Atomfair N-ethyl-N-methylsulfamoyl fluoride C3H8FNO2S

Description N-Ethyl-N-methylsulfamoyl fluoride (CAS: 1458771-72-6) is a specialized organofluorine compound with the molecular formula C3H8FNO2S . This high-purity reagent is designed for advanced research applications, particularly in medicinal chemistry and chemical biology. The compound features a sulfamoyl fluoride moiety, making it a valuable intermediate for the synthesis of sulfonamide derivatives and protease inhibitors. With a molecular weight of 141.16 g/mol, it is supplied as a clear to pale-yellow liquid under standard conditions. Our product undergoes rigorous QC testing including1H NMR,13C NMR, and HPLC analysis to ensure ??95% purity. Suitable for use in controlled laboratory environments only. Store under inert atmosphere…

Description

N-Ethyl-N-methylsulfamoyl fluoride (CAS: 1458771-72-6) is a specialized organofluorine compound with the molecular formula C₃H₈FNO₂S. This high-purity reagent is designed for advanced research applications, particularly in medicinal chemistry and chemical biology. The compound features a sulfamoyl fluoride moiety, making it a valuable intermediate for the synthesis of sulfonamide derivatives and protease inhibitors. With a molecular weight of 141.16 g/mol, it is supplied as a clear to pale-yellow liquid under standard conditions. Our product undergoes rigorous QC testing including ¹H NMR, ¹³C NMR, and HPLC analysis to ensure ??95% purity. Suitable for use in controlled laboratory environments only. Store under inert atmosphere at 2-8??C.

CAS No: 1458771-72-6
Molecular Formula: C3H8FNO2S
Molecular Weight: 141.17
Exact Mass: 141.02597783
Monoisotopic Mass: 141.02597783
IUPAC Name: N-ethyl-N-methylsulfamoyl fluoride
SMILES: CCN(C)S(=O)(=O)F
Synonyms: N-Ethyl-N-methylsulfamoyl fluoride, 1458771-72-6, 102-079-8, SCHEMBL26522952, CS-0258225

Application

This sulfamoyl fluoride derivative serves as a key building block in pharmaceutical research, particularly for developing covalent enzyme inhibitors. It demonstrates reactivity with serine proteases and other nucleophilic enzyme targets. Researchers utilize this compound for probing active sites in biochemical systems. The ethyl-methyl substitution pattern offers unique steric properties for structure-activity relationship studies. Applications extend to PET tracer development due to the fluorine moiety.

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