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Atomfair 1,1,1-Trifluoro-2-iodoethane C2H2F3I

Description 1,1,1-Trifluoro-2-iodoethane (CAS No. 353-83-3) is a highly specialized fluorinated organic compound with the molecular formula C2H2F3I . This clear, volatile liquid is characterized by its trifluoromethyl group and reactive iodoethane moiety, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. With a purity grade of ??98%, our product is rigorously tested via GC-MS and NMR to ensure consistency for demanding applications. Ideal for nucleophilic substitution reactions, cross-coupling processes, and as a building block for fluorinated compounds, it is supplied in amber glass bottles under inert gas to prevent degradation. Store at 2-8??C in a well-ventilated area,…

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Description

Description

1,1,1-Trifluoro-2-iodoethane (CAS No. 353-83-3) is a highly specialized fluorinated organic compound with the molecular formula C2H2F3I. This clear, volatile liquid is characterized by its trifluoromethyl group and reactive iodoethane moiety, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. With a purity grade of ??98%, our product is rigorously tested via GC-MS and NMR to ensure consistency for demanding applications. Ideal for nucleophilic substitution reactions, cross-coupling processes, and as a building block for fluorinated compounds, it is supplied in amber glass bottles under inert gas to prevent degradation. Store at 2-8??C in a well-ventilated area, away from light and moisture. Hazard statements apply (H315, H319, H335).

  • CAS No: 353-83-3
  • Molecular Formula: C2H2F3I
  • Molecular Weight: 209.94
  • Exact Mass: 209.91533
  • Monoisotopic Mass: 209.91533
  • IUPAC Name: 1,1,1-trifluoro-2-iodoethane
  • SMILES: C(C(F)(F)F)I
  • Synonyms: 1,1,1-Trifluoro-2-iodoethane, 2-Iodo-1,1,1-trifluoroethane, 2,2,2-Trifluoroethyl iodide, Trifluoroethyl iodide, 1,1,1-Trifluoroiodoethane

Application

1,1,1-Trifluoro-2-iodoethane serves as a key reagent in the synthesis of fluorinated pharmaceuticals and agrochemicals, enabling the introduction of trifluoroethyl groups via cross-coupling reactions. It is widely used in palladium-catalyzed transformations, such as Heck and Suzuki couplings, to construct complex fluorinated architectures. Researchers also employ it as a precursor for radiolabeling compounds in PET imaging studies due to the lability of the iodine moiety.

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