is required.

The analytical characterization of 3-Hydroxy-7,2',4'-trimethoxyflavone typically involves advanced techniques such as HPLC, mass spectrometry, and NMR spectroscopy. These methods help researchers address questions like "how to identify 3-Hydroxy-7,2',4'-trimethoxyflavone" and "how pure is commercial 3-Hydroxy-7,2',4'-trimethoxyflavone." Quality control remains crucial for research applications, particularly when studying its potential structure-activity relationships and possible synergistic effects with other plant-derived compounds.

Current research trends connect 3-Hydroxy-7,2',4'-trimethoxyflavone to broader discussions about plant-based therapeutics and sustainable medicine. As consumers increasingly search for "natural anti-inflammatory compounds" and "plant extracts for wellness," this flavone represents an interesting candidate for further investigation. However, scientists emphasize the need for more comprehensive studies to fully understand its mechanisms of action, bioavailability, and potential applications in nutraceutical formulations or cosmeceutical products.

In the context of drug discovery, 3-Hydroxy-7,2',4'-trimethoxyflavone serves as a valuable lead compound for structural modification and optimization. Its molecular scaffold offers opportunities for developing derivatives with enhanced pharmacokinetic properties or targeted biological activities. This aligns with growing interest in "flavonoids as therapeutic agents" and "natural product drug development" – topics that frequently appear in scientific literature and patent applications.

From a commercial perspective, the availability of 3-Hydroxy-7,2',4'-trimethoxyflavone as a research chemical has facilitated various in vitro and in vivo studies. Suppliers often highlight its high purity grade and provide detailed analytical certificates, addressing common purchaser concerns about "where to buy authentic 3-Hydroxy-7,2',4'-trimethoxyflavone." The compound's stability profile and solubility characteristics are also frequently discussed among researchers working on formulation development.

Looking ahead, the scientific exploration of 3-Hydroxy-7,2',4'-trimethoxyflavone continues to evolve, with new studies examining its potential role in various biological systems. As interest grows in personalized nutrition and precision medicine, this compound may gain further attention for its possible health-modulating effects. Future research directions likely include more detailed investigations of its molecular targets, potential clinical applications, and optimization for improved therapeutic efficacy.

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