Cas no 101257-87-8 (4-methylpyrimidin-5-ol)

4-Methylpyrimidin-5-ol is a heterocyclic organic compound featuring a pyrimidine core substituted with a methyl group at the 4-position and a hydroxyl group at the 5-position. This structure imparts unique reactivity, making it a valuable intermediate in pharmaceutical and agrochemical synthesis. Its pyrimidine scaffold is particularly significant in the development of nucleoside analogs and enzyme inhibitors. The compound’s functional groups allow for further derivatization, enabling tailored modifications for specific applications. High purity grades are available to ensure consistency in research and industrial processes. Its stability and well-characterized properties make it a reliable choice for synthetic chemistry applications.
4-methylpyrimidin-5-ol structure
4-methylpyrimidin-5-ol structure
Product Name:4-methylpyrimidin-5-ol
CAS No:101257-87-8
MF:C5H6N2O
MW:110.11394071579
CID:124575
PubChem ID:14341511
Update Time:2025-06-14

4-methylpyrimidin-5-ol Chemical and Physical Properties

Names and Identifiers

    • 5-Pyrimidinol,4-methyl-
    • 4-methylpyrimidin-5-ol
    • 5-Hydroxy-4-methylpyrimidine
    • 4-Methyl-5-hydroxypyrimidine
    • 4-methyl-pyrimidin-5-ol
    • 5-Pyrimidinol,4-methyl
    • 5-Pyrimidinol, 4-methyl- (6CI,9CI)
    • AKOS006275538
    • SCHEMBL1760847
    • E82635
    • SB56459
    • EN300-1859595
    • 5-Pyrimidinol, 4-methyl-
    • CS-0310898
    • 101257-87-8
    • DTXSID70559116
    • FT-0716451
    • DB-081951
    • Inchi: 1S/C5H6N2O/c1-4-5(8)2-6-3-7-4/h2-3,8H,1H3
    • InChI Key: WPXHBJUNZGWFJD-UHFFFAOYSA-N
    • SMILES: OC1=CN=CN=C1C

Computed Properties

  • Exact Mass: 110.04800
  • Monoisotopic Mass: 110.048012819g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 8
  • Rotatable Bond Count: 0
  • Complexity: 76.8
  • 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: 0.2
  • Topological Polar Surface Area: 46?2

Experimental Properties

  • Density: 1.216
  • Boiling Point: 229.748 °C at 760 mmHg
  • Flash Point: 92.748 °C
  • PSA: 46.01000
  • LogP: 0.49060

4-methylpyrimidin-5-ol Pricemore >>

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Additional information on 4-methylpyrimidin-5-ol

Comprehensive Overview of 4-methylpyrimidin-5-ol (CAS No. 101257-87-8): Properties, Applications, and Industry Trends

4-methylpyrimidin-5-ol (CAS No. 101257-87-8) is a heterocyclic organic compound with a pyrimidine backbone, widely recognized for its versatile applications in pharmaceuticals, agrochemicals, and material science. The compound's molecular structure, featuring a hydroxyl group at the 5-position and a methyl group at the 4-position of the pyrimidine ring, contributes to its unique reactivity and functional utility. Researchers and industries increasingly focus on 4-methylpyrimidin-5-ol derivatives due to their potential in drug discovery and sustainable chemistry.

In recent years, the demand for pyrimidine-based compounds has surged, driven by their role in developing kinase inhibitors and antiviral agents. 4-methylpyrimidin-5-ol serves as a key intermediate in synthesizing bioactive molecules, aligning with the growing interest in targeted drug delivery systems and green synthesis methods. Its compatibility with microwave-assisted and enzymatic reactions makes it a candidate for eco-friendly production processes, addressing the industry's shift toward sustainable chemical manufacturing.

The compound's physicochemical properties, including solubility in polar solvents and thermal stability, have been extensively studied. Analytical techniques such as HPLC, NMR, and mass spectrometry are commonly employed for purity assessment, reflecting the stringent quality standards required in pharmaceutical intermediates. Users searching for "CAS 101257-87-8 supplier" or "4-methylpyrimidin-5-ol synthesis protocol" often seek data on scalable production routes, which underscores the need for detailed technical literature.

Emerging applications of 4-methylpyrimidin-5-ol in organic electronics and catalysis further highlight its interdisciplinary relevance. For instance, its incorporation into metal-organic frameworks (MOFs) has been explored for gas storage, resonating with trends in clean energy solutions. Additionally, the compound's role in photocatalysis aligns with searches for "visible-light-driven reactions"—a hot topic in synthetic chemistry.

Regulatory and safety profiles of 4-methylpyrimidin-5-ol are frequently queried, particularly regarding REACH compliance and handling guidelines. While the compound is not classified as hazardous under current regulations, proper storage conditions (e.g., inert atmosphere, low humidity) are recommended to maintain stability. This aligns with industry-wide emphasis on chemical safety best practices.

In conclusion, 4-methylpyrimidin-5-ol (CAS No. 101257-87-8) exemplifies the intersection of traditional heterocyclic chemistry and modern technological demands. Its adaptability across sectors—from medicinal chemistry to advanced materials—positions it as a compound of enduring significance. Future research may explore its potential in bioconjugation or nanotechnology, areas generating substantial academic and commercial interest.

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