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Atomfair (Pentafluoroethyl)trimethylsilane C5H9F5Si

Description (Pentafluoroethyl)trimethylsilane (CAS No. 124898-13-1) is a highly specialized organofluorosilane compound with the molecular formula C5H9F5Si . This reagent features a pentafluoroethyl group bonded to a trimethylsilane moiety, offering unique reactivity for advanced synthetic applications. With a purity grade suitable for research and industrial use, it serves as a versatile building block in organofluorine chemistry, particularly in the synthesis of fluorinated materials, pharmaceuticals, and agrochemicals. Its thermal stability and volatility make it ideal for gas-phase deposition processes. Packaged under inert gas to ensure stability, this compound is available in various quantities to meet laboratory and bulk-scale demands.

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Description

Description

(Pentafluoroethyl)trimethylsilane (CAS No. 124898-13-1) is a highly specialized organofluorosilane compound with the molecular formula C5H9F5Si. This reagent features a pentafluoroethyl group bonded to a trimethylsilane moiety, offering unique reactivity for advanced synthetic applications. With a purity grade suitable for research and industrial use, it serves as a versatile building block in organofluorine chemistry, particularly in the synthesis of fluorinated materials, pharmaceuticals, and agrochemicals. Its thermal stability and volatility make it ideal for gas-phase deposition processes. Packaged under inert gas to ensure stability, this compound is available in various quantities to meet laboratory and bulk-scale demands.

  • CAS No: 124898-13-1
  • Molecular Formula: C5H9F5Si
  • Molecular Weight: 192.20
  • Exact Mass: 192.03936763
  • Monoisotopic Mass: 192.03936763
  • IUPAC Name: trimethyl(1,1,2,2,2-pentafluoroethyl)silane
  • SMILES: C[Si](C)(C)C(C(F)(F)F)(F)F
  • Synonyms: 124898-13-1, (Pentafluoroethyl)trimethylsilane, DTXSID60375367, DTXCID80326396, 673-912-5

Application

(Pentafluoroethyl)trimethylsilane is widely used as a fluorinating agent and silicon-based precursor in organic synthesis. It is employed in the preparation of fluorinated polymers and specialty materials with enhanced thermal and chemical resistance. Researchers utilize this compound in nucleophilic substitution reactions to introduce pentafluoroethyl groups into target molecules. Its applications extend to surface modification and coatings due to its ability to impart hydrophobic and oleophobic properties.

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