Cas no 26482-00-8 (Pyridacylpyridinium Iodide)

Pyridacylpyridinium iodide is a quaternary ammonium compound characterized by its pyridinium-based structure, which imparts distinct chemical properties. This iodide salt is notable for its stability and solubility in polar solvents, making it suitable for applications in organic synthesis and catalysis. Its cationic nature facilitates interactions with anionic species, enhancing its utility in phase-transfer reactions. The compound’s rigid pyridinium core contributes to its thermal and chemical robustness, while the iodide counterion offers reactivity in halogen-exchange processes. Pyridacylpyridinium iodide is often employed in specialized chemical transformations, where its structural features enable precise control over reaction pathways. Its consistent performance and well-defined properties make it a reliable choice for research and industrial applications.
Pyridacylpyridinium Iodide structure
Pyridacylpyridinium Iodide structure
Product Name:Pyridacylpyridinium Iodide
CAS No:26482-00-8
MF:C12H11IN2O
MW:326.133014917374
MDL:MFCD01690884
CID:266568
PubChem ID:253661719
Update Time:2025-05-25

Pyridacylpyridinium Iodide Chemical and Physical Properties

Names and Identifiers

    • Pyridinium,1-[2-oxo-2-(2-pyridinyl)ethyl]-, iodide (1:1)
    • 1-[2-Oxo-2-(2-pyridyl)ethyl]pyridinium Iodide
    • 2-pyridin-1-ium-1-yl-1-pyridin-2-ylethanone,iodide
    • Pyridacylpyridinium Iodide
    • Pyridacylpyridinium Iodide
    • 1-(2-Pyridacyl)pyridinium iodide
    • 1-(2-Pyridylcarbonylmethyl)pyridinium iodide
    • 1-[2-(2-Pyridinyl)-2-oxoethyl]pyridinium iodide
    • Kr?hnke reagent
    • 1-((2-Pyridylcarbonyl)methyl)pyridinium iodide
    • 1-2-(Pyridiloacetyl)-pyridinium iodide [Polish]
    • Pyridinium, 1-((2-pyridylcarbonyl)methyl)-, iodide
    • 1-(2-Oxo-2-(pyridin-2-yl)ethyl)pyridin-1-ium iodide
    • 1-[2-Oxo-2-(2-Pyridyl)ethyl]pryridinium iodide
    • 1-[2-OXO-2-(PYRIDIN-2-YL)ETHYL]PYRIDIN-1-IUM IODIDE
    • 1-2-(Pyridiloacetyl)-pyridinium iodide
    • PYPI01
    • C12H11IN2O
    • Pyridini
    • 1-(2-oxo-2-(pyridin-2-yl)ethyl)pyridinium iodide
    • 2-pyridin-1-ium-1-yl-1-pyridin-2-ylethanone;iodide
    • 1-[2-(2-pyridyl)-2-oxoethyl]pyridinium iodide
    • CS-0450337
    • DTXSID10949350
    • 1-[2-oxo-2-(pyridyl)ethyl]pyridinium iodide
    • AS-70138
    • SCHEMBL1930231
    • Pan-W-15
    • D91872
    • 1-(2-Oxo-2-(pyridin-2-yl)ethyl)pyridin-1-iumiodide
    • AKOS027250778
    • 26482-00-8
    • 1-[2-Oxo-2-(2-pyridinyl)ethyl]pyridinium iodide, >=97.5% (HPLC)
    • MFCD01690884
    • O0438
    • Pyridinium, 1-[2-oxo-2-(2-pyridinyl)ethyl]-, iodide
    • BWAWQRQYQUSQEV-UHFFFAOYSA-M
    • MDL: MFCD01690884
    • Inchi: 1S/C12H11N2O.HI/c15-12(11-6-2-3-7-13-11)10-14-8-4-1-5-9-14;/h1-9H,10H2;1H/q+1;/p-1
    • InChI Key: BWAWQRQYQUSQEV-UHFFFAOYSA-M
    • SMILES: [I-].O=C(C1C=CC=CN=1)C[N+]1C=CC=CC=1

Computed Properties

  • Exact Mass: 314.9051
  • Monoisotopic Mass: 325.99161g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 3
  • Complexity: 212
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 33.8

Experimental Properties

  • PSA: 33.84

Pyridacylpyridinium Iodide Security Information

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Additional information on Pyridacylpyridinium Iodide

Comprehensive Overview of Pyridacylpyridinium Iodide (CAS No. 26482-00-8): Properties, Applications, and Innovations

Pyridacylpyridinium Iodide (CAS No. 26482-00-8) is a specialized organic compound that has garnered significant attention in recent years due to its unique chemical properties and versatile applications. This quaternary ammonium salt, characterized by its pyridinium core and iodide counterion, is widely studied in fields such as materials science, pharmaceuticals, and catalysis. Its molecular structure, which includes a pyridacyl moiety, contributes to its reactivity and functionality, making it a valuable tool for researchers and industries alike.

One of the most frequently searched questions about Pyridacylpyridinium Iodide is its role in advanced material synthesis. Recent studies highlight its use as a key intermediate in the development of ionic liquids, which are celebrated for their low volatility and high thermal stability. These properties align with the growing demand for green chemistry solutions, a hot topic in sustainability-driven research. Additionally, its application in photocatalysis has been explored, particularly in the context of renewable energy technologies, where it aids in the efficient conversion of light energy.

Another area of interest is the compound's potential in pharmaceutical research. While not a drug itself, Pyridacylpyridinium Iodide serves as a building block for synthesizing bioactive molecules. Researchers are investigating its derivatives for antimicrobial and antiviral properties, responding to the global need for novel therapeutics. This aligns with trending searches on drug discovery and antiviral agents, reflecting its relevance in contemporary science.

From a technical perspective, the compound's solubility in polar solvents like water and ethanol makes it highly adaptable for laboratory and industrial processes. Its stability under ambient conditions further enhances its practicality, a feature often queried in chemical handling forums. Analytical techniques such as NMR spectroscopy and mass spectrometry are commonly employed to characterize Pyridacylpyridinium Iodide, ensuring purity and consistency for critical applications.

Innovations in nanotechnology have also leveraged this compound. Its ionic nature facilitates the synthesis of nanostructured materials, which are pivotal in electronics and sensor development. This connection to emerging technologies resonates with searches related to smart materials and IoT devices, underscoring its interdisciplinary importance.

In summary, Pyridacylpyridinium Iodide (CAS No. 26482-00-8) stands at the intersection of multiple scientific frontiers. Its adaptability, coupled with rising interest in sustainable chemistry and biomedical innovation, ensures its continued relevance. As research progresses, this compound is poised to play an even greater role in addressing modern scientific and industrial challenges.

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