Cas no 200400-76-6 (Ethyl 2-(4'-Hydroxyphenyl)-1,3-oxazole-4-carboxylate)

Ethyl 2-(4'-Hydroxyphenyl)-1,3-oxazole-4-carboxylate is a specialized oxazole derivative with a hydroxyl-substituted phenyl ring at the 2-position and an ester functional group at the 4-position. This compound is of interest in organic synthesis and medicinal chemistry due to its versatile reactivity, serving as a key intermediate for the development of heterocyclic compounds. The presence of both the hydroxyl and ester groups allows for further functionalization, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its structural features contribute to potential biological activity, particularly in applications requiring aromatic and heterocyclic frameworks. The compound exhibits stability under standard handling conditions, ensuring reliable performance in synthetic workflows.
Ethyl 2-(4'-Hydroxyphenyl)-1,3-oxazole-4-carboxylate structure
200400-76-6 structure
Product Name:Ethyl 2-(4'-Hydroxyphenyl)-1,3-oxazole-4-carboxylate
CAS No:200400-76-6
MF:C12H11NO4
MW:233.220043420792
MDL:MFCD02183587
CID:66580
PubChem ID:2758854
Update Time:2025-10-30

Ethyl 2-(4'-Hydroxyphenyl)-1,3-oxazole-4-carboxylate Chemical and Physical Properties

Names and Identifiers

    • Ethyl 2-(4-hydroxyphenyl)oxazole-4-carboxylate
    • 2-(4-hydroxyphenyl)-4-Oxazolecarboxylic acid ethyl ester
    • 2-(4-HYDROXY-PHENYL)-OXAZOLE-4-CARBOXYLIC ACID ETHYL ESTER
    • ethyl 2-(4-oxocyclohexa-2,5-dien-1-ylidene)-3H-1,3-oxazole-4-carboxylate
    • 2-(2-METHYLPHENOXY)ETHYL]HYDRAZINE HYDROCHLORIDE
    • Ethyl 2-(4'-hydroxyphenyl)-1,3-oxazole-4-carboxylate
    • Ethyl 2-(4-hydroxyphenyl)-1,3-oxazole-4-carboxylate
    • Ethyl2-(4-hydroxyphenyl)oxazole-4-carboxylate
    • AKOS015843419
    • AC-6425
    • FT-0687240
    • Ethyl 2-(4-oxocyclohexa-2,5-dien-1-ylidene)-2,3-dihydro-1,3-oxazole-4-carboxylate
    • MFCD02183587
    • 200400-76-6
    • CS-0172329
    • ethyl 2-(4-hydroxyphenyl)-1, 3-oxazole-4-carboxylate
    • 4-Oxazolecarboxylic acid, 2-(4-hydroxyphenyl)-, ethyl ester
    • SCHEMBL3070077
    • AB11532
    • XILWQVZWGWQRNU-UHFFFAOYSA-N
    • AMY1750
    • AS-46710
    • Q-102357
    • DTXSID80420702
    • Ethyl 2-(4-Hy droxyphenyl)oxazole-4-carboxylate
    • E58685
    • Ethyl 2-(4''-Hydroxyphenyl)-1,3-oxazole-4-carboxylate
    • DB-031684
    • Ethyl 2-(4'-Hydroxyphenyl)-1,3-oxazole-4-carboxylate
    • MDL： MFCD02183587
    • Inchi： 1S/C12H11NO4/c1-2-16-12(15)10-7-17-11(13-10)8-3-5-9(14)6-4-8/h3-7,14H,2H2,1H3
    • InChI Key： XILWQVZWGWQRNU-UHFFFAOYSA-N
    • SMILES： O1C=C(C(=O)OCC)N=C1C1C=CC(=CC=1)O

Computed Properties

  • Exact Mass: 233.06900
  • Monoisotopic Mass: 233.06880783g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 17
  • Rotatable Bond Count: 4
  • Complexity: 263
  • 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: 2.2
  • Topological Polar Surface Area: 72.6?2

Experimental Properties

  • Color/Form: White to Yellow Solid
  • Density: 1.27
  • Boiling Point: 399 °C at 760 mmHg
  • Flash Point: 195.1 °C
  • PSA: 72.56000
  • LogP: 2.22390
  • Vapor Pressure: 0.0±1.0 mmHg at 25°C

Ethyl 2-(4'-Hydroxyphenyl)-1,3-oxazole-4-carboxylate Security Information

Ethyl 2-(4'-Hydroxyphenyl)-1,3-oxazole-4-carboxylate Customs Data

  • HS CODE：2934999090
  • Customs Data：

    China Customs Code:

    2934999090

    Overview:

    2934999090. Other heterocyclic compounds. 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:

    2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Ethyl 2-(4'-Hydroxyphenyl)-1,3-oxazole-4-carboxylate Pricemore >>

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Ethyl 2-(4'-Hydroxyphenyl)-1,3-oxazole-4-carboxylate Related Literature

Additional information on Ethyl 2-(4'-Hydroxyphenyl)-1,3-oxazole-4-carboxylate

Comprehensive Overview of Ethyl 2-(4'-Hydroxyphenyl)-1,3-oxazole-4-carboxylate (CAS No. 200400-76-6)

Ethyl 2-(4'-Hydroxyphenyl)-1,3-oxazole-4-carboxylate (CAS No. 200400-76-6) is a specialized organic compound that has garnered significant attention in pharmaceutical and agrochemical research. This compound belongs to the oxazole family, a class of heterocyclic compounds known for their diverse biological activities. The presence of both a hydroxyphenyl group and an ester functionality in its structure makes it a versatile intermediate for synthesizing more complex molecules. Researchers are particularly interested in its potential applications in drug discovery, given its structural similarity to bioactive molecules.

In recent years, the demand for Ethyl 2-(4'-Hydroxyphenyl)-1,3-oxazole-4-carboxylate has increased due to its role in developing antioxidant and anti-inflammatory agents. The 4'-hydroxyphenyl moiety is a key feature that contributes to its radical-scavenging properties, making it a candidate for studies on oxidative stress-related diseases. Additionally, its oxazole core is often explored in the design of antimicrobial and anticancer compounds, aligning with current trends in medicinal chemistry.

The synthesis of Ethyl 2-(4'-Hydroxyphenyl)-1,3-oxazole-4-carboxylate typically involves condensation reactions, with researchers optimizing conditions for higher yields and purity. Its CAS number 200400-76-6 is frequently searched in chemical databases, reflecting its relevance in academic and industrial settings. Questions like "How to synthesize Ethyl 2-(4'-Hydroxyphenyl)-1,3-oxazole-4-carboxylate?" or "What are the biological activities of oxazole derivatives?" are common among chemists and pharmacologists, indicating its growing importance.

From an industrial perspective, this compound is valued for its potential in green chemistry applications. Its derivatives are being investigated as eco-friendly alternatives in crop protection, addressing the global push for sustainable agriculture. The ester group in its structure allows for further functionalization, enabling the creation of tailored molecules for specific agrochemical needs. This aligns with the increasing focus on biodegradable and low-toxicity solutions in farming.

In summary, Ethyl 2-(4'-Hydroxyphenyl)-1,3-oxazole-4-carboxylate (CAS No. 200400-76-6) is a multifaceted compound with promising applications in pharmaceuticals, agrochemicals, and material science. Its unique structure and reactivity profile make it a subject of ongoing research, particularly in the context of drug development and sustainable chemistry. As scientific inquiries into its properties expand, this compound is likely to remain a key player in innovative chemical solutions.

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