Cas no 2229532-80-1 (3-fluoro-2-(oxiran-2-yl)pyridine)

3-Fluoro-2-(oxiran-2-yl)pyridine is a versatile epoxide-containing heterocyclic compound, characterized by the presence of a fluorine-substituted pyridine ring fused with an oxirane moiety. This structure imparts high reactivity, making it a valuable intermediate in organic synthesis, particularly for the development of pharmaceuticals and agrochemicals. The fluorine atom enhances metabolic stability and binding affinity, while the oxirane group offers a reactive site for ring-opening reactions, enabling further functionalization. Its well-defined stereochemistry and purity ensure consistent performance in nucleophilic and electrophilic transformations. Suitable for use in medicinal chemistry and material science, this compound is optimized for applications requiring precise molecular modifications.
3-fluoro-2-(oxiran-2-yl)pyridine structure
2229532-80-1 structure
Product Name:3-fluoro-2-(oxiran-2-yl)pyridine
CAS No:2229532-80-1
MF:C7H6FNO
MW:139.127045154572
CID:6233682
PubChem ID:165880392
Update Time:2025-10-05

3-fluoro-2-(oxiran-2-yl)pyridine Chemical and Physical Properties

Names and Identifiers

    • 3-fluoro-2-(oxiran-2-yl)pyridine
    • 2229532-80-1
    • EN300-1790878
    • Inchi: 1S/C7H6FNO/c8-5-2-1-3-9-7(5)6-4-10-6/h1-3,6H,4H2
    • InChI Key: NMBNFDHODWCPJS-UHFFFAOYSA-N
    • SMILES: FC1=CC=CN=C1C1CO1

Computed Properties

  • Exact Mass: 139.043341977g/mol
  • Monoisotopic Mass: 139.043341977g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 1
  • Complexity: 131
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 0.4
  • Topological Polar Surface Area: 25.4?2

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Additional information on 3-fluoro-2-(oxiran-2-yl)pyridine

3-Fluoro-2-(oxiran-2-yl)pyridine (CAS No. 2229532-80-1): A Versatile Building Block in Modern Chemistry

The compound 3-fluoro-2-(oxiran-2-yl)pyridine (CAS No. 2229532-80-1) represents an important class of heterocyclic compounds that has gained significant attention in pharmaceutical and materials chemistry. This epoxide-containing pyridine derivative combines the unique electronic properties of both fluorine and epoxy functional groups, making it a valuable intermediate for various synthetic applications.

From a structural perspective, 3-fluoro-2-(oxiran-2-yl)pyridine features a pyridine ring substituted with fluorine at the 3-position and an oxirane (epoxide) moiety at the 2-position. This particular arrangement creates multiple reactive sites that can be exploited in synthetic transformations. The presence of both fluoropyridine and epoxide functionalities in a single molecule offers unique opportunities for creating complex molecular architectures.

Recent literature highlights the growing importance of fluorinated heterocycles in drug discovery, with 3-fluoro-2-(oxiran-2-yl)pyridine serving as a key precursor for bioactive molecules. The compound's ability to participate in ring-opening reactions with various nucleophiles makes it particularly valuable for constructing molecules with potential pharmaceutical applications. Researchers are actively exploring its use in developing new kinase inhibitors and central nervous system (CNS) active compounds.

The synthetic utility of 3-fluoro-2-(oxiran-2-yl)pyridine extends beyond medicinal chemistry. In materials science, this compound has shown promise as a building block for functional polymers and advanced materials. The epoxy group can undergo polymerization or cross-linking reactions, while the fluoropyridine moiety can influence the electronic properties of the resulting materials. This dual functionality makes it attractive for developing new materials with tailored properties.

From a commercial perspective, the demand for specialty fluorinated compounds like 3-fluoro-2-(oxiran-2-yl)pyridine has been steadily increasing. Pharmaceutical companies and research institutions are particularly interested in this compound as it can serve as a versatile intermediate in the synthesis of more complex molecules. The global market for fluorinated building blocks is expected to grow significantly in the coming years, driven by the expanding applications in life sciences and materials development.

When working with 3-fluoro-2-(oxiran-2-yl)pyridine, researchers should consider several important factors. The compound's stability, reactivity, and storage conditions are crucial for successful applications. Proper handling procedures should be followed to maintain the integrity of both the epoxide ring and the fluoropyridine system. Analytical techniques such as NMR spectroscopy and mass spectrometry are typically employed to characterize and verify the compound's purity.

Recent advances in synthetic methodology have improved the accessibility of 3-fluoro-2-(oxiran-2-yl)pyridine and related compounds. Modern catalytic approaches have enabled more efficient preparation of such multifunctional heterocycles, reducing production costs and environmental impact. These developments are particularly important as the chemical industry moves toward more sustainable practices.

The unique combination of fluorine and epoxy groups in 3-fluoro-2-(oxiran-2-yl)pyridine offers interesting possibilities for structure-activity relationship studies. Medicinal chemists can exploit the compound's reactivity to systematically modify its structure and evaluate biological effects. This approach has led to discoveries in various therapeutic areas, including potential treatments for neurological disorders and inflammatory conditions.

In the context of green chemistry, researchers are exploring new ways to utilize 3-fluoro-2-(oxiran-2-yl)pyridine in environmentally friendly processes. The compound's ability to participate in atom-economical transformations makes it attractive for sustainable synthesis. Recent publications have demonstrated its use in catalytic reactions that minimize waste generation and energy consumption.

Looking toward future applications, 3-fluoro-2-(oxiran-2-yl)pyridine is poised to play an important role in emerging technologies. Its potential uses in bioimaging probes, electronic materials, and catalysis are currently under investigation. The compound's versatility ensures that it will remain relevant across multiple scientific disciplines for years to come.

For researchers considering working with 3-fluoro-2-(oxiran-2-yl)pyridine, it's important to consult the latest literature and patent filings to understand its full potential. The compound's applications continue to expand as new synthetic methods and analytical techniques become available. Proper characterization and quality control are essential when using this intermediate in complex synthetic routes.

The development of 3-fluoro-2-(oxiran-2-yl)pyridine derivatives has opened new avenues in chemical biology. Scientists are exploring how subtle modifications to this scaffold can influence molecular recognition and binding properties. These studies contribute to our fundamental understanding of molecular interactions while potentially leading to practical applications in drug discovery and materials science.

As the chemical industry evolves, compounds like 3-fluoro-2-(oxiran-2-yl)pyridine will continue to bridge the gap between academic research and industrial applications. Their ability to serve as versatile building blocks makes them invaluable tools for innovation across multiple sectors. The ongoing research into this and related compounds promises to yield exciting developments in the near future.

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