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Atomfair Triethyl(trifluoromethyl)silane C7H15F3Si

Description Triethyl(trifluoromethyl)silane (CAS No. 120120-26-5) is a highly versatile organosilicon compound with the molecular formula C7H15F3Si . This reagent is widely recognized for its utility in organic synthesis, particularly as a nucleophilic trifluoromethylating agent. Its unique structure, featuring a trifluoromethyl group bonded to a silicon center, enables efficient transfer of the -CF3moiety to electrophilic substrates under mild conditions. The compound is a clear, colorless to pale yellow liquid with excellent solubility in common organic solvents such as THF, DCM, and ether. With a purity of ??95% (GC), it is ideal for applications in pharmaceuticals, agrochemicals, and advanced material science. Proper…

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Description

Description

Triethyl(trifluoromethyl)silane (CAS No. 120120-26-5) is a highly versatile organosilicon compound with the molecular formula C7H15F3Si. This reagent is widely recognized for its utility in organic synthesis, particularly as a nucleophilic trifluoromethylating agent. Its unique structure, featuring a trifluoromethyl group bonded to a silicon center, enables efficient transfer of the -CF3 moiety to electrophilic substrates under mild conditions. The compound is a clear, colorless to pale yellow liquid with excellent solubility in common organic solvents such as THF, DCM, and ether. With a purity of ??95% (GC), it is ideal for applications in pharmaceuticals, agrochemicals, and advanced material science. Proper storage under inert atmosphere (e.g., argon or nitrogen) at 2-8??C ensures long-term stability.

  • CAS No: 120120-26-5
  • Molecular Formula: C7H15F3Si
  • Molecular Weight: 184.27
  • Exact Mass: 184.08951150
  • Monoisotopic Mass: 184.08951150
  • IUPAC Name: triethyl(trifluoromethyl)silane
  • SMILES: CC[Si](CC)(CC)C(F)(F)F
  • Synonyms: Triethyl(trifluoromethyl)silane, 120120-26-5, DTXSID60400825, DTXCID00351680, 628-487-0

Application

Triethyl(trifluoromethyl)silane is extensively used as a trifluoromethyl source in organic synthesis, enabling the introduction of -CF3 groups into aromatic and aliphatic systems. It is particularly valuable in nucleophilic trifluoromethylation reactions for pharmaceuticals and agrochemical intermediates. The compound also serves as a key reagent in the synthesis of fluorinated polymers and specialty materials. Its mild reaction conditions and high selectivity make it a preferred choice for researchers developing novel fluorinated compounds.

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