Cas no 412032-33-8 (N,N-Dimethyl-6-oxo-1,6-dihydropyridine-3-carboxamide)

N,N-Dimethyl-6-oxo-1,6-dihydropyridine-3-carboxamide is a heterocyclic compound featuring a pyridine core with a carboxamide substituent at the 3-position and a carbonyl group at the 6-position. This structure imparts unique reactivity, making it a valuable intermediate in pharmaceutical and agrochemical synthesis. Its electron-rich pyridone moiety enables participation in diverse chemical transformations, including nucleophilic substitutions and metal-catalyzed couplings. The dimethylamide group enhances solubility in organic solvents, facilitating downstream functionalization. The compound’s stability under standard conditions ensures reliable handling and storage. Its versatility as a building block for bioactive molecules underscores its utility in medicinal chemistry research, particularly in the development of kinase inhibitors and other therapeutic agents.
N,N-Dimethyl-6-oxo-1,6-dihydropyridine-3-carboxamide structure
412032-33-8 structure
Product Name:N,N-Dimethyl-6-oxo-1,6-dihydropyridine-3-carboxamide
CAS No:412032-33-8
MF:C8H10N2O2
MW:166.177201747894
MDL:MFCD11174155
CID:1020662
PubChem ID:19692588
Update Time:2025-10-23

N,N-Dimethyl-6-oxo-1,6-dihydropyridine-3-carboxamide Chemical and Physical Properties

Names and Identifiers

    • 3-Pyridinecarboxamide,1,6-dihydro-N,N-dimethyl-6-oxo-(9CI)
    • N,N-Dimethyl-6-oxo-1,6-dihydropyridine-3-carboxamide
    • MDL: MFCD11174155
    • Inchi: 1S/C8H10N2O2/c1-10(2)8(12)6-3-4-7(11)9-5-6/h3-5H,1-2H3,(H,9,11)
    • InChI Key: OWMPZDOGVWJQLN-UHFFFAOYSA-N
    • SMILES: O=C(C1C=CC(NC=1)=O)N(C)C

Computed Properties

  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 1
  • Complexity: 277
  • XLogP3: -0.6
  • Topological Polar Surface Area: 49.4

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Additional information on N,N-Dimethyl-6-oxo-1,6-dihydropyridine-3-carboxamide

Comprehensive Overview of N,N-Dimethyl-6-oxo-1,6-dihydropyridine-3-carboxamide (CAS No. 412032-33-8)

N,N-Dimethyl-6-oxo-1,6-dihydropyridine-3-carboxamide, with the CAS number 412032-33-8, is a specialized organic compound that has garnered significant attention in pharmaceutical and biochemical research. This compound belongs to the pyridine derivative family, characterized by its unique 6-oxo-1,6-dihydropyridine core structure. Researchers and industries are increasingly interested in its potential applications due to its versatile chemical properties and relevance in drug discovery.

The molecular structure of N,N-Dimethyl-6-oxo-1,6-dihydropyridine-3-carboxamide features a carboxamide group attached to the pyridine ring, which enhances its reactivity and interaction with biological targets. This structural motif is commonly explored in the development of small-molecule inhibitors and enzyme modulators, making it a valuable scaffold in medicinal chemistry. Recent studies highlight its potential in addressing oxidative stress-related disorders and metabolic diseases, aligning with current health trends.

In the context of sustainable chemistry, CAS 412032-33-8 has been investigated for its eco-friendly synthesis routes. With growing demand for green chemistry solutions, researchers are optimizing its production to minimize waste and energy consumption. This aligns with global initiatives like the UN Sustainable Development Goals (SDGs), particularly in promoting responsible consumption and production.

From a commercial perspective, N,N-Dimethyl-6-oxo-1,6-dihydropyridine-3-carboxamide is often sought after by pharmaceutical intermediates suppliers and research laboratories. Its high purity grade and custom synthesis options make it a preferred choice for drug development projects. Additionally, its compatibility with high-throughput screening (HTS) platforms has expanded its utility in precision medicine applications.

The compound’s stability under various pH conditions and solvent systems further broadens its applicability. For instance, it has been tested in aqueous and organic media, demonstrating consistent performance in catalytic reactions and bioconjugation studies. Such properties are critical for biocompatibility assessments in nanotechnology and drug delivery systems.

Emerging trends in AI-driven drug discovery have also spotlighted CAS 412032-33-8. Computational models predict its interactions with protein targets, accelerating the identification of novel therapeutic agents. This synergy between cheminformatics and experimental validation underscores its role in modern pharmacology.

In summary, N,N-Dimethyl-6-oxo-1,6-dihydropyridine-3-carboxamide (412032-33-8) represents a multifaceted compound with promising scientific and industrial potential. Its structural elegance, combined with its alignment with health innovation and sustainability, positions it as a key player in advancing life sciences and material engineering.

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