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Atomfair Trimethylsilyl 2,2-difluoro-2-(fluorosulfonyl)acetate C5H9F3O4SSi

Description Trimethylsilyl 2,2-difluoro-2-(fluorosulfonyl)acetate (CAS No. 120801-75-4) is a highly specialized organosilicon compound with the molecular formula C5H9F3O4SSi . This reagent is widely utilized in advanced synthetic organic chemistry and materials science due to its unique reactivity as a difluoroacetate derivative with a fluorosulfonyl group. The trimethylsilyl (TMS) moiety enhances its stability and solubility in non-polar solvents, making it ideal for controlled reactions. Suitable for researchers and industrial chemists, this compound is rigorously tested for purity and consistency, ensuring reliable performance in demanding applications. Store under inert conditions to maintain integrity.

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Description

Description

Trimethylsilyl 2,2-difluoro-2-(fluorosulfonyl)acetate (CAS No. 120801-75-4) is a highly specialized organosilicon compound with the molecular formula C5H9F3O4SSi. This reagent is widely utilized in advanced synthetic organic chemistry and materials science due to its unique reactivity as a difluoroacetate derivative with a fluorosulfonyl group. The trimethylsilyl (TMS) moiety enhances its stability and solubility in non-polar solvents, making it ideal for controlled reactions. Suitable for researchers and industrial chemists, this compound is rigorously tested for purity and consistency, ensuring reliable performance in demanding applications. Store under inert conditions to maintain integrity.

  • CAS No: 120801-75-4
  • Molecular Formula: C5H9F3O4SSi
  • Molecular Weight: 250.27
  • Exact Mass: 249.99429096
  • Monoisotopic Mass: 249.99429096
  • IUPAC Name: trimethylsilyl 2,2-difluoro-2-fluorosulfonylacetate
  • SMILES: C[Si](C)(C)OC(=O)C(F)(F)S(=O)(=O)F
  • Synonyms: 120801-75-4, Trimethylsilyl 2,2-difluoro-2-(fluorosulfonyl)acetate, DTXSID40380752, DTXCID70331777, trimethylsilyl 2-(fluorosulfonyl)difluoroacetate

Application

Trimethylsilyl 2,2-difluoro-2-(fluorosulfonyl)acetate is primarily employed as a key intermediate in the synthesis of fluorinated organic compounds, including pharmaceuticals and agrochemicals. Its reactive fluorosulfonyl group facilitates efficient introduction of fluorine atoms into target molecules, enabling precise structural modifications. Researchers also leverage its properties in polymer chemistry to create fluorinated materials with enhanced thermal and chemical resistance. Additionally, it serves as a versatile building block in organometallic catalysis and specialty reagent formulations.

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