Atomfair 1,1,1-trifluoro-N-methyl-methanesulfonamide C2H4F3NO2S

Description 1,1,1-Trifluoro-N-methylmethanesulfonamide (CAS No. 34310-29-7) is a high-purity fluorinated sulfonamide compound with the molecular formula C2H4F3NO2S. This specialty chemical is designed for advanced research and industrial applications, offering exceptional stability and reactivity due to its trifluoromethyl and sulfonamide functional groups. It is supplied as a clear, colorless liquid with a high degree of purity (>98%) to ensure consistency in synthetic and analytical workflows. Ideal for use in organic synthesis, pharmaceuticals, and materials science, this compound is rigorously tested for quality, including GC-MS and NMR verification. Proper storage under inert conditions is recommended to maintain its integrity.

Description

1,1,1-Trifluoro-N-methylmethanesulfonamide (CAS No. 34310-29-7) is a high-purity fluorinated sulfonamide compound with the molecular formula C₂H₄F₃NO₂S. This specialty chemical is designed for advanced research and industrial applications, offering exceptional stability and reactivity due to its trifluoromethyl and sulfonamide functional groups. It is supplied as a clear, colorless liquid with a high degree of purity (>98%) to ensure consistency in synthetic and analytical workflows. Ideal for use in organic synthesis, pharmaceuticals, and materials science, this compound is rigorously tested for quality, including GC-MS and NMR verification. Proper storage under inert conditions is recommended to maintain its integrity.

CAS No: 34310-29-7
Molecular Formula: C2H4F3NO2S
Molecular Weight: 163.12
Exact Mass: 162.99148403
Monoisotopic Mass: 162.99148403
IUPAC Name: 1,1,1-trifluoro-N-methylmethanesulfonamide
SMILES: CNS(=O)(=O)C(F)(F)F
Synonyms: 1,1,1-trifluoro-N-methyl-methanesulfonamide, 839-801-2, 34310-29-7, N-METHYLTRIFLUOROMETHANESULFONAMIDE, N-methyl trifluoromethanesulfonamide

Application

1,1,1-Trifluoro-N-methylmethanesulfonamide is widely utilized as a versatile building block in organic synthesis, particularly in the preparation of fluorinated sulfonamide derivatives. Its electron-withdrawing properties make it valuable in pharmaceutical research for designing bioactive molecules. Additionally, it serves as a key intermediate in the development of specialty polymers and electrolytes for advanced battery systems. Researchers also employ it in catalysis and ligand design due to its unique structural features.

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