Cas no 79802-73-6 (3,3-Difluorodihydrofuran-2,5-dione)

3,3-Difluorodihydrofuran-2,5-dione is a fluorinated heterocyclic compound featuring a dihydrofuran-2,5-dione core with two fluorine atoms at the 3-position. This structure imparts unique reactivity and stability, making it a valuable intermediate in organic synthesis, particularly for the preparation of fluorinated derivatives. The presence of fluorine enhances electrophilicity, facilitating nucleophilic addition reactions, while the cyclic anhydride moiety allows for further functionalization. Its applications include the development of pharmaceuticals, agrochemicals, and specialty materials where fluorination is desired for improved metabolic stability or physicochemical properties. The compound's well-defined reactivity profile and compatibility with diverse synthetic conditions underscore its utility in advanced chemical research and industrial processes.
3,3-Difluorodihydrofuran-2,5-dione structure
79802-73-6 structure
Product Name:3,3-Difluorodihydrofuran-2,5-dione
CAS No:79802-73-6
MF:C4H2F2O3
MW:136.053688526154
MDL:MFCD27928973
CID:531934
PubChem ID:13189243
Update Time:2025-05-22

3,3-Difluorodihydrofuran-2,5-dione Chemical and Physical Properties

Names and Identifiers

    • 2,5-Furandione, 3,3-difluorodihydro-
    • 3,3-difluorooxolane-2,5-dione
    • 3,3-difluorodihydrofuran-2,5-dione
    • DTXSID20525947
    • 2,2-difluorosuccinic anhydride
    • DL-0724
    • AT12560
    • CS-0130115
    • EN300-2009475
    • AKOS024124456
    • 79802-73-6
    • SCHEMBL4419149
    • 3,3-Difluorodihydrofuran-2,5-dione
    • MDL: MFCD27928973
    • Inchi: 1S/C4H2F2O3/c5-4(6)1-2(7)9-3(4)8/h1H2
    • InChI Key: WPSQLIQLGFFWTR-UHFFFAOYSA-N
    • SMILES: FC1(C(=O)OC(C1)=O)F

Computed Properties

  • Exact Mass: 135.99720025g/mol
  • Monoisotopic Mass: 135.99720025g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 0
  • Complexity: 175
  • 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: 0.3
  • Topological Polar Surface Area: 43.4?2

Experimental Properties

  • Density: 1.5±0.1 g/cm3
  • Melting Point: NA
  • Boiling Point: 137.6±30.0 °C at 760 mmHg
  • Flash Point: 36.8±19.4 °C
  • Vapor Pressure: 7.0±0.3 mmHg at 25°C

3,3-Difluorodihydrofuran-2,5-dione Security Information

3,3-Difluorodihydrofuran-2,5-dione Pricemore >>

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Additional information on 3,3-Difluorodihydrofuran-2,5-dione

Recent Advances in the Application of 3,3-Difluorodihydrofuran-2,5-dione (CAS: 79802-73-6) in Chemical Biology and Pharmaceutical Research

3,3-Difluorodihydrofuran-2,5-dione (CAS: 79802-73-6) is a fluorinated heterocyclic compound that has garnered significant attention in recent years due to its versatile applications in chemical biology and pharmaceutical research. This compound, characterized by its unique difluorinated structure, serves as a valuable building block in the synthesis of bioactive molecules and functional materials. Recent studies have explored its potential in drug discovery, medicinal chemistry, and materials science, highlighting its role as a key intermediate in the development of novel therapeutics and advanced materials.

One of the most notable applications of 3,3-Difluorodihydrofuran-2,5-dione is its use in the synthesis of fluorinated analogs of biologically active compounds. Fluorination is a common strategy in medicinal chemistry to enhance the metabolic stability, bioavailability, and binding affinity of drug candidates. Researchers have successfully incorporated this compound into the design of fluorinated inhibitors targeting enzymes such as kinases and proteases, which are implicated in various diseases, including cancer and neurodegenerative disorders. The difluorinated moiety of the compound contributes to the improved pharmacokinetic properties of these inhibitors, making them promising candidates for further development.

In addition to its role in drug discovery, 3,3-Difluorodihydrofuran-2,5-dione has been investigated for its utility in materials science. Its ability to participate in cycloaddition reactions and other transformations makes it a valuable precursor for the synthesis of fluorinated polymers and functional materials. These materials exhibit enhanced thermal stability, chemical resistance, and unique electronic properties, making them suitable for applications in electronics, coatings, and biomedical devices. Recent advancements in synthetic methodologies have further expanded the scope of its applications, enabling the precise control of material properties at the molecular level.

The mechanistic insights into the reactivity of 3,3-Difluorodihydrofuran-2,5-dione have also been a focus of recent research. Studies employing computational chemistry and spectroscopic techniques have elucidated the electronic and steric effects of the difluorinated group on its reactivity. These findings have provided a deeper understanding of its behavior in various chemical transformations, facilitating the rational design of new synthetic routes and functional materials. Furthermore, the compound's compatibility with green chemistry principles, such as the use of catalytic processes and renewable solvents, has been explored, aligning with the growing emphasis on sustainable chemical practices.

Despite the progress made, challenges remain in the large-scale synthesis and application of 3,3-Difluorodihydrofuran-2,5-dione. Issues such as regioselectivity in reactions and the need for optimized purification methods are areas of ongoing research. Collaborative efforts between academia and industry are expected to address these challenges, paving the way for broader utilization of this compound in pharmaceutical and material science applications. Future research directions may include the development of novel catalytic systems and the exploration of its potential in emerging fields such as bioorthogonal chemistry and targeted drug delivery.

In conclusion, 3,3-Difluorodihydrofuran-2,5-dione (CAS: 79802-73-6) represents a versatile and promising compound in the realm of chemical biology and pharmaceutical research. Its unique structural features and reactivity profile have enabled its use in diverse applications, from drug discovery to advanced materials. Continued research and innovation in this area hold the potential to unlock new opportunities and address unmet needs in the field. This research brief underscores the importance of this compound and highlights the latest advancements in its application, providing valuable insights for researchers and industry professionals alike.

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