Cas no 172208-06-9 (2-methoxy-5-nitro-3-Pyridinecarbonitrile)

2-Methoxy-5-nitro-3-pyridinecarbonitrile is a versatile heterocyclic compound featuring a pyridine core substituted with methoxy, nitro, and cyano functional groups. Its distinct molecular structure makes it valuable as an intermediate in pharmaceutical and agrochemical synthesis, particularly in the development of active ingredients. The electron-withdrawing nitro and cyano groups enhance reactivity, facilitating further functionalization, while the methoxy group contributes to solubility and stability. This compound is characterized by high purity and consistent performance, ensuring reliable results in research and industrial applications. Its utility in cross-coupling reactions and as a building block for complex molecules underscores its importance in organic and medicinal chemistry.
2-methoxy-5-nitro-3-Pyridinecarbonitrile structure
172208-06-9 structure
Product Name:2-methoxy-5-nitro-3-Pyridinecarbonitrile
CAS No:172208-06-9
MF:C7H5N3O3
MW:179.132900953293
CID:1107594
Update Time:2025-06-07

2-methoxy-5-nitro-3-Pyridinecarbonitrile Chemical and Physical Properties

Names and Identifiers

    • 2-methoxy-5-nitro-3-Pyridinecarbonitrile
    • 3-Pyridinecarbonitrile, 2-methoxy-5-nitro-
    • Inchi： 1S/C7H5N3O3/c1-13-7-5(3-8)2-6(4-9-7)10(11)12/h2,4H,1H3
    • InChI Key： WSZZFKBRZWYXEF-UHFFFAOYSA-N
    • SMILES： C1(OC)=NC=C([N+]([O-])=O)C=C1C#N

Experimental Properties

  • Density: 1.40±0.1 g/cm3(Predicted)
  • Boiling Point: 321.4±42.0 °C(Predicted)
  • pka: -4.08±0.20(Predicted)

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2-methoxy-5-nitro-3-Pyridinecarbonitrile Related Literature

Additional information on 2-methoxy-5-nitro-3-Pyridinecarbonitrile

Comprehensive Overview of 2-Methoxy-5-nitro-3-Pyridinecarbonitrile (CAS No. 172208-06-9)

2-Methoxy-5-nitro-3-Pyridinecarbonitrile (CAS No. 172208-06-9) is a specialized organic compound widely utilized in pharmaceutical and agrochemical research. Its unique molecular structure, featuring a methoxy group, nitro substituent, and cyano functionality, makes it a valuable intermediate in synthetic chemistry. Researchers and industries are increasingly interested in this compound due to its potential applications in drug discovery and material science.

The compound’s pyridine core is a key structural motif in many bioactive molecules, contributing to its relevance in modern medicinal chemistry. Recent studies highlight its role in the synthesis of heterocyclic compounds, which are pivotal in developing new therapeutics for diseases like cancer and infectious illnesses. This aligns with current trends in precision medicine and targeted drug delivery, topics frequently searched in scientific databases and AI-driven platforms.

From a technical perspective, 2-Methoxy-5-nitro-3-Pyridinecarbonitrile exhibits notable stability under standard laboratory conditions, making it suitable for multi-step synthesis. Its nitro group offers opportunities for further functionalization, a feature highly sought after in high-throughput screening and combinatorial chemistry. These attributes address common queries from researchers exploring scalable synthetic routes or structure-activity relationships (SAR).

Environmental and regulatory considerations are also critical in today’s research landscape. While 172208-06-9 is not classified as hazardous under major chemical inventories, its handling requires adherence to Good Laboratory Practices (GLP). This resonates with growing interest in green chemistry and sustainable synthesis, as evidenced by frequent searches for eco-friendly reagents and waste reduction strategies.

In the agrochemical sector, derivatives of 3-Pyridinecarbonitrile are investigated for their potential as crop protection agents. The methoxy and nitro substituents may enhance bioavailability or selectivity, addressing global demands for pesticide alternatives—a hot topic amid discussions on food security and climate-resilient agriculture.

Analytical characterization of this compound typically involves HPLC, NMR spectroscopy, and mass spectrometry, techniques frequently queried in academic and industrial settings. Its chromatographic behavior and spectral fingerprints are well-documented, supporting its use in quality control protocols—a concern for manufacturers optimizing batch-to-batch consistency.

Emerging applications include its exploration in organic electronics, where nitroaromatic compounds contribute to charge transport materials. This connects to trending searches on flexible electronics and energy storage solutions, highlighting the compound’s interdisciplinary potential.

To summarize, 2-Methoxy-5-nitro-3-Pyridinecarbonitrile (CAS No. 172208-06-9) bridges multiple scientific domains, from pharmaceutical development to advanced materials. Its versatility and relevance to contemporary research challenges ensure continued interest, as reflected in evolving search patterns and academic citations.

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