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2043-55-2 | 1,1,1,2,2,3,3,4,4-Nonafluoro-6-iodohexane

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1,1,1,2,2,3,3,4,4-Nonafluoro-6-iodohexane (NFH) is an organofluorine compound with a wide range of applications in scientific research. It is a non-flammable and volatile compound with a boiling point of -36.5°C. NFH has been used as a reagent in a variety of organic reactions, including the synthesis of fluorinated co...

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CAS:2043-55-2 | 1,1,1,2,2,3,3,4,4-Nonafluoro-6-iodohexane ,Description

1,1,1,2,2,3,3,4,4-Nonafluoro-6-iodohexane (NFH) is an organofluorine compound with a wide range of applications in scientific research. It is a non-flammable and volatile compound with a boiling point of -36.5°C. NFH has been used as a reagent in a variety of organic reactions, including the synthesis of fluorinated compounds, and as a solvent for a variety of reactions. It is also used as a catalyst in the synthesis of organofluorine compounds. NFH is a versatile compound with many potential applications in scientific research.
 

Scientific Research Applications

 

  • Molecule-Based Electronics

    • The bifunctional 1-S(acetyl)-tris(pyrazolyl)alkanes synthesized from 1-chloro-6-iodohexane show promise in molecule-based electronics. Their molecular structures limit intermolecular interactions and exhibit slow relaxation of magnetization, which is essential for data storage and manipulation applications (Li et al., 2006).
  • Material Synthesis and Characterization

    • The substance is used in the synthesis of iodine-functionalized phenylalanine-based poly(ester urea)s (PEUs). The modulation of copolymer composition with this compound allows for adjusting the mechanical, thermal, and radiopacity properties of PEUs, making them valuable for medical devices requiring X-ray contrast (Li et al., 2015).
  • Synthesis of Deuterofluorocarbons

    • The compound is involved in the selective synthesis of deuterofluorocarbons, specifically 1-deuterononafluorobutane from 1-iodononafluorobutane. This process is important for creating substances with altered chemical and physical properties for industrial and pharmaceutical applications (Richardson et al., 2015).
  • Nuclear Medicine

    • Derivatives of this compound, like D-glucosamine iodine-labeled glucose derivatives, have been explored for their application in radionuclide diagnostics and therapy, particularly for conditions like rheumatoid arthritis (Ларькина et al., 2018) .
  • Microwave Synthesis of Ionic Liquids

    • The compound is used in microwave synthesis to create novel fluorinated ionic liquid surfactants. This synthesis pathway is valued for its speed and efficiency in producing surfactants with intriguing phase behavior and low surface tension, useful in various industrial and scientific applications (Breen et al., 2016).

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