Cas no 70502-03-3 (4-Oxazolemethanol,5-methyl-2-phenyl-)

4-Oxazolemethanol,5-methyl-2-phenyl- is a heterocyclic organic compound featuring an oxazole core substituted with a phenyl group at the 2-position and a hydroxymethyl group at the 4-position, along with a methyl group at the 5-position. This structure makes it a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its oxazole moiety is known for contributing to bioactive properties, while the hydroxymethyl group enhances reactivity for further functionalization. The compound’s stability and well-defined reactivity profile make it suitable for use in medicinal chemistry research, where precise molecular modifications are required. It is typically handled under controlled conditions due to its sensitivity.
4-Oxazolemethanol,5-methyl-2-phenyl- structure
70502-03-3 structure
Product Name:4-Oxazolemethanol,5-methyl-2-phenyl-
CAS No:70502-03-3
MF:C11H11NO2
MW:189.210542917252
MDL:MFCD08271881
CID:561976
Update Time:2025-10-05

4-Oxazolemethanol,5-methyl-2-phenyl- Chemical and Physical Properties

Names and Identifiers

    • 4-Oxazolemethanol,5-methyl-2-phenyl-
    • (5-methyl-2-phenyl-1,3-oxazol-4-yl)methanol
    • (5-methyl-2-phenyl-4-oxazolyl)methanol
    • (5-methyl-2-phenyloxazol-4-yl)methanol
    • [5-methyl-2-phenyl-1,3-oxazol-4-yl]methanol
    • 5-methyl-2-phenyl-4-hydroxymethyloxazole
    • 5-methyl-2-phenyl-4-oxazolemethanol
    • 5-Methyl-2-phenyloxazole-4-methanol
    • MDL： MFCD08271881
    • Inchi： 1S/C11H11NO2/c1-8-10(7-13)12-11(14-8)9-5-3-2-4-6-9/h2-6,13H,7H2,1H3
    • InChI Key： AAQIALLSQXGHHT-UHFFFAOYSA-N
    • SMILES： O1C(C2C=CC=CC=2)=NC(CO)=C1C

Computed Properties

  • Exact Mass: 189.07900

Experimental Properties

  • Density: 1.176
  • Melting Point: 117 °C
  • Boiling Point: 361.125°C at 760 mmHg
  • Flash Point: 172.202°C
  • Refractive Index: 1.567
  • PSA: 46.26000
  • LogP: 2.14230

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4-Oxazolemethanol,5-methyl-2-phenyl- Related Literature

Additional information on 4-Oxazolemethanol,5-methyl-2-phenyl-

Comprehensive Overview of 4-Oxazolemethanol,5-methyl-2-phenyl- (CAS No. 70502-03-3)

The compound 4-Oxazolemethanol,5-methyl-2-phenyl- (CAS No. 70502-03-3) is a specialized organic molecule featuring an oxazole core structure substituted with a phenyl group and a methyl group. This unique arrangement grants it distinct chemical properties, making it a subject of interest in pharmaceutical research, material science, and synthetic chemistry. The presence of both hydroxymethyl and aromatic functionalities enhances its versatility as a building block for more complex molecules.

In recent years, the demand for heterocyclic compounds like 4-Oxazolemethanol,5-methyl-2-phenyl- has surged due to their applications in drug discovery and agrochemical formulations. Researchers are particularly intrigued by its potential as a precursor for bioactive molecules, given the oxazole ring's prevalence in natural products and FDA-approved drugs. Its CAS No. 70502-03-3 serves as a critical identifier for regulatory and commercial purposes, ensuring precise tracking in global chemical databases.

The synthesis of 5-methyl-2-phenyl-4-oxazolemethanol typically involves multi-step organic reactions, including cyclization and functional group transformations. Advanced techniques such as microwave-assisted synthesis and catalyzed cross-coupling have been explored to improve yield and purity. These innovations align with the growing emphasis on green chemistry and sustainable practices, addressing concerns about waste reduction and energy efficiency in chemical manufacturing.

From an industrial perspective, CAS 70502-03-3 is often sourced for high-value intermediates in specialty chemicals. Its structural motifs are leveraged in designing fluorescent dyes, ligands for catalysis, and even polymeric materials with tailored properties. The compound's stability under varying pH conditions further broadens its utility in formulation science, a topic frequently queried in SEO searches related to "stable heterocyclic additives."

Analytical characterization of 4-Oxazolemethanol,5-methyl-2-phenyl- relies on techniques like NMR spectroscopy, mass spectrometry, and HPLC. These methods confirm its molecular identity and purity, which are critical for compliance with REACH and other regulatory frameworks. Discussions on platforms like ResearchGate often highlight challenges in isolating this compound, reflecting its niche yet growing relevance in academic and industrial labs.

Emerging trends also link oxazole derivatives to cancer research and antimicrobial agents, fueling interest in 70502-03-3 as a scaffold for novel therapeutics. Patent filings reveal its incorporation into kinase inhibitors and anti-inflammatory drugs, aligning with the rise of personalized medicine. Such applications resonate with search queries like "oxazole-based drug leads 2024," underscoring its intersection with cutting-edge science.

In summary, 4-Oxazolemethanol,5-methyl-2-phenyl- (CAS No. 70502-03-3) exemplifies the convergence of synthetic elegance and practical utility. Its role in advancing material innovation and life sciences ensures sustained attention from researchers and industries alike, while its optimized synthesis routes cater to the evolving demands of sustainable chemistry.

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