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Atomfair N-(2,2,2-Trifluoroethyl)thiophene-2-sulfonamide C6H6F3NO2S2

Description N-(2,2,2-Trifluoroethyl)thiophene-2-sulfonamide (CAS No. 2326993-78-4) is a high-purity sulfonamide derivative designed for advanced research and industrial applications. With the molecular formula C6H6F3NO2S2, this compound features a thiophene-2-sulfonamide scaffold coupled with a 2,2,2-trifluoroethyl group, offering unique reactivity and potential in medicinal chemistry, agrochemical development, and material science. Its structural motif is valuable for designing enzyme inhibitors, ligands, and fluorinated building blocks. Each batch undergoes rigorous QC testing (HPLC, NMR) to ensure ??95% purity, packaged under inert conditions for stability. Available in scalable quantities with custom synthesis options.

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Description

Description

N-(2,2,2-Trifluoroethyl)thiophene-2-sulfonamide (CAS No. 2326993-78-4) is a high-purity sulfonamide derivative designed for advanced research and industrial applications. With the molecular formula C6H6F3NO2S2, this compound features a thiophene-2-sulfonamide scaffold coupled with a 2,2,2-trifluoroethyl group, offering unique reactivity and potential in medicinal chemistry, agrochemical development, and material science. Its structural motif is valuable for designing enzyme inhibitors, ligands, and fluorinated building blocks. Each batch undergoes rigorous QC testing (HPLC, NMR) to ensure ??95% purity, packaged under inert conditions for stability. Available in scalable quantities with custom synthesis options.

  • CAS No: 2326993-78-4
  • Molecular Formula: C6H6F3NO2S2
  • Molecular Weight: 245.2
  • Exact Mass: 244.97920527
  • Monoisotopic Mass: 244.97920527
  • IUPAC Name: N-(2,2,2-trifluoroethyl)thiophene-2-sulfonamide
  • SMILES: C1=CSC(=C1)S(=O)(=O)NCC(F)(F)F
  • Synonyms: N-(2,2,2-Trifluoroethyl)thiophene-2-sulfonamide, 2326993-78-4, AKOS039322324

Application

N-(2,2,2-Trifluoroethyl)thiophene-2-sulfonamide serves as a versatile intermediate in pharmaceutical research, particularly for developing protease inhibitors and kinase modulators due to its sulfonamide pharmacophore. The trifluoroethyl group enhances metabolic stability, making it valuable in PET tracer design. It also finds use in agrochemicals as a precursor for herbicidal sulfonamides. Researchers leverage its fluorinated thiophene core for electronic materials and ligand synthesis in catalysis.

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