Cas no 1196157-41-1 ([2-chloro-6-(trifluoromethyl)pyridin-4-yl]methanol)

[2-Chloro-6-(trifluoromethyl)pyridin-4-yl]methanol is a fluorinated pyridine derivative characterized by a chlorinated and trifluoromethyl-substituted aromatic ring with a hydroxymethyl functional group. This structure imparts unique reactivity, making it a valuable intermediate in pharmaceutical and agrochemical synthesis. The trifluoromethyl group enhances lipophilicity and metabolic stability, while the chlorinated pyridine core offers versatility in cross-coupling reactions. The hydroxymethyl moiety provides a handle for further functionalization, enabling derivatization into esters, ethers, or other targeted compounds. Its well-defined purity and stability under controlled conditions ensure consistent performance in synthetic applications. This compound is particularly useful in the development of bioactive molecules requiring fluorinated aromatic scaffolds.
[2-chloro-6-(trifluoromethyl)pyridin-4-yl]methanol structure
1196157-41-1 structure
Product Name:[2-chloro-6-(trifluoromethyl)pyridin-4-yl]methanol
CAS No:1196157-41-1
MF:C7H5ClF3NO
MW:211.568911314011
MDL:MFCD13190043
CID:4457110
PubChem ID:72212583
Update Time:2025-10-29

[2-chloro-6-(trifluoromethyl)pyridin-4-yl]methanol Chemical and Physical Properties

Names and Identifiers

    • [2-chloro-6-(trifluoromethyl)pyridin-4-yl]methanol
    • 2-Chloro-6-(trifluoroMethyl)-4-pyridineMethanol
    • (2-CHLORO-6-TRIFLUOROMETHYL-PYRIDIN-4-YL)-METHANOL
    • 2-Chloro-6-(trifluoromethyl)pyridine-4-methanol
    • 4-Pyridinemethanol, 2-chloro-6-(trifluoromethyl)-
    • (2-CHLORO-6-(TRIFLUOROMETHYL)PYRIDIN-4-YL)METHANOL
    • 1196157-41-1
    • AKOS027321931
    • CS-0194184
    • EN300-746331
    • F13417
    • [2-Chloro-6-(trifluoromethyl)-4-pyridyl]methanol
    • SCHEMBL6120892
    • DB-093737
    • AB69640
    • DTXSID101241793
    • MFCD13190043
    • DTXCID001672680
    • 833-701-2
    • WXB15741
    • MDL: MFCD13190043
    • Inchi: 1S/C7H5ClF3NO/c8-6-2-4(3-13)1-5(12-6)7(9,10)11/h1-2,13H,3H2
    • InChI Key: ZFHFVKOYKPAGNL-UHFFFAOYSA-N
    • SMILES: ClC1=CC(CO)=CC(C(F)(F)F)=N1

Computed Properties

  • Exact Mass: 211.0011760g/mol
  • Monoisotopic Mass: 211.0011760g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 2
  • Complexity: 176
  • 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: 1.8
  • Topological Polar Surface Area: 33.1?2

[2-chloro-6-(trifluoromethyl)pyridin-4-yl]methanol Pricemore >>

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Additional information on [2-chloro-6-(trifluoromethyl)pyridin-4-yl]methanol

Comprehensive Overview of [2-chloro-6-(trifluoromethyl)pyridin-4-yl]methanol (CAS No. 1196157-41-1)

The compound [2-chloro-6-(trifluoromethyl)pyridin-4-yl]methanol (CAS No. 1196157-41-1) is a specialized pyridine derivative with significant applications in pharmaceutical intermediates and agrochemical synthesis. Its unique structure, featuring a chloro and trifluoromethyl substitution on the pyridine ring, along with a hydroxymethyl functional group, makes it a versatile building block in modern organic chemistry. Researchers and industries are increasingly interested in this compound due to its potential in drug discovery and crop protection formulations.

One of the most searched questions related to [2-chloro-6-(trifluoromethyl)pyridin-4-yl]methanol is its synthetic route and purity standards. The compound is typically synthesized through multistep organic reactions, involving halogenation and reduction processes. High-performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR) are commonly employed to verify its purity, which is critical for applications in precision chemistry. Recent advancements in green chemistry have also sparked interest in optimizing its synthesis to reduce environmental impact.

Another trending topic is the role of [2-chloro-6-(trifluoromethyl)pyridin-4-yl]methanol in bioactive molecule design. Its trifluoromethyl group enhances lipophilicity and metabolic stability, making it valuable for medicinal chemistry projects. For instance, it has been explored as a precursor in the development of kinase inhibitors and antimicrobial agents. The compound’s structure-activity relationship (SAR) is frequently studied to improve drug efficacy and selectivity.

In the agrochemical sector, [2-chloro-6-(trifluoromethyl)pyridin-4-yl]methanol is gaining attention for its potential in pesticide formulations. The chloro and trifluoromethyl moieties contribute to its pest resistance properties, aligning with the growing demand for sustainable crop solutions. Farmers and researchers often inquire about its mode of action and environmental degradation profile, which are key factors in regulatory approvals.

Storage and handling of CAS No. 1196157-41-1 are also frequently discussed. Proper storage conditions, such as cool, dry environments in airtight containers, are essential to maintain its stability. Safety data sheets (SDS) provide detailed guidelines to ensure safe laboratory practices. Additionally, the compound’s solubility in common organic solvents like dichloromethane and ethanol is a practical consideration for experimental workflows.

The future of [2-chloro-6-(trifluoromethyl)pyridin-4-yl]methanol lies in its adaptability to high-throughput screening and combinatorial chemistry. With the rise of artificial intelligence (AI) in chemical research, predictive models are being developed to explore its derivatives for novel applications. This aligns with the broader trend of digital transformation in the chemical industry, where computational chemistry tools accelerate discovery.

In summary, [2-chloro-6-(trifluoromethyl)pyridin-4-yl]methanol (CAS No. 1196157-41-1) is a multifaceted compound with expanding relevance in life sciences and material innovation. Its synthetic versatility, bioactivity, and industrial applicability make it a subject of ongoing research and commercial interest. As scientific inquiries evolve, this compound is poised to play a pivotal role in addressing global challenges in healthcare and agriculture.

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