Cas no 66346-59-6 (5,7-Dihydroxy-4-propyl-2H-chromen-2-one)

5,7-Dihydroxy-4-propyl-2H-chromen-2-one structure
66346-59-6 structure
Product Name:5,7-Dihydroxy-4-propyl-2H-chromen-2-one
CAS No:66346-59-6
MF:C12H12O4
MW:220.221283912659
MDL:MFCD01472300
CID:1003762
PubChem ID:5391260
Update Time:2025-07-18

5,7-Dihydroxy-4-propyl-2H-chromen-2-one Chemical and Physical Properties

Names and Identifiers

    • 5,7-DIHYDROXY-4-PROPYLCOUMARIN AKYL (OR ARYL) COUMARINS
    • 5 7-DIHYDROXY-4-PROPYLCOUMARIN 98
    • 5,7-DIHYDROXY-4-PROPYL-CHROMEN-2-ONE
    • 5,7-DIHYDROXY-4-PROPYL COUMARIN
    • 5,7-Dihydroxy-4-propyl-2H-chromen-2-one
    • 4-propyl-5,7-dihydroxycoumarin
    • 5,7-Dihydroxy-4-(n-propyl)coumarin
    • 5,7-dihydroxy-4-propyl-2H-1-benzopyran-2-one
    • 5,7-Dihydroxy-4propyl-2H-1-benzopyran-2-one
    • AC1NTZ65
    • CHEMBL591687
    • CTK5C4325
    • IFLab1_001705
    • Oprea1_823829
    • 5 7-DIHYDROXY-4-PROPYLCOUMARIN 98
    • 5,7-Dihydroxy-4-propylcoumarin
    • SR-01000219501
    • 5,7-dihydroxy-4propyl-coumarin
    • 5,7-dihydroxy4-propylcoumarin
    • SCHEMBL3775925
    • BBL029377
    • 5.7-dihydroxy-4-propyl-coumarin
    • EN300-302359
    • HMS1416N11
    • AB00096404-01
    • DTXSID30419808
    • 5,7-dihydroxy4propylcoumarin
    • 4-n-propyl-5,7-dihydroxy-coumarin
    • AS-63001
    • STL372192
    • AKOS002347433
    • MFCD01472300
    • 5,7-Dihydroxy-4-n-propylcoumarin
    • HDPADVKOPBBPJW-UHFFFAOYSA-N
    • SR-01000219501-1
    • 5,7-dihydroxy-4-propyl-coumarin
    • 5,7-Dihydroxy-4-propylcoumarin, 98%
    • 5,7-dihydroxy-4-propylchromen-2-one
    • CS-0297253
    • 66346-59-6
    • AS-871/11436323
    • MDL: MFCD01472300
    • Inchi: 1S/C12H12O4/c1-2-3-7-4-11(15)16-10-6-8(13)5-9(14)12(7)10/h4-6,13-14H,2-3H2,1H3
    • InChI Key: HDPADVKOPBBPJW-UHFFFAOYSA-N
    • SMILES: O1C(C=C(C2C(=CC(=CC1=2)O)O)CCC)=O

Computed Properties

  • Exact Mass: 220.07355886g/mol
  • Monoisotopic Mass: 220.07355886g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 2
  • Complexity: 310
  • 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
  • Surface Charge: 0
  • Tautomer Count: 33
  • XLogP3: 2.1
  • Topological Polar Surface Area: 66.8?2

Experimental Properties

  • Color/Form: solid
  • Density: 1.3±0.1 g/cm3
  • Melting Point: 239?°C (dec.)(lit.)
  • Boiling Point: 470.1±14.0 °C at 760 mmHg
  • Flash Point: 188.5±13.6 °C
  • Refractive Index: 1.698
  • PSA: 70.67000
  • LogP: 2.15670
  • Solubility: Not available
  • Vapor Pressure: 0.0±1.2 mmHg at 25°C

5,7-Dihydroxy-4-propyl-2H-chromen-2-one Security Information

5,7-Dihydroxy-4-propyl-2H-chromen-2-one Pricemore >>

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5,7-Dihydroxy-4-propyl-2H-chromen-2-one Related Literature

  • 1. Synthesis of the Mammea coumarins. Part 2. Experiments in the mammea E series and synthesis of mammea E/AC
    Leslie Crombie,Raymond C. F. Jones,Christopher J. Palmer J. Chem. Soc. Perkin Trans. 1 1987 333
  • 2. Synthesis of the Mammea coumarins. Part 1. The coumarins of the mammea A, B, and C series
    Leslie Crombie,Raymond C. F. Jones,Christopher J. Palmer J. Chem. Soc. Perkin Trans. 1 1987 317
  • 3. Synthesis of the Mammea coumarins. Part 4. Stereochemical and regiochemical studies, and synthesis of (–)-mammea B/BB
    Michael J. Begley,Leslie Crombie,Raymond C. F. Jones,Christopher J. Palmer J. Chem. Soc. Perkin Trans. 1 1987 353

Additional information on 5,7-Dihydroxy-4-propyl-2H-chromen-2-one

Comprehensive Overview of 5,7-Dihydroxy-4-propyl-2H-chromen-2-one (CAS No. 66346-59-6)

5,7-Dihydroxy-4-propyl-2H-chromen-2-one, a naturally occurring coumarin derivative, has garnered significant attention in recent years due to its potential applications in pharmaceuticals, cosmetics, and nutraceuticals. With the growing interest in plant-based bioactive compounds, this molecule stands out for its unique structural properties and biological activities. Researchers and industry professionals are increasingly exploring its benefits, particularly in the context of antioxidant, anti-inflammatory, and skin-protective effects, aligning with the rising demand for natural and sustainable ingredients.

The compound, identified by CAS No. 66346-59-6, belongs to the coumarin family, a class of organic compounds known for their diverse pharmacological properties. Coumarins have been extensively studied for their role in drug discovery and functional foods, making 5,7-Dihydroxy-4-propyl-2H-chromen-2-one a subject of interest for both academic and industrial research. Its molecular structure, featuring a propyl substituent and two hydroxyl groups, contributes to its solubility and reactivity, which are critical for its bioavailability and efficacy.

In the realm of cosmetic science, 5,7-Dihydroxy-4-propyl-2H-chromen-2-one is being investigated for its potential to combat oxidative stress, a key factor in skin aging. Modern consumers are increasingly seeking products with natural antioxidants to replace synthetic additives, driving demand for ingredients like this coumarin derivative. Studies suggest that it may help neutralize free radicals, thereby protecting the skin from environmental damage and promoting a youthful appearance. This aligns with the global trend toward clean beauty and sustainable skincare solutions.

Another area of interest is the compound's potential role in nutraceuticals. As the health and wellness industry expands, there is a growing focus on bioactive compounds that can support overall well-being. 5,7-Dihydroxy-4-propyl-2H-chromen-2-one has shown promise in preliminary studies for its ability to modulate inflammatory pathways, which could make it a valuable ingredient in dietary supplements targeting chronic inflammation—a common concern among health-conscious consumers. Its compatibility with plant-based diets and vegan formulations further enhances its appeal.

From a pharmaceutical perspective, this coumarin derivative is being explored for its potential therapeutic applications. While research is still in the early stages, its structural similarity to other bioactive coumarins suggests it may have antimicrobial or neuroprotective properties. These attributes are particularly relevant in the context of emerging health challenges, such as antibiotic resistance and neurodegenerative diseases, which are frequently searched topics in scientific and medical communities.

The synthesis and extraction of 5,7-Dihydroxy-4-propyl-2H-chromen-2-one are also topics of interest. Advances in green chemistry and sustainable extraction methods have made it possible to obtain this compound with minimal environmental impact. This resonates with the broader shift toward eco-friendly manufacturing practices, a priority for both regulators and consumers. Researchers are optimizing techniques to improve yield and purity, ensuring that the compound meets the stringent standards required for commercial use.

In summary, 5,7-Dihydroxy-4-propyl-2H-chromen-2-one (CAS No. 66346-59-6) represents a promising bioactive compound with multifaceted applications. Its relevance to antioxidant research, cosmetic innovation, and nutraceutical development positions it as a valuable subject for ongoing study. As scientific understanding of its mechanisms and benefits grows, so too will its potential to address some of the most pressing needs in health, wellness, and sustainability.

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