Cas no 1227515-71-0 (6-METHOXY-2-METHYLPYRIDINE-3-CARBOXYLIC ACID)

6-Methoxy-2-methylpyridine-3-carboxylic acid is a versatile heterocyclic compound featuring a pyridine core substituted with methoxy and methyl groups at the 6- and 2-positions, respectively, along with a carboxylic acid functionality at the 3-position. This structure makes it a valuable intermediate in pharmaceutical and agrochemical synthesis, particularly for constructing bioactive molecules. Its electron-rich aromatic system and reactive carboxyl group enable efficient derivatization, facilitating the development of targeted compounds. The methoxy and methyl substituents enhance steric and electronic properties, influencing reactivity and selectivity in coupling reactions. Suitable for use in medicinal chemistry and material science, it offers a balance of stability and reactivity for diverse synthetic applications.
6-METHOXY-2-METHYLPYRIDINE-3-CARBOXYLIC ACID structure
1227515-71-0 structure
Product Name:6-METHOXY-2-METHYLPYRIDINE-3-CARBOXYLIC ACID
CAS No:1227515-71-0
MF:C8H9NO3
MW:167.161962270737
MDL:MFCD16611508
CID:2199749
PubChem ID:53395577
Update Time:2025-06-11

6-METHOXY-2-METHYLPYRIDINE-3-CARBOXYLIC ACID Chemical and Physical Properties

Names and Identifiers

    • 6-METHOXY-2-METHYLPYRIDINE-3-CARBOXYLIC ACID
    • SB21277
    • W-205151
    • Z1255389271
    • 1227515-71-0
    • AKOS017516119
    • J-518841
    • MFCD16611508
    • 6-Methoxy-2-methylnicotinic acid
    • DTXSID10694171
    • 3-Pyridinecarboxylic acid, 6-methoxy-2-methyl-
    • 6-Methoxy-2-methylnicotinicacid
    • SCHEMBL838850
    • CS-0183609
    • EN300-7418618
    • BS-19511
    • DB-140788
    • MDL: MFCD16611508
    • Inchi: 1S/C8H9NO3/c1-5-6(8(10)11)3-4-7(9-5)12-2/h3-4H,1-2H3,(H,10,11)
    • InChI Key: FVJDKDPPYPBOEP-UHFFFAOYSA-N
    • SMILES: O(C)C1=CC=C(C(=O)O)C(C)=N1

Computed Properties

  • Exact Mass: 167.058243149g/mol
  • Monoisotopic Mass: 167.058243149g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 2
  • Complexity: 172
  • 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: 1.1
  • Topological Polar Surface Area: 59.4?2

6-METHOXY-2-METHYLPYRIDINE-3-CARBOXYLIC ACID Pricemore >>

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Additional information on 6-METHOXY-2-METHYLPYRIDINE-3-CARBOXYLIC ACID

Research Briefing on 6-METHOXY-2-METHYLPYRIDINE-3-CARBOXYLIC ACID (CAS: 1227515-71-0) and Its Applications in Chemical Biology and Pharmaceutical Research

6-METHOXY-2-METHYLPYRIDINE-3-CARBOXYLIC ACID (CAS: 1227515-71-0) is a pyridine derivative that has garnered significant attention in recent years due to its potential applications in chemical biology and pharmaceutical research. This compound serves as a key intermediate in the synthesis of various bioactive molecules, including kinase inhibitors and other therapeutic agents. Recent studies have explored its utility in drug discovery, particularly in the development of targeted therapies for cancer and inflammatory diseases.

One of the most notable applications of 6-METHOXY-2-METHYLPYRIDINE-3-CARBOXYLIC ACID is its role as a building block for the synthesis of small-molecule inhibitors. For instance, it has been used in the development of compounds targeting the JAK-STAT signaling pathway, which is implicated in numerous autoimmune and inflammatory conditions. Researchers have demonstrated that derivatives of this compound exhibit potent inhibitory activity against JAK kinases, making them promising candidates for further preclinical evaluation.

In addition to its role in kinase inhibitor development, 6-METHOXY-2-METHYLPYRIDINE-3-CARBOXYLIC ACID has also been investigated for its potential in medicinal chemistry. Recent publications highlight its use in the design of novel prodrugs and drug delivery systems. For example, its carboxylic acid moiety allows for facile conjugation with other pharmacophores, enabling the creation of hybrid molecules with enhanced bioavailability and target specificity. This versatility underscores its value as a scaffold in drug design.

Recent advancements in synthetic methodologies have further expanded the utility of 6-METHOXY-2-METHYLPYRIDINE-3-CARBOXYLIC ACID. A 2023 study published in the Journal of Medicinal Chemistry described a streamlined, high-yield synthesis route for this compound, which significantly reduces production costs and improves scalability. This development is particularly relevant for industrial applications, where cost-effective synthesis of intermediates is critical for large-scale drug manufacturing.

Beyond its pharmaceutical applications, 6-METHOXY-2-METHYLPYRIDINE-3-CARBOXYLIC ACID has also been explored in chemical biology as a tool for probing enzyme mechanisms. Its structural features make it a suitable substrate for studying the activity of carboxylate-processing enzymes, such as decarboxylases and esterases. Researchers have utilized this compound to gain insights into enzyme-substrate interactions, paving the way for the design of more effective enzyme inhibitors.

In conclusion, 6-METHOXY-2-METHYLPYRIDINE-3-CARBOXYLIC ACID (CAS: 1227515-71-0) represents a versatile and valuable compound in the fields of chemical biology and pharmaceutical research. Its applications range from drug discovery and medicinal chemistry to enzyme mechanism studies, highlighting its broad utility. Ongoing research continues to uncover new opportunities for this compound, reinforcing its importance as a key intermediate in the development of next-generation therapeutics.

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