Atomfair N,N-diethyl-1,1,1-trifluoromethanesulfonamide C5H10F3NO2S

Description N,N-diethyl-1,1,1-trifluoromethanesulfonamide (CAS No. 357-39-1) is a high-purity fluorinated sulfonamide compound with the molecular formula C5H10F3NO2S . This specialty chemical is designed for advanced research and industrial applications, offering exceptional stability and reactivity due to its trifluoromethanesulfonamide (triflylamide) functional group. Its unique structure, featuring diethylamine substitution, makes it a valuable intermediate in organic synthesis, catalysis, and materials science. The compound is rigorously tested for purity (typically ??95-98% by GC or HPLC) and is available in various quantities to suit laboratory-scale and bulk requirements. Proper handling under inert conditions is recommended due to its moisture-sensitive nature.

Description

N,N-diethyl-1,1,1-trifluoromethanesulfonamide (CAS No. 357-39-1) is a high-purity fluorinated sulfonamide compound with the molecular formula C₅H₁₀F₃NO₂S. This specialty chemical is designed for advanced research and industrial applications, offering exceptional stability and reactivity due to its trifluoromethanesulfonamide (triflylamide) functional group. Its unique structure, featuring diethylamine substitution, makes it a valuable intermediate in organic synthesis, catalysis, and materials science. The compound is rigorously tested for purity (typically ??95-98% by GC or HPLC) and is available in various quantities to suit laboratory-scale and bulk requirements. Proper handling under inert conditions is recommended due to its moisture-sensitive nature.

CAS No: 357-39-1
Molecular Formula: C5H10F3NO2S
Molecular Weight: 205.20
Exact Mass: 205.03843422
Monoisotopic Mass: 205.03843422
IUPAC Name: N,N-diethyl-1,1,1-trifluoromethanesulfonamide
SMILES: CCN(CC)S(=O)(=O)C(F)(F)F
Synonyms: N,N-diethyl-1,1,1-trifluoromethanesulfonamide, 357-39-1, N,N-diethyl-trifluoromethanesulfonamide, SCHEMBL10180979, DTXSID701044478

Application

N,N-diethyl-1,1,1-trifluoromethanesulfonamide is widely used as a precursor in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its strong electron-withdrawing properties make it valuable in catalytic systems and as a ligand modifier in transition metal complexes. Researchers also employ it in the development of ionic liquids and specialty polymers where fluorine incorporation enhances thermal and chemical resistance.

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