Cas no 126798-27-4 (1,2-dihydro-3-methyl-2-oxo-4-Pyridinecarboxylic acid)

1,2-Dihydro-3-methyl-2-oxo-4-pyridinecarboxylic acid is a heterocyclic organic compound featuring a pyridine core with a carboxylic acid substituent at the 4-position and a methyl group at the 3-position. This structure imparts versatility in synthetic applications, particularly as an intermediate in pharmaceutical and agrochemical synthesis. The presence of both carboxylic acid and keto functionalities enhances its reactivity, enabling use in condensation, cyclization, and derivatization reactions. Its stable crystalline form ensures consistent handling and storage. The compound's well-defined molecular architecture makes it valuable for constructing complex heterocycles or modifying bioactive molecules, offering researchers a reliable building block for drug discovery and material science applications.
1,2-dihydro-3-methyl-2-oxo-4-Pyridinecarboxylic acid structure
126798-27-4 structure
Product Name:1,2-dihydro-3-methyl-2-oxo-4-Pyridinecarboxylic acid
CAS No:126798-27-4
MF:C7H7NO3
MW:153.135381937027
MDL:MFCD18803541
CID:103335
PubChem ID:23255449
Update Time:2025-08-04

1,2-dihydro-3-methyl-2-oxo-4-Pyridinecarboxylic acid Chemical and Physical Properties

Names and Identifiers

    • 1,2-dihydro-3-methyl-2-oxo-4-Pyridinecarboxylic acid
    • 4-Pyridinecarboxylicacid, 1,2-dihydro-3-methyl-2-oxo-
    • 3-methyl-2-pyridone-4-carboxylic acid
    • 4-Pyridinecarboxylicacid,1,2-dihydro-3-methyl-2-oxo-(9CI)
    • ACMC-20ms6b
    • AG-D-56104
    • CTK0H0206
    • SureCN1767848
    • SureCN5227532
    • 1,2-Dihydro-3-Methyl-2-oxo-pyridin-4-carboxylic acid
    • 3-METHYL-2-OXO-1H-PYRIDINE-4-CARBOXYLIC ACID
    • SCHEMBL1767848
    • DTXSID50631646
    • 2-Hydroxy-3-methylisonicotinic acid
    • 3-Methyl-2-oxo-1,2-dihydropyridine-4-carboxylic acid
    • 126798-27-4
    • 2-Hydroxy-3-methylisonicotinicacid
    • MDL: MFCD18803541
    • Inchi: 1S/C7H7NO3/c1-4-5(7(10)11)2-3-8-6(4)9/h2-3H,1H3,(H,8,9)(H,10,11)
    • InChI Key: BLZQLOJKKDNYHL-UHFFFAOYSA-N
    • SMILES: O=C1C(C)=C(C(=O)O)C=CN1

Computed Properties

  • Exact Mass: 153.042593085g/mol
  • Monoisotopic Mass: 153.042593085g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 1
  • Complexity: 275
  • 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: -0.2
  • Topological Polar Surface Area: 66.4?2

1,2-dihydro-3-methyl-2-oxo-4-Pyridinecarboxylic acid Pricemore >>

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1,2-dihydro-3-methyl-2-oxo-4-Pyridinecarboxylic acid Related Literature

Additional information on 1,2-dihydro-3-methyl-2-oxo-4-Pyridinecarboxylic acid

1,2-Dihydro-3-Methyl-2-Oxo-4-Pyridinecarboxylic Acid: A Comprehensive Overview

1,2-Dihydro-3-Methyl-2-Oxo-4-Pyridinecarboxylic Acid (CAS No. 126798-27-4) is a compound of significant interest in the fields of organic chemistry and pharmacology. This compound, often abbreviated as DMPA, belongs to the class of pyridine derivatives and exhibits unique structural and functional properties that make it a valuable molecule for various applications. The pyridine ring serves as the core structure, with substituents at positions 3 and 4 contributing to its chemical diversity and biological activity.

The chemical structure of 1,2-dihydro-3-methyl-2-oxo-4-pyridinecarboxylic acid is characterized by a partially saturated pyridine ring system. The presence of a methyl group at position 3 and a carboxylic acid group at position 4 introduces significant electronic and steric effects, which influence its reactivity and interactions with biological systems. Recent studies have highlighted the potential of this compound in drug discovery, particularly in the development of antimicrobial agents and anticancer drugs.

One of the most promising applications of DMPA lies in its ability to inhibit bacterial growth. Researchers have demonstrated that this compound exhibits potent activity against a wide range of pathogens, including Gram-positive and Gram-negative bacteria. The mechanism of action involves interference with bacterial cell wall synthesis and disruption of membrane integrity, making it a potential candidate for next-generation antibiotics.

In addition to its antimicrobial properties, 1,2-dihydro-3-methyl-2-oxo-4-pyridinecarboxylic acid has shown remarkable anticancer activity in preclinical studies. Experimental data indicate that this compound induces apoptosis in cancer cells by targeting key signaling pathways involved in cell proliferation and survival. The selective toxicity towards cancer cells, coupled with minimal effects on normal cells, underscores its potential as a targeted therapy for various malignancies.

The synthesis of DMPA involves a multi-step process that typically begins with the preparation of the pyridine ring system. Recent advancements in synthetic methodologies have enabled the efficient production of this compound with high purity and yield. Techniques such as microwave-assisted synthesis and continuous flow chemistry have been employed to optimize the reaction conditions, ensuring scalability for industrial applications.

From an environmental perspective, the degradation pathways of 1,2-dihydro-3-methyl-2-oxo-4-pyridinecarboxylic acid have been studied to assess its impact on ecosystems. Results suggest that the compound undergoes rapid biodegradation under aerobic conditions, minimizing its persistence in the environment. This property is particularly important for its use in agricultural and pharmaceutical industries where environmental safety is a critical concern.

In conclusion, 1,2-dihydro-3-methyl-2-oxo-4-pyridinecarboxylic acid (CAS No. 126798-27-4) is a versatile compound with diverse applications in medicine and biotechnology. Its unique chemical properties, combined with recent advancements in synthesis and application research, position it as a key molecule for future innovations in drug development and material science.

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