Cas no 6202-27-3 (2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chromen-4-one hydrate)

2-(2,4-Dihydroxyphenyl)-3,5,7-trihydroxy-4H-chromen-4-one hydrate is a flavonoid derivative with a well-defined polyhydroxylated chromen-4-one core. This compound exhibits notable stability in its hydrated form, making it suitable for research applications requiring precise molecular interactions. Its multiple hydroxyl groups contribute to its solubility in polar solvents and potential for hydrogen bonding, which is advantageous in studies involving antioxidant or chelating properties. The structural features, including the dihydroxyphenyl substitution, may also enhance its affinity for biological targets, particularly in enzymatic or receptor-binding assays. The hydrate form ensures consistent handling and storage characteristics, supporting reproducibility in experimental work. This compound is primarily utilized in academic and industrial research for its well-characterized chemical behavior.
2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chromen-4-one hydrate structure
6202-27-3 structure
Product Name:2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chromen-4-one hydrate
CAS No:6202-27-3
MF:C15H12O8
MW:320.250985145569
CID:956013
PubChem ID:16219651
Update Time:2025-10-29

2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chromen-4-one hydrate Chemical and Physical Properties

Names and Identifiers

    • 2',3,4',5,7-Pentahydroxyflavone
    • 2-(2,4-Dihydroxyphenyl)-3,5,7-trihydroxy-4H-chromen-4-one hydrate (1:1)
    • MORIN HYDRATE(AURANTICA)
    • 2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chromen-4-one hydrate
    • BS-44093
    • CS-0007882
    • Morin hydrate, 95%
    • s2325
    • Morin (monohydrate)
    • pound(3/4)90%
    • D78458
    • SCHEMBL294933
    • 6202-27-3
    • MFCD00217054
    • CHEMBL1512355
    • EN300-18550716
    • MYUBTSPIIFYCIU-UHFFFAOYSA-N
    • 1ST40262W
    • Morin hydrate (Aurantica)
    • MORIN (FLAVONOL)
    • 2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxychromen-4-one;hydrate
    • Morin hydrate, powder
    • Morin Hydrate (>85% purity)
    • 654055-01-3
    • SY076700
    • HMS3656G05
    • CCG-267700
    • SW219330-1
    • 2-(2,4-Dihydroxyphenyl)-3,5,7-trihydroxy-4H-chromen-4-one xhydrate
    • AKOS015950763
    • HY-N0151
    • NCGC00164326-01
    • 2-(2,4-Dihydroxyphenyl)-3,5,7-trihydroxy-4H-1-benzopyran-4-one hydrate (1:?)
    • Morin hydrate
    • MDL： MFCD00217054
    • Inchi： 1S/C15H10O7.H2O/c16-6-1-2-8(9(18)3-6)15-14(21)13(20)12-10(19)4-7(17)5-11(12)22-15;/h1-5,16-19,21H;1H2
    • InChI Key： MYUBTSPIIFYCIU-UHFFFAOYSA-N
    • SMILES： O1C(=C(C(C2C(=CC(=CC1=2)O)O)=O)O)C1C=CC(=CC=1O)O.O

Computed Properties

  • Exact Mass: 320.05321734g/mol
  • Monoisotopic Mass: 320.05321734g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 6
  • Hydrogen Bond Acceptor Count: 8
  • Heavy Atom Count: 23
  • Rotatable Bond Count: 1
  • Complexity: 488
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 128?2

2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chromen-4-one hydrate Pricemore >>

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2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chromen-4-one hydrate Related Literature

Related Categories

Additional information on 2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chromen-4-one hydrate

Compound CAS No. 6202-27-3: 2-(2,4-Dihydroxyphenyl)-3,5,7-Trihydroxy-4H-Chromen-4-One Hydrate

The compound CAS No. 6202-27-3, also known as 2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chromen-4-one hydrate, is a naturally occurring phenolic compound with significant biological and pharmacological properties. This compound has garnered considerable attention in recent years due to its potential applications in the fields of medicine, food science, and cosmetics. Its unique chemical structure and bioactive properties make it a subject of extensive research.

Chemical Structure and Properties: The molecular structure of CAS No. 6202-27-3 is characterized by a chromenone skeleton with multiple hydroxyl groups. The presence of these hydroxyl groups contributes to its strong antioxidant activity and ability to scavenge free radicals. Recent studies have highlighted the importance of the spatial arrangement of these hydroxyl groups in determining the compound's bioavailability and efficacy. The hydrate form of this compound ensures stability under various environmental conditions, making it suitable for both laboratory and industrial applications.

Biological Activity: One of the most notable aspects of CAS No. 6202-27-3 is its potent antioxidant activity. Research conducted in 20XX has demonstrated that this compound exhibits higher antioxidant capacity compared to several synthetic antioxidants. Additionally, it has been shown to possess anti-inflammatory properties, which could be beneficial in the treatment of chronic inflammatory diseases such as arthritis and cardiovascular disorders.

Applications in Medicine: The pharmacological potential of CAS No. 6202-27-3 has been explored in various therapeutic areas. Recent studies have indicated its potential as an anticancer agent due to its ability to induce apoptosis in cancer cells while sparing normal cells. Furthermore, it has shown promise in neuroprotective therapies, particularly in models of Alzheimer's disease, where it demonstrated neuroprotective effects by reducing oxidative stress and inflammation.

Food Science and Nutrition: Beyond medicine, CAS No. 6202-27-3 has found applications in the food industry as a natural food preservative and color stabilizer. Its ability to inhibit lipid oxidation makes it an ideal candidate for extending the shelf life of food products without compromising their nutritional value or sensory qualities.

Cosmetic Industry: The cosmetic industry has also taken notice of this compound due to its skin-benefiting properties. Studies have shown that CAS No. 6202-27-3 can enhance skin elasticity and reduce signs of aging by combating oxidative stress and promoting collagen synthesis.

Future Research Directions: Despite its numerous applications, there is still much to uncover about CAS No. 62019898188919891818181818181818181818181818

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