Atomfair 2,2-Difluoroethylacetate C4H6F2O2

Description 2,2-Difluoroethyl Acetate (CAS No. 1550-44-3) is a high-purity fluorinated ester compound with the molecular formula C4H6F2O2. This specialty chemical is widely utilized in advanced organic synthesis, pharmaceutical research, and material science due to its unique fluorinated structure. The compound is characterized by its clear liquid appearance, moderate volatility, and compatibility with a range of organic solvents. It is supplied in rigorously tested batches to ensure consistency in reactivity and purity, making it ideal for precision applications. Proper storage under inert conditions is recommended to maintain stability.

Description

2,2-Difluoroethyl Acetate (CAS No. 1550-44-3) is a high-purity fluorinated ester compound with the molecular formula C₄H₆F₂O₂. This specialty chemical is widely utilized in advanced organic synthesis, pharmaceutical research, and material science due to its unique fluorinated structure. The compound is characterized by its clear liquid appearance, moderate volatility, and compatibility with a range of organic solvents. It is supplied in rigorously tested batches to ensure consistency in reactivity and purity, making it ideal for precision applications. Proper storage under inert conditions is recommended to maintain stability.

CAS No: 1550-44-3
Molecular Formula: C4H6F2O2
Molecular Weight: 124.09
Exact Mass: 124.03358575
Monoisotopic Mass: 124.03358575
IUPAC Name: 2,2-difluoroethyl acetate
SMILES: CC(=O)OCC(F)F
Synonyms: 2,2-difluoroethyl acetate, 1550-44-3, 2,2-Difluoroethylacetate, DTXSID00165789, DTXCID2088280

Application

2,2-Difluoroethyl Acetate serves as a versatile building block in the synthesis of fluorinated pharmaceuticals and agrochemicals. It is employed as a precursor in the preparation of complex molecules where the difluoroethyl group enhances metabolic stability. Researchers also utilize this compound in polymer chemistry to modify surface properties and introduce fluorine-containing functionalities. Its reactivity under mild conditions makes it suitable for controlled esterification and transesterification reactions.

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