Cas no 109604-76-4 (Phenol, 2-(2-oxazolyl)-)

Phenol, 2-(2-oxazolyl)- structure
Phenol, 2-(2-oxazolyl)- structure
Product Name:Phenol, 2-(2-oxazolyl)-
CAS No:109604-76-4
MF:C9H7NO2
MW:161.157382249832
MDL:MFCD24715197
CID:1188737
PubChem ID:135686401
Update Time:2025-07-22

Phenol, 2-(2-oxazolyl)- Chemical and Physical Properties

Names and Identifiers

    • Phenol, 2-(2-oxazolyl)-
    • 6-(3H-1,3-oxazol-2-ylidene)cyclohexa-2,4-dien-1-one
    • 2-(1,3-oxazol-2-yl)phenol
    • SCHEMBL243773
    • 109604-76-4
    • 2-(2'-hydroxyphenyl)oxazole
    • 2-(oxazol-2-yl)phenol
    • DB-408001
    • DTXSID70709391
    • 6-(1,3-Oxazol-2(3H)-ylidene)cyclohexa-2,4-dien-1-one
    • o-hydroxyphenyloxazole
    • MDL: MFCD24715197
    • Inchi: 1S/C9H7NO2/c11-8-4-2-1-3-7(8)9-10-5-6-12-9/h1-6,11H
    • InChI Key: OKJDRGLFCIXKST-UHFFFAOYSA-N
    • SMILES: O1C=CN=C1C1C=CC=CC=1O

Computed Properties

  • Exact Mass: 161.047678466g/mol
  • Monoisotopic Mass: 161.047678466g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 1
  • Complexity: 152
  • 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: 1.6
  • Topological Polar Surface Area: 46.3?2

Phenol, 2-(2-oxazolyl)- Pricemore >>

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Additional information on Phenol, 2-(2-oxazolyl)-

Phenol, 2-(2-oxazolyl)- (CAS No. 109604-76-4): A Comprehensive Overview in Modern Chemical and Pharmaceutical Research

Phenol, 2-(2-oxazolyl)-, identified by its Chemical Abstracts Service (CAS) number 109604-76-4, is a significant compound in the realm of chemical and pharmaceutical research. This heterocyclic aromatic derivative has garnered attention due to its versatile applications and structural properties that make it a valuable intermediate in synthetic chemistry and drug development.

The molecular structure of Phenol, 2-(2-oxazolyl)- consists of a phenolic ring linked to an oxazole moiety. This unique arrangement imparts distinct chemical reactivity and biological potential, making it a subject of extensive study in both academic and industrial settings. The oxazole ring, characterized by its five-membered nitrogen-containing heterocycle, plays a crucial role in modulating the compound's interactions with biological targets.

In recent years, Phenol, 2-(2-oxazolyl)- has been explored for its potential in pharmaceutical applications. Its ability to act as a scaffold for drug design has led to the development of novel therapeutic agents targeting various diseases. For instance, studies have demonstrated its utility in creating compounds with anti-inflammatory and antimicrobial properties. The oxazole moiety, in particular, has been shown to enhance binding affinity to biological receptors, making it an attractive component in medicinal chemistry.

The synthesis of Phenol, 2-(2-oxazolyl)- involves multi-step organic reactions that highlight the compound's synthetic versatility. Researchers have developed efficient methodologies for its preparation, often utilizing palladium-catalyzed cross-coupling reactions to construct the oxazole-phenol linkage. These advances in synthetic chemistry have not only improved the accessibility of the compound but also paved the way for its incorporation into more complex molecular architectures.

One of the most compelling aspects of Phenol, 2-(2-oxazolyl)- is its role in developing bioactive molecules. The phenolic hydroxyl group provides a site for further functionalization, allowing chemists to tailor the compound's properties for specific applications. Additionally, the oxazole ring can participate in hydrogen bonding interactions, which is crucial for designing molecules with high selectivity and potency.

The pharmacological profile of derivatives of Phenol, 2-(2-oxazolyl)- has been extensively studied. Preclinical trials have shown promising results in several therapeutic areas, including oncology and neurodegenerative diseases. The compound's ability to modulate enzyme activity and receptor binding has opened new avenues for drug discovery. Researchers are particularly interested in its potential as an inhibitor of kinases and other enzymes implicated in disease pathogenesis.

The chemical stability of Phenol, 2-(2-oxazolyl)- under various conditions is another area of interest. Studies have investigated its behavior in different solvents and at varying temperatures to understand how these factors influence its reactivity and biological activity. Such knowledge is essential for optimizing its use in pharmaceutical formulations and ensuring its efficacy in real-world applications.

In conclusion, Phenol, 2-(2-oxazolyl)- (CAS No. 109604-76-4) represents a fascinating compound with broad applications in chemical synthesis and pharmaceutical research. Its unique structural features and functional properties make it a valuable tool for developing novel therapeutic agents. As research continues to uncover new aspects of this compound, its significance in advancing medical science is likely to grow even further.

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