Cas no 1261909-03-8 (5-(4-Methylphenyl)pyridin-3-ol)

5-(4-Methylphenyl)pyridin-3-ol is a heterocyclic compound featuring a pyridine core substituted with a hydroxyl group at the 3-position and a 4-methylphenyl moiety at the 5-position. This structure imparts unique electronic and steric properties, making it a valuable intermediate in pharmaceutical and agrochemical synthesis. The hydroxyl group enhances reactivity for further functionalization, while the methylphenyl substituent contributes to lipophilicity, influencing solubility and binding interactions. Its well-defined molecular architecture ensures consistency in synthetic applications, particularly in the development of bioactive molecules. The compound is characterized by high purity and stability, making it suitable for research and industrial-scale processes requiring precise chemical modifications.
5-(4-Methylphenyl)pyridin-3-ol structure
1261909-03-8 structure
Product Name:5-(4-Methylphenyl)pyridin-3-ol
CAS No:1261909-03-8
MF:C12H11NO
MW:185.221843004227
MDL:MFCD18311929
CID:2762781
PubChem ID:53217484
Update Time:2025-05-23

5-(4-Methylphenyl)pyridin-3-ol Chemical and Physical Properties

Names and Identifiers

    • 1261909-03-8
    • MFCD18311929
    • 3-Hydroxy-5-(4-tolyl)pyridine
    • A1-29718
    • DTXSID10682518
    • 3-HYDROXY-5-(4-METHYLPHENYL)PYRIDINE
    • 5-(p-Tolyl)pyridin-3-ol
    • AKOS006318471
    • 5-(4-Methylphenyl)pyridin-3-ol
    • MDL: MFCD18311929
    • Inchi: 1S/C12H11NO/c1-9-2-4-10(5-3-9)11-6-12(14)8-13-7-11/h2-8,14H,1H3
    • InChI Key: OAEZJNQHWQOBMX-UHFFFAOYSA-N
    • SMILES: OC1=CN=CC(=C1)C1C=CC(C)=CC=1

Computed Properties

  • Exact Mass: 185.084063974Da
  • Monoisotopic Mass: 185.084063974Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 1
  • Complexity: 175
  • 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: 2.5
  • Topological Polar Surface Area: 33.1?2

5-(4-Methylphenyl)pyridin-3-ol Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Matrix Scientific
218686-2.500g
5-(p-Tolyl)pyridin-3-ol, 95%
1261909-03-8 95%
2.500g
$1733.00 2023-09-06
A2B Chem LLC
AI19775-2.5g
3-Hydroxy-5-(4-tolyl)pyridine
1261909-03-8 95%
2.5g
$1151.00 2024-04-20

Additional information on 5-(4-Methylphenyl)pyridin-3-ol

Introduction to 5-(4-Methylphenyl)pyridin-3-ol and Its Significance in Modern Chemical Research

5-(4-Methylphenyl)pyridin-3-ol, a compound with the CAS number 1261909-03-8, represents a fascinating subject of study in the realm of chemical and pharmaceutical research. This compound, characterized by its unique structural features, has garnered attention due to its potential applications in various scientific domains. The molecular structure of 5-(4-Methylphenyl)pyridin-3-ol comprises a pyridine ring substituted with a 4-methylphenyl group at the 5-position and a hydroxyl group at the 3-position. This configuration imparts distinct chemical properties that make it a valuable candidate for further exploration.

The significance of 5-(4-Methylphenyl)pyridin-3-ol in contemporary research is underscored by its versatility and the potential it holds for developing novel therapeutic agents. The presence of both aromatic and heterocyclic components in its structure suggests that it may exhibit a range of biological activities. Recent studies have begun to uncover the pharmacological properties of this compound, indicating its potential as an intermediate in the synthesis of more complex molecules with therapeutic benefits.

In the context of drug discovery, the structural motif of 5-(4-Methylphenyl)pyridin-3-ol is particularly noteworthy. The pyridine ring is a common scaffold in many bioactive molecules, and its combination with a substituted benzene ring can enhance binding affinity to biological targets. This has led researchers to investigate its interactions with various enzymes and receptors, aiming to identify new pharmacological pathways. The hydroxyl group at the 3-position further adds to its reactivity, making it a promising candidate for further functionalization.

The latest advancements in computational chemistry have also played a crucial role in understanding the behavior of 5-(4-Methylphenyl)pyridin-3-ol. Molecular modeling studies have provided insights into its binding modes with potential target proteins, which are essential for designing more effective derivatives. These simulations have helped researchers predict the compound's pharmacokinetic properties, such as solubility and metabolic stability, which are critical factors in drug development.

Beyond its pharmaceutical applications, 5-(4-Methylphenyl)pyridin-3-ol has shown promise in material science. Its unique electronic properties make it a candidate for use in organic semiconductors and other advanced materials. The ability to tune its properties through structural modifications opens up possibilities for innovative technological applications. This dual utility as both a pharmaceutical intermediate and a material component highlights the broad scope of research that can be conducted around this compound.

The synthesis of 5-(4-Methylphenyl)pyridin-3-ol is another area of active investigation. Researchers have developed several synthetic routes to produce this compound efficiently and in high yield. These methods often involve multi-step organic transformations, including condensation reactions, cyclization processes, and functional group modifications. Optimizing these synthetic pathways is crucial for ensuring that sufficient quantities of the compound can be produced for both research and commercial purposes.

In conclusion, 5-(4-Methylphenyl)pyridin-3-ol, with its CAS number 1261909-03-8, represents a multifaceted compound with significant implications in chemical research. Its unique structural features and potential applications in pharmaceuticals and materials science make it a subject of great interest. As research continues to uncover new aspects of this molecule, its importance is likely to grow, contributing to advancements across multiple scientific disciplines.

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