Cas no 1881320-69-9 (6-Chloro-5-methoxypyridine-3-carboxamide)

6-Chloro-5-methoxypyridine-3-carboxamide is a heterocyclic organic compound featuring a pyridine core substituted with chloro, methoxy, and carboxamide functional groups. This structure imparts versatility in synthetic applications, particularly in pharmaceutical and agrochemical research. The chloro and methoxy groups enhance reactivity, enabling selective modifications, while the carboxamide moiety offers hydrogen-bonding potential for interactions in biological systems. Its well-defined molecular framework makes it a valuable intermediate in the development of active ingredients, including kinase inhibitors and other bioactive molecules. The compound's stability and purity are critical for reproducible results in medicinal chemistry and material science applications.
6-Chloro-5-methoxypyridine-3-carboxamide structure
1881320-69-9 structure
Product Name:6-Chloro-5-methoxypyridine-3-carboxamide
CAS No:1881320-69-9
MF:C7H7ClN2O2
MW:186.595680475235
MDL:MFCD28657055
CID:4709406
PubChem ID:91729974
Update Time:2025-05-22

6-Chloro-5-methoxypyridine-3-carboxamide Chemical and Physical Properties

Names and Identifiers

    • 6-Chloro-5-methoxynicotinamide
    • 6-chloro-5-methoxypyridine-3-carboxamide
    • GEDDULRRCOXEQD-UHFFFAOYSA-N
    • FCH4139782
    • 3-pyridinecarboxamide, 6-chloro-5-methoxy-
    • AX8330451
    • MFCD28657055
    • SB53067
    • D79886
    • 1881320-69-9
    • CS-0449055
    • 6-Chloro-5-methoxypyridine-3-carboxamide
    • MDL: MFCD28657055
    • Inchi: 1S/C7H7ClN2O2/c1-12-5-2-4(7(9)11)3-10-6(5)8/h2-3H,1H3,(H2,9,11)
    • InChI Key: GEDDULRRCOXEQD-UHFFFAOYSA-N
    • SMILES: ClC1=C(C=C(C(N)=O)C=N1)OC

Computed Properties

  • Exact Mass: 186.0196052g/mol
  • Monoisotopic Mass: 186.0196052g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 2
  • Complexity: 177
  • 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
  • Topological Polar Surface Area: 65.2
  • XLogP3: 0.7

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Additional information on 6-Chloro-5-methoxypyridine-3-carboxamide

Recent Advances in the Study of 6-Chloro-5-methoxypyridine-3-carboxamide (CAS: 1881320-69-9)

6-Chloro-5-methoxypyridine-3-carboxamide (CAS: 1881320-69-9) is a chemical compound of significant interest in the field of chemical biology and pharmaceutical research. Recent studies have highlighted its potential as a key intermediate in the synthesis of novel therapeutic agents, particularly in the development of kinase inhibitors and other small-molecule drugs. This research brief aims to summarize the latest findings related to this compound, focusing on its chemical properties, biological activities, and potential applications in drug discovery.

The compound's unique structural features, including the chloro and methoxy substituents on the pyridine ring, contribute to its reactivity and binding affinity with various biological targets. Recent synthetic methodologies have optimized the production of 6-Chloro-5-methoxypyridine-3-carboxamide, enabling its broader use in medicinal chemistry. Notably, its role as a precursor in the synthesis of kinase inhibitors has been extensively investigated, with promising results in preclinical models of cancer and inflammatory diseases.

In a 2023 study published in the Journal of Medicinal Chemistry, researchers demonstrated the efficacy of derivatives of 6-Chloro-5-methoxypyridine-3-carboxamide in selectively inhibiting specific kinases involved in tumor proliferation. The study utilized structure-activity relationship (SAR) analysis to identify key modifications that enhance both potency and selectivity. These findings underscore the compound's versatility as a scaffold for drug development.

Another area of active research involves the compound's potential applications in neurodegenerative diseases. A recent preprint on bioRxiv reported that 6-Chloro-5-methoxypyridine-3-carboxamide derivatives exhibit neuroprotective effects in vitro, possibly through modulation of oxidative stress pathways. While further validation is required, these preliminary results suggest a promising avenue for future therapeutic development.

From a chemical perspective, advances in the characterization of 6-Chloro-5-methoxypyridine-3-carboxamide have been facilitated by improved analytical techniques, such as high-resolution mass spectrometry (HRMS) and nuclear magnetic resonance (NMR) spectroscopy. These tools have enabled researchers to elucidate the compound's stability, solubility, and degradation profiles, which are critical for its formulation in drug products.

In conclusion, 6-Chloro-5-methoxypyridine-3-carboxamide (CAS: 1881320-69-9) represents a valuable building block in modern drug discovery. Its diverse applications, ranging from oncology to neurology, highlight its importance in the chemical biology and pharmaceutical industries. Ongoing research is expected to further expand its utility, particularly in the design of next-generation therapeutics with improved efficacy and safety profiles.

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