Atomfair 1,1,1,3,3,3-Hexafluoropropan-2-yl acetate C5H4F6O2

Description 1,1,1,3,3,3-Hexafluoropropan-2-yl acetate (CAS No. 6919-79-5) is a high-purity fluorinated organic compound with the molecular formula C5H4F6O2. This specialty chemical is characterized by its hexafluoroisopropyl acetate structure, offering unique reactivity and solubility properties due to the presence of six fluorine atoms. It is commonly utilized in advanced synthetic chemistry, pharmaceutical research, and materials science applications where fluorinated building blocks are required. The compound is supplied as a clear, colorless liquid with stringent quality control to ensure consistency for research and industrial use. Its stability and compatibility with various reaction conditions make it a valuable reagent for scientists exploring novel fluorinated…

Description

1,1,1,3,3,3-Hexafluoropropan-2-yl acetate (CAS No. 6919-79-5) is a high-purity fluorinated organic compound with the molecular formula C₅H₄F₆O₂. This specialty chemical is characterized by its hexafluoroisopropyl acetate structure, offering unique reactivity and solubility properties due to the presence of six fluorine atoms. It is commonly utilized in advanced synthetic chemistry, pharmaceutical research, and materials science applications where fluorinated building blocks are required. The compound is supplied as a clear, colorless liquid with stringent quality control to ensure consistency for research and industrial use. Its stability and compatibility with various reaction conditions make it a valuable reagent for scientists exploring novel fluorinated compounds.

CAS No: 6919-79-5
Molecular Formula: C5H4F6O2
Molecular Weight: 210.07
Exact Mass: 210.01154834
Monoisotopic Mass: 210.01154834
IUPAC Name: 1,1,1,3,3,3-hexafluoropropan-2-yl acetate
SMILES: CC(=O)OC(C(F)(F)F)C(F)(F)F
Synonyms: 1,1,1,3,3,3-hexafluoropropan-2-yl acetate, 6919-79-5, SCHEMBL4382076, JYWDFMIPOIWWDZ-UHFFFAOYSA-N, LMZHCMDKZAJNJS-UHFFFAOYSA-N

Application

1,1,1,3,3,3-Hexafluoropropan-2-yl acetate is widely employed as a fluorinated intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its electron-withdrawing properties enhance the reactivity of adjacent functional groups, making it useful for nucleophilic substitution reactions. Researchers also utilize this compound in the development of specialty polymers and coatings due to its ability to impart hydrophobicity and chemical resistance. Additionally, it serves as a precursor for the synthesis of other hexafluoroisopropyl-containing derivatives.

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