Cas no 24724-52-5 (7H-Furo[3,2-g][1]benzopyran-7-one, 4-(2,3-dihydroxy-3-methylbutoxy)-)

7H-Furo[3,2-g][1]benzopyran-7-one, 4-(2,3-dihydroxy-3-methylbutoxy)-, is a furanocoumarin derivative characterized by its unique fused benzopyranone structure with a dihydroxy-3-methylbutoxy substituent. This compound exhibits notable photochemical reactivity, making it valuable in studies involving UV-induced reactions and photobiological applications. Its structural features, including the hydroxyl groups, enhance solubility in polar solvents, facilitating its use in synthetic and mechanistic research. The molecule’s potential as a precursor for bioactive analogs is of interest due to the coumarin scaffold’s prevalence in pharmaceuticals. Its well-defined chemical properties support precise analytical and experimental work in organic chemistry and photodynamic research.
7H-Furo[3,2-g][1]benzopyran-7-one, 4-(2,3-dihydroxy-3-methylbutoxy)- structure
24724-52-5 structure
Product Name:7H-Furo[3,2-g][1]benzopyran-7-one, 4-(2,3-dihydroxy-3-methylbutoxy)-
CAS No:24724-52-5
MF:C16H16O6
MW:304.294645309448
MDL:MFCD00603834
CID:1418360
PubChem ID:483513
Update Time:2025-06-14

7H-Furo[3,2-g][1]benzopyran-7-one, 4-(2,3-dihydroxy-3-methylbutoxy)- Chemical and Physical Properties

Names and Identifiers

    • 7H-Furo[3,2-g][1]benzopyran-7-one, 4-(2,3-dihydroxy-3-methylbutoxy)-
    • 4-(2,3-dihydroxy-3-methylbutoxy)furo[3,2-g]chromen-7-one
    • 5-(2,3-Dihydroxy-3-methylbutoxy)psoralen
    • 4-(2,3-Dihydroxy-3-methylbutoxy)-7H-furo[3,2-g][1]benzopyran-7-one
    • PEWFWDOPJISUOK-UHFFFAOYSA-N
    • BRD-A22947368-001-01-7
    • 4-(2,3-Dihydroxy-3-methylbutoxy)-7H-furo[3,2-g]chromen-7-one #
    • B2703-477521
    • B2703-464765
    • 4-(2,3-dihydroxy-3-methyl-butoxy)furo[3,2-g]chromen-7-one
    • MEGxp0_000084
    • HMS3347D15
    • ACon1_000447
    • 24724-52-5
    • FT-0777292
    • 4-(2,3-Dihydroxy-3-methylbutoxy)furo(3,2-g)chromen-7-one
    • SMR000440613
    • Oprea1_033750
    • 4-(2,3-dihydroxy-3-methylbutoxy)uro[3,2-g]chromen-7-one
    • DTXSID10333114
    • SCHEMBL15944413
    • Oxypeucedaninhydrate
    • FT-0775574
    • NCGC00169070-01
    • CHEMBL1438253
    • AKOS003601375
    • Oprea1_667233
    • HMS2267N05
    • MLS000877013
    • CHEBI:177798
    • (+)-Aviprin
    • Prangolarin hydrate
    • Oxypeucedanin hydrate
    • MDL: MFCD00603834
    • Inchi: 1S/C16H16O6/c1-16(2,19)13(17)8-21-15-9-3-4-14(18)22-12(9)7-11-10(15)5-6-20-11/h3-7,13,17,19H,8H2,1-2H3
    • InChI Key: PEWFWDOPJISUOK-UHFFFAOYSA-N
    • SMILES: O(C1=C2C=CC(=O)OC2=CC2=C1C=CO2)CC(C(C)(C)O)O

Computed Properties

  • Exact Mass: 304.09468
  • Monoisotopic Mass: 304.09468823g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 22
  • Rotatable Bond Count: 4
  • Complexity: 460
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1.6
  • Topological Polar Surface Area: 89.1?2

Experimental Properties

  • Density: 1.386
  • PSA: 89.13

7H-Furo[3,2-g][1]benzopyran-7-one, 4-(2,3-dihydroxy-3-methylbutoxy)- Pricemore >>

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7H-Furo[3,2-g][1]benzopyran-7-one, 4-(2,3-dihydroxy-3-methylbutoxy)- Related Literature

Additional information on 7H-Furo[3,2-g][1]benzopyran-7-one, 4-(2,3-dihydroxy-3-methylbutoxy)-

Comprehensive Analysis of 7H-Furo[3,2-g][1]benzopyran-7-one, 4-(2,3-dihydroxy-3-methylbutoxy)- (CAS No. 24724-52-5)

The compound 7H-Furo[3,2-g][1]benzopyran-7-one, 4-(2,3-dihydroxy-3-methylbutoxy)- (CAS No. 24724-52-5) is a specialized organic molecule that has garnered significant attention in the fields of pharmaceutical research and natural product chemistry. This compound belongs to the furocoumarin family, a class of molecules known for their unique photochemical properties and potential therapeutic applications. Researchers are particularly interested in its structural features, which include a furan ring fused to a benzopyranone core, along with a dihydroxy-3-methylbutoxy side chain. These characteristics make it a promising candidate for further study in drug development and bioactive compound synthesis.

In recent years, the demand for natural-derived compounds with medicinal properties has surged, driven by the growing interest in alternative therapies and sustainable healthcare solutions. 7H-Furo[3,2-g][1]benzopyran-7-one, 4-(2,3-dihydroxy-3-methylbutoxy)- has been identified as a potential key player in this space due to its structural similarity to other bioactive coumarin derivatives. Scientists are exploring its possible roles in anti-inflammatory, antioxidant, and enzyme inhibition applications, which align with current trends in precision medicine and personalized healthcare.

The synthesis and characterization of CAS No. 24724-52-5 involve advanced techniques such as nuclear magnetic resonance (NMR) spectroscopy and high-performance liquid chromatography (HPLC). These methods ensure the purity and consistency of the compound, which is critical for its use in research and development. Additionally, the compound's solubility and stability under various conditions are being studied to optimize its formulation for potential commercial applications. This aligns with the broader industry focus on green chemistry and eco-friendly synthesis methods.

One of the most frequently asked questions about 7H-Furo[3,2-g][1]benzopyran-7-one, 4-(2,3-dihydroxy-3-methylbutoxy)- is its potential role in skin care and cosmeceuticals. Given the rising popularity of plant-based ingredients in the beauty industry, this compound's photochemical properties could make it a valuable addition to formulations targeting UV protection or anti-aging. However, further clinical studies are needed to validate these applications.

From a commercial perspective, the global market for specialty chemicals and fine chemicals is expanding, with increasing investments in research and development (R&D). CAS No. 24724-52-5 represents a niche but growing segment, particularly in the pharmaceutical intermediates and nutraceutical ingredients sectors. Companies specializing in custom synthesis and contract manufacturing are actively exploring its production scalability to meet potential demand.

In conclusion, 7H-Furo[3,2-g][1]benzopyran-7-one, 4-(2,3-dihydroxy-3-methylbutoxy)- (CAS No. 24724-52-5) is a compound of significant scientific and commercial interest. Its unique structure, combined with the growing demand for bioactive natural products, positions it as a promising candidate for future innovations in healthcare, cosmetics, and material science. As research progresses, this compound may unlock new possibilities in drug discovery and sustainable chemistry.

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