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Atomfair Phenyl 1H-imidazole-1-sulfonate C9H8N2O3S

Description Phenyl 1H-imidazole-1-sulfonate (CAS No. 1198183-95-7) is a high-purity sulfonate ester compound with the molecular formula C9H8N2O3S . This specialized chemical is designed for research and industrial applications requiring precise sulfonation or imidazole-based intermediates. The compound features a phenyl group bonded to a sulfonate ester linkage with a 1H-imidazole moiety, offering unique reactivity for organic synthesis, pharmaceutical development, and materials science. With a molecular weight of 224.24 g/mol, it is supplied as a solid with ??95% purity (HPLC) and is characterized by NMR and LC-MS for quality assurance. Store under inert conditions at 2-8??C to maintain stability.

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Description

Description

Phenyl 1H-imidazole-1-sulfonate (CAS No. 1198183-95-7) is a high-purity sulfonate ester compound with the molecular formula C9H8N2O3S. This specialized chemical is designed for research and industrial applications requiring precise sulfonation or imidazole-based intermediates. The compound features a phenyl group bonded to a sulfonate ester linkage with a 1H-imidazole moiety, offering unique reactivity for organic synthesis, pharmaceutical development, and materials science. With a molecular weight of 224.24 g/mol, it is supplied as a solid with ??95% purity (HPLC) and is characterized by NMR and LC-MS for quality assurance. Store under inert conditions at 2-8??C to maintain stability.

  • CAS No: 1198183-95-7
  • Molecular Formula: C9H8N2O3S
  • Molecular Weight: 224.24
  • Exact Mass: 224.02556330
  • Monoisotopic Mass: 224.02556330
  • IUPAC Name: phenyl imidazole-1-sulfonate
  • SMILES: C1=CC=C(C=C1)OS(=O)(=O)N2C=CN=C2
  • Synonyms: SCHEMBL16037143, Phenyl 1H-imidazole-1-sulfonate, NTKIVUNQWDCFDZ-UHFFFAOYSA-N, 1H-imidazole-1-sulfonic acid, phenyl ester, DB-180845

Application

Phenyl 1H-imidazole-1-sulfonate serves as a versatile reagent in organic synthesis, particularly for introducing sulfonate groups to imidazole scaffolds in drug discovery. It is employed in cross-coupling reactions and as a precursor for sulfonamide derivatives in medicinal chemistry. Researchers also utilize it in polymer science to modify functional group reactivity.

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