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Atomfair 2,2,2-Trifluoroethyl phosphate C2H4F3O4P

Description 2,2,2-Trifluoroethyl phosphate (CAS No. 358-63-4) is a high-purity organophosphorus compound with the molecular formula C2H4F3O4P, also known by its IUPAC name 2,2,2-trifluoroethyl dihydrogen phosphate . This specialized chemical is widely utilized in advanced research and industrial applications due to its unique trifluoroethyl and phosphate functional groups. It is available in rigorously controlled batches to ensure consistency for sensitive experiments. Suitable for use as a reagent, intermediate, or additive in organic synthesis, catalysis, and material science, this compound is packaged under inert conditions to maintain stability. Store in a cool, dry place away from moisture and incompatible materials.

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Description

Description

2,2,2-Trifluoroethyl phosphate (CAS No. 358-63-4) is a high-purity organophosphorus compound with the molecular formula C2H4F3O4P, also known by its IUPAC name 2,2,2-trifluoroethyl dihydrogen phosphate. This specialized chemical is widely utilized in advanced research and industrial applications due to its unique trifluoroethyl and phosphate functional groups. It is available in rigorously controlled batches to ensure consistency for sensitive experiments. Suitable for use as a reagent, intermediate, or additive in organic synthesis, catalysis, and material science, this compound is packaged under inert conditions to maintain stability. Store in a cool, dry place away from moisture and incompatible materials.

  • CAS No: 358-63-4
  • Molecular Formula: C2H4F3O4P
  • Molecular Weight: 180.02
  • Exact Mass: 179.97993009
  • Monoisotopic Mass: 179.97993009
  • IUPAC Name: 2,2,2-trifluoroethyl dihydrogen phosphate
  • SMILES: C(C(F)(F)F)OP(=O)(O)O
  • Synonyms: 2,2,2-Trifluoroethyl phosphate, 2805-15-4, DTXSID90182329, Ethanol, 2,2,2-trifluoro-, dihydrogen phosphate, DTXCID50104820

Application

2,2,2-Trifluoroethyl phosphate serves as a key intermediate in the synthesis of fluorinated organic compounds, particularly in pharmaceutical and agrochemical research. Its trifluoroethyl group enhances metabolic stability in drug design, while the phosphate moiety enables further functionalization. Researchers also employ it as a flame retardant additive or electrolyte component in specialty batteries. Its reactivity makes it valuable for modifying surfaces or polymers to introduce phosphonate groups.

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