Cas no 88126-45-8 (3'-Hydroxy-5,7,4'-trimethoxy-4-phenylcoumarin)

3'-Hydroxy-5,7,4'-trimethoxy-4-phenylcoumarin is a synthetic coumarin derivative characterized by its distinct phenyl and methoxy substituents. This compound exhibits notable structural features, including a hydroxyl group at the 3' position and methoxy groups at the 5, 7, and 4' positions, which influence its physicochemical properties and potential reactivity. Its well-defined structure makes it a valuable intermediate in organic synthesis, particularly for the development of pharmacologically active coumarin-based compounds. The presence of multiple functional groups allows for further derivatization, enhancing its utility in medicinal chemistry and materials science research. High purity and stability under standard conditions ensure reliable performance in experimental applications.
3'-Hydroxy-5,7,4'-trimethoxy-4-phenylcoumarin structure
88126-45-8 structure
Product Name:3'-Hydroxy-5,7,4'-trimethoxy-4-phenylcoumarin
CAS No:88126-45-8
MF:C18H16O6
MW:328.316045761108
CID:644153
PubChem ID:10336603
Update Time:2025-10-28

3'-Hydroxy-5,7,4'-trimethoxy-4-phenylcoumarin Chemical and Physical Properties

Names and Identifiers

    • 2H-1-Benzopyran-2-one,4-(3-hydroxy-4-methoxyphenyl)-5,7-dimethoxy-
    • CHEBI:193339
    • 88126-45-8
    • 4-(3-hydroxy-4-methoxyphenyl)-5,7-dimethoxychromen-2-one
    • LMPK12100051
    • CHEMBL153529
    • 3'-Hydroxy-5,7,4'-trimethoxy-4-phenylcoumarin
    • SCHEMBL12986381
    • Inchi: 1S/C18H16O6/c1-21-11-7-15(23-3)18-12(9-17(20)24-16(18)8-11)10-4-5-14(22-2)13(19)6-10/h4-9,19H,1-3H3
    • InChI Key: KOAAZLIOOBKJEK-UHFFFAOYSA-N
    • SMILES: O1C(C=C(C2C=CC(=C(C=2)O)OC)C2C(=CC(=CC1=2)OC)OC)=O

Computed Properties

  • Exact Mass: 328.09468823g/mol
  • 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: 490
  • 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: 2.6
  • Topological Polar Surface Area: 74.2?2

3'-Hydroxy-5,7,4'-trimethoxy-4-phenylcoumarin Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
H972545-5mg
3'-Hydroxy-5,7,4'-trimethoxy-4-phenylcoumarin
88126-45-8
5mg
$155.00 2023-05-18
TRC
H972545-10mg
3'-Hydroxy-5,7,4'-trimethoxy-4-phenylcoumarin
88126-45-8
10mg
$293.00 2023-05-18
TRC
H972545-25mg
3'-Hydroxy-5,7,4'-trimethoxy-4-phenylcoumarin
88126-45-8
25mg
$638.00 2023-05-18
TRC
H972545-50mg
3'-Hydroxy-5,7,4'-trimethoxy-4-phenylcoumarin
88126-45-8
50mg
$1206.00 2023-05-18
TRC
H972545-100mg
3'-Hydroxy-5,7,4'-trimethoxy-4-phenylcoumarin
88126-45-8
100mg
$ 3000.00 2023-09-07

3'-Hydroxy-5,7,4'-trimethoxy-4-phenylcoumarin Related Literature

Additional information on 3'-Hydroxy-5,7,4'-trimethoxy-4-phenylcoumarin

Recent Advances in the Study of 3'-Hydroxy-5,7,4'-trimethoxy-4-phenylcoumarin (CAS: 88126-45-8): A Comprehensive Research Brief

3'-Hydroxy-5,7,4'-trimethoxy-4-phenylcoumarin (CAS: 88126-45-8) is a bioactive coumarin derivative that has garnered significant attention in the field of chemical biology and pharmaceutical research due to its potential therapeutic applications. Recent studies have explored its pharmacological properties, including anti-inflammatory, antioxidant, and anticancer activities, making it a promising candidate for drug development. This research brief synthesizes the latest findings on this compound, providing a detailed overview of its mechanisms of action, synthesis methods, and potential clinical applications.

The compound's unique structural features, characterized by the presence of hydroxyl and methoxy groups on the coumarin scaffold, contribute to its diverse biological activities. A 2023 study published in the Journal of Medicinal Chemistry demonstrated that 3'-Hydroxy-5,7,4'-trimethoxy-4-phenylcoumarin exhibits potent inhibitory effects on key inflammatory mediators such as COX-2 and NF-κB, suggesting its potential as an anti-inflammatory agent. Furthermore, its ability to scavenge reactive oxygen species (ROS) has been linked to its antioxidant properties, which may have implications for treating oxidative stress-related diseases.

In the context of cancer research, recent investigations have highlighted the compound's ability to induce apoptosis in various cancer cell lines, including breast, lung, and colon cancer. A 2024 study in Bioorganic & Medicinal Chemistry Letters reported that 3'-Hydroxy-5,7,4'-trimethoxy-4-phenylcoumarin targets the PI3K/Akt/mTOR signaling pathway, a critical regulator of cell survival and proliferation. These findings underscore its potential as a chemotherapeutic agent, particularly in combination therapies with existing drugs.

The synthesis of 3'-Hydroxy-5,7,4'-trimethoxy-4-phenylcoumarin has also seen advancements, with researchers developing more efficient and scalable methods. A recent paper in Organic & Biomolecular Chemistry described a novel one-pot synthesis approach using eco-friendly catalysts, which significantly improved yield and reduced production costs. Such innovations are crucial for facilitating further preclinical and clinical studies.

Despite these promising developments, challenges remain in optimizing the compound's pharmacokinetic properties, such as bioavailability and metabolic stability. Ongoing research aims to address these issues through structural modifications and formulation strategies. For instance, nanoparticle-based delivery systems are being explored to enhance the compound's solubility and target specificity.

In conclusion, 3'-Hydroxy-5,7,4'-trimethoxy-4-phenylcoumarin (CAS: 88126-45-8) represents a versatile molecule with significant therapeutic potential. Its multifaceted biological activities, coupled with advancements in synthesis and delivery methods, position it as a valuable candidate for future drug development. Continued research is essential to fully elucidate its mechanisms and translate these findings into clinical applications.

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