Atomfair 1,1,1-Trifluoro-N,N-dimethylmethanesulfonamide C3H6F3NO2S

Description 1,1,1-Trifluoro-N,N-dimethylmethanesulfonamide (CAS No. 28048-17-1) is a high-purity fluorinated sulfonamide compound with the molecular formula C3H6F3NO2S . This specialty chemical is characterized by its trifluoromethyl and dimethylsulfonamide functional groups, making it a valuable reagent for advanced synthetic and catalytic applications. It is supplied as a clear, colorless to pale-yellow liquid with exceptional stability under inert conditions. Ideal for researchers in organofluorine chemistry, this compound serves as a versatile building block for pharmaceuticals, agrochemicals, and materials science. Strict quality control ensures ??95% purity (GC), with detailed technical data available upon request. Store under nitrogen at 2-8??C to maintain optimal integrity.

Description

1,1,1-Trifluoro-N,N-dimethylmethanesulfonamide (CAS No. 28048-17-1) is a high-purity fluorinated sulfonamide compound with the molecular formula C₃H₆F₃NO₂S. This specialty chemical is characterized by its trifluoromethyl and dimethylsulfonamide functional groups, making it a valuable reagent for advanced synthetic and catalytic applications. It is supplied as a clear, colorless to pale-yellow liquid with exceptional stability under inert conditions. Ideal for researchers in organofluorine chemistry, this compound serves as a versatile building block for pharmaceuticals, agrochemicals, and materials science. Strict quality control ensures ??95% purity (GC), with detailed technical data available upon request. Store under nitrogen at 2-8??C to maintain optimal integrity.

CAS No: 28048-17-1
Molecular Formula: C3H6F3NO2S
Molecular Weight: 177.15
Exact Mass: 177.00713409
Monoisotopic Mass: 177.00713409
IUPAC Name: 1,1,1-trifluoro-N,N-dimethylmethanesulfonamide
SMILES: CN(C)S(=O)(=O)C(F)(F)F
Synonyms: 1,1,1-trifluoro-N,N-dimethylmethanesulfonamide, 881-285-6, 28048-17-1, N,N-DIMETHYLTRIFLUOROMETHANESULFONAMIDE, MFCD20366501

Application

1,1,1-Trifluoro-N,N-dimethylmethanesulfonamide is widely employed as a fluorinating agent and polar aprotic solvent in nucleophilic substitution reactions. Its strong electron-withdrawing properties make it effective in catalyzing Friedel-Crafts acylations and facilitating trifluoromethylation processes. Researchers utilize this compound in the synthesis of bioactive molecules, particularly in medicinal chemistry for introducing trifluoromethyl groups into heterocyclic scaffolds. It also finds niche applications in electrolyte formulations for lithium-ion batteries due to its thermal stability.

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