Cas no 1093879-95-8 ((6-chloro-2-methylpyridin-3-yl)methanol)

(6-Chloro-2-methylpyridin-3-yl)methanol is a versatile pyridine derivative with a hydroxymethyl functional group at the 3-position and chloro and methyl substituents at the 6- and 2-positions, respectively. This compound serves as a valuable intermediate in pharmaceutical and agrochemical synthesis, particularly in the development of active ingredients and fine chemicals. Its reactive hydroxymethyl group enables further functionalization, while the chloro substituent enhances its utility in cross-coupling reactions. The structural features of this compound contribute to its stability and compatibility with a range of reaction conditions, making it a practical choice for researchers in medicinal chemistry and material science. High purity grades are typically available to ensure consistent performance in synthetic applications.
(6-chloro-2-methylpyridin-3-yl)methanol structure
1093879-95-8 structure
Product Name:(6-chloro-2-methylpyridin-3-yl)methanol
CAS No:1093879-95-8
MF:C7H8ClNO
MW:157.597520828247
MDL:MFCD13689158
CID:1098579
PubChem ID:59525984
Update Time:2025-11-02

(6-chloro-2-methylpyridin-3-yl)methanol Chemical and Physical Properties

Names and Identifiers

    • 6-chloro-2-methyl-3-Pyridinemethanol
    • (6-Chloro-2-methyl-3-pyridinyl)methanol
    • (6-chloro-2-methylpyridin-3-yl)methanol
    • CTCQLOYWGIDQDZ-UHFFFAOYSA-N
    • 1093879-95-8
    • AS-47903
    • DA-15658
    • EN300-119026
    • AKOS026727300
    • F16741
    • AB88105
    • SCHEMBL3509762
    • Z1255459281
    • MFCD13689158
    • CS-0193928
    • MDL: MFCD13689158
    • Inchi: 1S/C7H8ClNO/c1-5-6(4-10)2-3-7(8)9-5/h2-3,10H,4H2,1H3
    • InChI Key: CTCQLOYWGIDQDZ-UHFFFAOYSA-N
    • SMILES: ClC1=CC=C(CO)C(C)=N1

Computed Properties

  • Exact Mass: 157.0294416g/mol
  • Monoisotopic Mass: 157.0294416g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 1
  • Complexity: 110
  • 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: 1.3
  • Topological Polar Surface Area: 33.1?2

(6-chloro-2-methylpyridin-3-yl)methanol Pricemore >>

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Additional information on (6-chloro-2-methylpyridin-3-yl)methanol

Comprehensive Guide to (6-chloro-2-methylpyridin-3-yl)methanol (CAS No. 1093879-95-8): Properties, Applications, and Market Insights

(6-chloro-2-methylpyridin-3-yl)methanol (CAS No. 1093879-95-8) is a specialized pyridine derivative with significant relevance in pharmaceutical and agrochemical research. This compound, characterized by its chloro-methylpyridine structure, serves as a key intermediate in the synthesis of various bioactive molecules. Its unique chemical properties make it valuable for drug discovery and material science applications.

The molecular structure of (6-chloro-2-methylpyridin-3-yl)methanol features a hydroxymethyl group at the 3-position and a chlorine substituent at the 6-position of the pyridine ring. This specific arrangement contributes to its reactivity and makes it particularly useful in cross-coupling reactions and heterocyclic chemistry. Researchers often search for "1093879-95-8 synthesis method" or "6-chloro-2-methylpyridin-3-yl methanol applications" when exploring its potential uses.

In pharmaceutical applications, (6-chloro-2-methylpyridin-3-yl)methanol has gained attention for its role in developing kinase inhibitors and central nervous system (CNS) drugs. Recent studies highlight its potential in addressing neurological disorders, a hot topic in medical research. The compound's ability to serve as a building block for small molecule therapeutics makes it particularly valuable in drug discovery pipelines.

The agrochemical industry utilizes 6-chloro-2-methylpyridin-3-yl methanol derivatives in developing novel pesticides and herbicides. With increasing global focus on sustainable agriculture, researchers are investigating how modifications of this compound can lead to more environmentally friendly crop protection solutions. Common search queries like "CAS 1093879-95-8 in agrochemicals" reflect this growing interest.

From a chemical perspective, (6-chloro-2-methylpyridin-3-yl)methanol demonstrates interesting solubility properties and thermal stability, making it suitable for various synthetic processes. Its melting point and boiling point characteristics are frequently searched parameters, as they determine processing conditions in industrial applications.

The market for pyridine derivatives like 1093879-95-8 has seen steady growth, driven by demand from the pharmaceutical sector. Recent market analyses show increased interest in "custom synthesis of (6-chloro-2-methylpyridin-3-yl)methanol" as companies seek specialized intermediates for drug development programs.

Quality control of (6-chloro-2-methylpyridin-3-yl)methanol typically involves HPLC analysis and spectroscopic characterization. Purity standards are crucial, especially when the compound is used in pharmaceutical applications. Analytical methods for this compound are frequently discussed in research forums and technical publications.

Environmental considerations for 6-chloro-2-methylpyridin-3-yl methanol production and handling have become increasingly important. The industry is moving toward greener synthesis methods, with researchers exploring catalytic processes and solvent-free reactions to minimize environmental impact.

Storage and handling recommendations for CAS 1093879-95-8 emphasize protection from moisture and extreme temperatures. Proper storage conditions ensure the compound's stability and maintain its reactivity for subsequent chemical transformations.

Future research directions for (6-chloro-2-methylpyridin-3-yl)methanol include exploring its potential in material science applications and developing more efficient synthetic routes. The compound's versatility continues to attract interest from multiple scientific disciplines.

For researchers working with 1093879-95-8, understanding its structure-activity relationships is crucial for designing effective derivatives. Computational chemistry approaches are increasingly being applied to predict the behavior of modified versions of this compound.

The global supply chain for (6-chloro-2-methylpyridin-3-yl)methanol has expanded in recent years, with specialized chemical manufacturers offering custom synthesis services. This availability supports ongoing research in medicinal chemistry and material development.

Patent analysis reveals growing intellectual property activity surrounding 6-chloro-2-methylpyridin-3-yl methanol derivatives, particularly in pharmaceutical applications. This trend indicates the compound's importance in developing new therapeutic agents.

In conclusion, (6-chloro-2-methylpyridin-3-yl)methanol (CAS No. 1093879-95-8) represents a valuable chemical building block with diverse applications across multiple industries. Its continued study promises to yield important advancements in drug discovery, agricultural science, and material development.

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