Atomfair N-ethyl-N-methyl-trifluoromethanesulfonamide C4H8F3NO2S

Description N-ethyl-N-methyl-trifluoromethanesulfonamide (CAS No. 1427176-14-4) is a high-purity fluorinated sulfonamide compound with the molecular formula C4H8F3NO2S . This specialty chemical is characterized by its unique trifluoromethanesulfonamide structure, offering exceptional thermal stability and chemical resistance. It is synthesized under stringent quality control measures to ensure >98% purity, as verified by GC-MS and NMR analysis. The compound is supplied as a clear, colorless liquid with a molecular weight of 191.17 g/mol, boiling point of approximately 185-190??C, and density of 1.42 g/cm3. Ideal for advanced research applications, it is packaged under inert gas in amber glass bottles to prevent degradation. Key applications include…

Description

N-ethyl-N-methyl-trifluoromethanesulfonamide (CAS No. 1427176-14-4) is a high-purity fluorinated sulfonamide compound with the molecular formula C₄H₈F₃NO₂S. This specialty chemical is characterized by its unique trifluoromethanesulfonamide structure, offering exceptional thermal stability and chemical resistance. It is synthesized under stringent quality control measures to ensure >98% purity, as verified by GC-MS and NMR analysis. The compound is supplied as a clear, colorless liquid with a molecular weight of 191.17 g/mol, boiling point of approximately 185-190??C, and density of 1.42 g/cm³. Ideal for advanced research applications, it is packaged under inert gas in amber glass bottles to prevent degradation. Key applications include electrolyte additives for lithium-ion batteries, catalysts in organic synthesis, and as a precursor for pharmaceutical intermediates. Store in a cool, dry place at 2-8??C.

CAS No: 1427176-14-4
Molecular Formula: C4H8F3NO2S
Molecular Weight: 191.17
Exact Mass: 191.02278416
Monoisotopic Mass: 191.02278416
IUPAC Name: N-ethyl-1,1,1-trifluoro-N-methylmethanesulfonamide
SMILES: CCN(C)S(=O)(=O)C(F)(F)F
Synonyms: N-ethyl-N-methyl-trifluoromethanesulfonamide, 1427176-14-4, SCHEMBL10198481, XGOZXWSUGWDOOI-UHFFFAOYSA-N, N-ethyl-N-methyl-1,1,1-trifluoro-methanesulfonamide

Application

N-ethyl-N-methyl-trifluoromethanesulfonamide serves as a versatile building block in organic synthesis, particularly for introducing trifluoromethanesulfonamide groups into target molecules. Its electron-withdrawing properties make it valuable as an electrolyte additive in high-voltage lithium-ion batteries, where it enhances thermal stability and cycling performance. Researchers also utilize this compound in the development of novel pharmaceuticals and agrochemicals due to its ability to modulate bioavailability and metabolic stability.

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