Description

N,N-Dimethyl-1,1,2,2,2-pentafluoroethanesulfonamide (CAS No. 1270179-76-4) is a highly fluorinated sulfonamide compound with the molecular formula C₄H₆F₅NO₂S. This specialty chemical is characterized by its unique pentafluoroethyl group attached to a sulfonamide backbone, making it a valuable intermediate in organic synthesis and fluorochemical research. The compound exhibits exceptional thermal and chemical stability due to the presence of strong carbon-fluorine bonds, making it suitable for applications requiring inert and non-reactive materials.

With a purity of ??95% (GC), this product is supplied as a clear, colorless to pale yellow liquid under standard conditions. It is soluble in common organic solvents such as dichloromethane, THF, and acetonitrile but exhibits limited solubility in water. Researchers will appreciate its utility in the development of novel fluorinated materials, electrolytes, and pharmaceuticals where fluorine incorporation is desired for enhanced properties such as lipophilicity, metabolic stability, or electronic effects.

Proper storage recommendations include keeping the product in a tightly sealed container under inert atmosphere at 2-8??C to maintain stability. Safety data sheets are available upon request, and all handling should be performed in a well-ventilated fume hood with appropriate personal protective equipment due to the potential hazards associated with fluorinated compounds.

CAS No: 1270179-76-4
Molecular Formula: C4H6F5NO2S
Molecular Weight: 227.16
Exact Mass: 227.00394042
Monoisotopic Mass: 227.00394042
IUPAC Name: 1,1,2,2,2-pentafluoro-N,N-dimethylethanesulfonamide
SMILES: CN(C)S(=O)(=O)C(C(F)(F)F)(F)F
Synonyms: N,N-Dimethyl-1,1,2,2,2-pentafluoroethanesulfonamide, SCHEMBL2058155, PZAGLLDCDLRHGR-UHFFFAOYSA-N, 1,1,2,2,2-pentafluoro-N,N-dimethylethanesulfonamide, N,N-dimethyl-1,1,2,2,2-pentafluoro-ethanesulfonamide

Application

This fluorinated sulfonamide serves as a versatile building block in pharmaceutical research, particularly in the development of fluorine-containing drug candidates where its unique electronic properties can influence bioavailability and binding affinity. In materials science, it finds use as a precursor for advanced fluoropolymers with enhanced chemical resistance and low surface energy characteristics. The compound’s stability also makes it suitable for investigation as a potential electrolyte additive in lithium-ion battery systems to improve performance at extreme temperatures.

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