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Atomfair 2,2,2-Trifluoroethyl Acetate C4H5F3O2

Description 2,2,2-Trifluoroethyl Acetate (CAS No. 406-95-1) is a high-purity fluorinated ester with the molecular formula C4H5F3O2. This specialized chemical is widely utilized in organic synthesis, pharmaceutical intermediates, and advanced material research due to its unique trifluoroethyl group. The compound is characterized by its clear, colorless appearance and distinctive ester-like odor. It is supplied in rigorously controlled conditions to ensure optimal stability and performance. Suitable for use in HPLC, GC-MS, and NMR applications , this reagent is ideal for researchers requiring precise fluorinated building blocks. Available in various packaging options to accommodate laboratory-scale and bulk industrial needs.

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Description

Description

2,2,2-Trifluoroethyl Acetate (CAS No. 406-95-1) is a high-purity fluorinated ester with the molecular formula C4H5F3O2. This specialized chemical is widely utilized in organic synthesis, pharmaceutical intermediates, and advanced material research due to its unique trifluoroethyl group. The compound is characterized by its clear, colorless appearance and distinctive ester-like odor. It is supplied in rigorously controlled conditions to ensure optimal stability and performance. Suitable for use in HPLC, GC-MS, and NMR applications, this reagent is ideal for researchers requiring precise fluorinated building blocks. Available in various packaging options to accommodate laboratory-scale and bulk industrial needs.

  • CAS No: 406-95-1
  • Molecular Formula: C4H5F3O2
  • Molecular Weight: 142.08
  • Exact Mass: 142.02416388
  • Monoisotopic Mass: 142.02416388
  • IUPAC Name: 2,2,2-trifluoroethyl acetate
  • SMILES: CC(=O)OCC(F)(F)F
  • Synonyms: 2,2,2-trifluoroethyl acetate, trifluoroethyl acetate, Ethanol, 2,2,2-trifluoro-, acetate, Acetic acid, 2,2,2-trifluoroethyl ester, UNII-EN07RVL78U

Application

2,2,2-Trifluoroethyl Acetate serves as a versatile reagent in fluorinated compound synthesis, particularly in pharmaceutical and agrochemical development. It is employed as a solvent or intermediate in nucleophilic substitution reactions due to its electron-withdrawing trifluoroethyl group. Researchers also utilize it in polymer chemistry to modify material properties such as hydrophobicity and thermal stability. Its compatibility with analytical techniques makes it valuable for method development in chromatography and spectrometry.

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