Cas no 19040-67-6 (7,8-Dihydroxy-4-propyl-2H-chromen-2-one)

7,8-Dihydroxy-4-propyl-2H-chromen-2-one is a synthetic coumarin derivative characterized by its hydroxylated aromatic ring and propyl substituent at the 4-position. This compound exhibits notable reactivity due to the presence of two adjacent phenolic hydroxyl groups, which enhance its chelating and antioxidant properties. Its structural features make it a valuable intermediate in organic synthesis, particularly for developing pharmacologically active molecules or functional materials. The propyl chain contributes to improved lipophilicity, potentially influencing bioavailability in biological systems. Analytical applications may include its use as a reference standard or probe in studies involving redox processes. Careful handling is recommended due to the potential sensitivity of the catechol moiety to oxidation.
7,8-Dihydroxy-4-propyl-2H-chromen-2-one structure
19040-67-6 structure
Product Name:7,8-Dihydroxy-4-propyl-2H-chromen-2-one
CAS No:19040-67-6
MF:C12H12O4
MW:220.221283912659
MDL:MFCD08705698
CID:123326
PubChem ID:11447325
Update Time:2025-05-24

7,8-Dihydroxy-4-propyl-2H-chromen-2-one Chemical and Physical Properties

Names and Identifiers

    • 2H-1-Benzopyran-2-one,7,8-dihydroxy-4-propyl-
    • 7,8-DIHYDROXY-4-PROPYL COUMARIN
    • 7,8-Dihydroxy-4-propyl-2H-chromen-2-one
    • 7,8-dihydroxy-4-propylchromen-2-one
    • 7,8-dihydroxy-4-propyl-coumarin
    • 7,8-Dihydroxy-4-propyl-cumarin
    • BB_NC-1806
    • 2H-1-Benzopyran-2-one, 7,8-dihydroxy-4-propyl-
    • 19040-67-6
    • FT-0751045
    • SCHEMBL15295521
    • AKOS004938591
    • DTXSID10466158
    • MFCD08705698
    • VS-10249
    • EN300-186384
    • CS-0297251
    • 7,8-Dihydroxy-4-propylcoumarin
    • MDL: MFCD08705698
    • Inchi: 1S/C12H12O4/c1-2-3-7-6-10(14)16-12-8(7)4-5-9(13)11(12)15/h4-6,13,15H,2-3H2,1H3
    • InChI Key: PHPUSFBIYOLWBJ-UHFFFAOYSA-N
    • SMILES: O1C(C=C(C2C=CC(=C(C1=2)O)O)CCC)=O

Computed Properties

  • Exact Mass: 220.07400
  • 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
  • XLogP3: 2.1
  • Topological Polar Surface Area: 66.8?2

Experimental Properties

  • Color/Form: NA
  • Density: 1.3±0.1 g/cm3
  • Melting Point: Not available
  • Boiling Point: 429.2±45.0 °C at 760 mmHg
  • Flash Point: 169.6±23.2 °C
  • Refractive Index: 1.609
  • PSA: 70.67000
  • LogP: 2.15670

7,8-Dihydroxy-4-propyl-2H-chromen-2-one Customs Data

  • HS CODE:2932209090
  • Customs Data:

    China Customs Code:

    2932209090

    Overview:

    2932209090. Other lactones. 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:

    2932209090. other lactones. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

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7,8-Dihydroxy-4-propyl-2H-chromen-2-one Suppliers

Amadis Chemical Company Limited
Gold Member
Audited Supplier Audited Supplier
(CAS:19040-67-6)7,8-Dihydroxy-4-propyl-2H-chromen-2-one
Order Number:A1145648
Stock Status:in Stock
Quantity:1g
Purity:99%
Pricing Information Last Updated:Thursday, 29 August 2024 23:02
Price ($):160.0

7,8-Dihydroxy-4-propyl-2H-chromen-2-one Related Literature

Additional information on 7,8-Dihydroxy-4-propyl-2H-chromen-2-one

Exploring the Properties and Applications of 7,8-Dihydroxy-4-propyl-2H-chromen-2-one (CAS No. 19040-67-6)

7,8-Dihydroxy-4-propyl-2H-chromen-2-one, with the CAS number 19040-67-6, is a bioactive coumarin derivative that has garnered significant attention in pharmaceutical and cosmetic research. This compound belongs to the chromen-2-one family, characterized by its unique dihydroxy and propyl substitutions, which contribute to its antioxidant and anti-inflammatory properties. Researchers are increasingly exploring its potential in skincare formulations, particularly for its ability to neutralize free radicals and combat oxidative stress—a hot topic in anti-aging and dermatology.

In recent years, the demand for natural and synthetic antioxidants like 7,8-Dihydroxy-4-propyl-2H-chromen-2-one has surged, driven by consumer interest in "clean beauty" and sustainable ingredients. Searches for "coumarin derivatives for skin health" or "natural antioxidants in cosmetics" reflect this trend. The compound's CAS 19040-67-6 is often referenced in patent filings for formulations targeting hyperpigmentation and UV-induced damage, aligning with the growing market for sun care and brightening products.

From a biochemical perspective, the dihydroxy groups at positions 7 and 8 enhance the molecule's metal-chelating capacity, making it a candidate for studying neurodegenerative diseases linked to oxidative stress. This ties into popular queries such as "neuroprotective coumarins" or "antioxidants for brain health." Additionally, the propyl side chain improves lipid solubility, a critical factor for bioavailability in drug delivery systems—a key focus area in pharmaceutical R&D.

The synthesis of 7,8-Dihydroxy-4-propyl-2H-chromen-2-one typically involves Pechmann condensation or hydroxylation protocols, topics frequently searched by chemistry students and professionals. Its structural similarity to flavonoids also positions it as a subject in comparative studies on "plant-derived bioactive compounds," another trending research theme. Analytical techniques like HPLC and NMR are essential for verifying its purity, addressing common questions about "how to identify coumarin derivatives."

Beyond therapeutics, this compound's fluorescence properties have sparked interest in material science, particularly for developing sensors. Searches for "chromen-2-one applications in biosensors" highlight this niche. Regulatory-wise, CAS 19040-67-6 is not classified as hazardous, allowing broader experimental and commercial exploration. However, researchers must adhere to ethical guidelines, especially when investigating its effects on biological systems—an aspect emphasized in peer-reviewed literature.

In conclusion, 7,8-Dihydroxy-4-propyl-2H-chromen-2-one (19040-67-6) exemplifies the intersection of chemistry, medicine, and cosmetics. Its multifaceted applications respond to contemporary demands for multifunctional ingredients, while ongoing studies continue to uncover new potentials. For those exploring "innovative coumarin uses" or "next-gen antioxidant agents," this compound remains a compelling case study.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:19040-67-6)7,8-Dihydroxy-4-propyl-2H-chromen-2-one
A1145648
Purity:99%
Quantity:1g
Price ($):160.0
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