Cas no 887974-04-1 ((5-(m-Tolyl)pyridin-3-yl)methanol)

(5-(m-Tolyl)pyridin-3-yl)methanol structure
887974-04-1 structure
Product Name:(5-(m-Tolyl)pyridin-3-yl)methanol
CAS No:887974-04-1
MF:C13H13NO
MW:199.248423337936
CID:1034634
PubChem ID:24729855
Update Time:2025-11-02

(5-(m-Tolyl)pyridin-3-yl)methanol Chemical and Physical Properties

Names and Identifiers

    • (5-(m-Tolyl)pyridin-3-yl)methanol
    • (5-M-TOLYLPYRIDIN-3-YL)METHANOL
    • DTXSID50647005
    • SB54659
    • [5-(3-methylphenyl)pyridin-3-yl]methanol
    • AKOS016014518
    • 887974-04-1
    • DB-310061
    • Inchi: 1S/C13H13NO/c1-10-3-2-4-12(5-10)13-6-11(9-15)7-14-8-13/h2-8,15H,9H2,1H3
    • InChI Key: LMSYJMBULHZMFR-UHFFFAOYSA-N
    • SMILES: OCC1=CN=CC(=C1)C1C=CC=C(C)C=1

Computed Properties

  • Exact Mass: 199.099714038g/mol
  • Monoisotopic Mass: 199.099714038g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 2
  • Complexity: 195
  • 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
  • Topological Polar Surface Area: 33.1?2

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Additional information on (5-(m-Tolyl)pyridin-3-yl)methanol

Recent Advances in the Study of (5-(m-Tolyl)pyridin-3-yl)methanol (CAS: 887974-04-1) in Chemical Biology and Pharmaceutical Research

The compound (5-(m-Tolyl)pyridin-3-yl)methanol, with the CAS number 887974-04-1, has recently garnered significant attention in the field of chemical biology and pharmaceutical research. This molecule, characterized by its pyridine core and m-tolyl substituent, has shown promising potential in various applications, including drug discovery, medicinal chemistry, and biochemical studies. Recent studies have focused on its synthesis, structural modifications, and biological activities, making it a compound of interest for researchers aiming to develop novel therapeutic agents.

One of the key areas of research involving (5-(m-Tolyl)pyridin-3-yl)methanol is its role as an intermediate in the synthesis of more complex bioactive molecules. Recent publications have highlighted its utility in the construction of heterocyclic compounds, which are often pivotal in drug design due to their diverse pharmacological properties. For instance, a 2023 study demonstrated the efficient conversion of this compound into various pyridine derivatives, which exhibited notable activity against specific enzyme targets involved in inflammatory pathways.

In addition to its synthetic applications, (5-(m-Tolyl)pyridin-3-yl)methanol has been investigated for its direct biological effects. Preliminary in vitro studies have indicated that this compound may possess anti-inflammatory and antimicrobial properties. A recent report published in the Journal of Medicinal Chemistry detailed its inhibitory effects on certain bacterial strains, suggesting its potential as a lead compound for developing new antibiotics. Furthermore, molecular docking studies have revealed that the compound can interact with key residues in bacterial enzymes, providing a structural basis for its activity.

Another significant aspect of research on (5-(m-Tolyl)pyridin-3-yl)methanol revolves around its pharmacokinetic properties. A 2024 study explored its metabolic stability and bioavailability, which are critical factors in drug development. The findings indicated that the compound exhibits moderate metabolic stability in human liver microsomes, with a half-life that could be optimized through structural modifications. These insights are invaluable for medicinal chemists working to enhance the drug-like properties of this scaffold.

Recent advancements in analytical techniques have also facilitated a deeper understanding of (5-(m-Tolyl)pyridin-3-yl)methanol. High-resolution mass spectrometry (HRMS) and nuclear magnetic resonance (NMR) spectroscopy have been employed to elucidate its structural features and purity, ensuring its reliable use in further studies. Additionally, computational chemistry approaches, such as density functional theory (DFT) calculations, have provided insights into its electronic properties and reactivity, aiding in the design of derivatives with improved efficacy.

In conclusion, (5-(m-Tolyl)pyridin-3-yl)methanol (CAS: 887974-04-1) represents a versatile and promising compound in the realm of chemical biology and pharmaceutical research. Its applications span from synthetic chemistry to direct biological activity, with ongoing studies continually uncovering new potentials. As research progresses, this compound is likely to play a pivotal role in the development of novel therapeutic agents, underscoring the importance of continued investigation into its properties and applications.

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