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Atomfair Sulfamoyl fluoride, N,N-dimethyl- C2H6FNO2S

Description Sulfamoyl fluoride, N,N-dimethyl- (CAS No. 354-44-9) is a highly specialized organosulfur compound with the molecular formula C2H6FNO2S. This chemical is characterized by its sulfamoyl fluoride functional group, where the nitrogen atoms are substituted with methyl groups, resulting in the IUPAC name N,N-dimethylsulfamoyl fluoride . It is a valuable reagent in organic synthesis and medicinal chemistry, particularly in the development of sulfonamide-based compounds. The compound is supplied as a high-purity material, ensuring consistency and reliability for research applications. Proper handling under inert conditions is recommended due to its reactive fluoride moiety.

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Description

Description

Sulfamoyl fluoride, N,N-dimethyl- (CAS No. 354-44-9) is a highly specialized organosulfur compound with the molecular formula C2H6FNO2S. This chemical is characterized by its sulfamoyl fluoride functional group, where the nitrogen atoms are substituted with methyl groups, resulting in the IUPAC name N,N-dimethylsulfamoyl fluoride. It is a valuable reagent in organic synthesis and medicinal chemistry, particularly in the development of sulfonamide-based compounds. The compound is supplied as a high-purity material, ensuring consistency and reliability for research applications. Proper handling under inert conditions is recommended due to its reactive fluoride moiety.

  • CAS No: 354-44-9
  • Molecular Formula: C2H6FNO2S
  • Molecular Weight: 127.14
  • Exact Mass: 127.01032777
  • Monoisotopic Mass: 127.01032777
  • IUPAC Name: N,N-dimethylsulfamoyl fluoride
  • SMILES: CN(C)S(=O)(=O)F
  • Synonyms: Dimethylsulfamoyl fluoride, N,N-dimethylsulfamoyl fluoride, 354-44-9, Sulfamoyl fluoride, N,N-dimethyl-, Sulfamoyl fluoride, dimethyl-

Application

Sulfamoyl fluoride, N,N-dimethyl- is primarily used as a key intermediate in the synthesis of biologically active sulfonamide derivatives. It serves as a versatile building block in pharmaceutical research, particularly for protease inhibition studies. The compound’s reactivity with nucleophiles makes it useful in the development of covalent enzyme inhibitors. Researchers also employ it in the preparation of fluorinated sulfonamides for agrochemical applications.

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