Cas no 1214386-12-5 (Methyl 5-chloro-6-methoxypicolinate)

Methyl 5-chloro-6-methoxypicolinate is a versatile intermediate in organic synthesis, particularly valued for its role in pharmaceutical and agrochemical applications. Its picolinate structure, featuring both chloro and methoxy substituents, enhances reactivity in cross-coupling reactions and other transformations. The ester group provides a handle for further functionalization, making it useful in constructing complex heterocyclic frameworks. The compound’s stability under standard conditions ensures consistent performance in synthetic workflows. Its high purity and well-defined reactivity profile make it a reliable choice for researchers developing active ingredients or specialty chemicals. The balance of electron-withdrawing and electron-donating groups contributes to its utility in fine chemical synthesis.
Methyl 5-chloro-6-methoxypicolinate structure
1214386-12-5 structure
Product Name:Methyl 5-chloro-6-methoxypicolinate
CAS No:1214386-12-5
MF:C8H8ClNO3
MW:201.607021331787
CID:1095270
PubChem ID:46311247
Update Time:2025-10-29

Methyl 5-chloro-6-methoxypicolinate Chemical and Physical Properties

Names and Identifiers

    • Methyl 5-chloro-6-methoxypicolinate
    • methyl 5-chloro-6-methoxypyridine-2-carboxylate
    • 1214386-12-5
    • SCHEMBL16652958
    • Methyl5-chloro-6-methoxypicolinate
    • 2-Pyridinecarboxylic acid, 5-chloro-6-methoxy-, methyl ester
    • Inchi: 1S/C8H8ClNO3/c1-12-7-5(9)3-4-6(10-7)8(11)13-2/h3-4H,1-2H3
    • InChI Key: JHMGFCFCTFVGOS-UHFFFAOYSA-N
    • SMILES: ClC1C=CC(C(=O)OC)=NC=1OC

Computed Properties

  • Exact Mass: 201.0192708g/mol
  • Monoisotopic Mass: 201.0192708g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 3
  • Complexity: 188
  • 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: 48.4?2

Methyl 5-chloro-6-methoxypicolinate Pricemore >>

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Additional information on Methyl 5-chloro-6-methoxypicolinate

Recent Advances in the Application of Methyl 5-chloro-6-methoxypicolinate (CAS: 1214386-12-5) in Chemical Biology and Pharmaceutical Research

Methyl 5-chloro-6-methoxypicolinate (CAS: 1214386-12-5) has emerged as a key intermediate in the synthesis of biologically active compounds, particularly in the development of novel pharmaceuticals. Recent studies have highlighted its utility in the construction of heterocyclic scaffolds, which are pivotal in drug discovery. This compound's unique chemical properties, including its reactivity and stability under various conditions, make it an attractive candidate for further exploration in medicinal chemistry.

One of the most significant applications of Methyl 5-chloro-6-methoxypicolinate is in the synthesis of kinase inhibitors. Kinases play a crucial role in cellular signaling pathways, and their dysregulation is associated with numerous diseases, including cancer and inflammatory disorders. Researchers have utilized this compound to develop potent and selective inhibitors targeting specific kinases, demonstrating promising results in preclinical studies. The ability to modify the picolinate moiety allows for fine-tuning of the inhibitors' pharmacokinetic properties, enhancing their therapeutic potential.

In addition to its role in kinase inhibitor development, Methyl 5-chloro-6-methoxypicolinate has been employed in the synthesis of agrochemicals. Its structural features contribute to the efficacy of pesticides and herbicides, offering improved pest control and crop protection. Recent advancements in synthetic methodologies have enabled more efficient and scalable production of this compound, facilitating its broader application in both pharmaceutical and agricultural industries.

Recent publications have also explored the mechanistic insights into the reactivity of Methyl 5-chloro-6-methoxypicolinate. Detailed spectroscopic and computational studies have elucidated its behavior in various chemical transformations, providing a deeper understanding of its potential applications. These findings are instrumental in guiding the design of new derivatives with enhanced biological activity and reduced off-target effects.

Looking ahead, the continued investigation of Methyl 5-chloro-6-methoxypicolinate and its derivatives holds great promise for the discovery of next-generation therapeutics. Collaborative efforts between academic institutions and pharmaceutical companies are expected to accelerate the translation of these findings into clinical applications. The compound's versatility and the growing body of research supporting its use underscore its importance in the field of chemical biology and drug development.

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