Atomfair 4-Hydrazinylbenzenesulfonamide hydrochloride C6H10ClN3O2S

Description 4-Hydrazinylbenzenesulfonamide hydrochloride (CAS No. 17852-52-7) is a high-purity sulfonamide derivative with the molecular formula C6H10ClN3O2S. This compound is widely utilized in organic synthesis, pharmaceutical research, and biochemical applications due to its reactive hydrazinyl functional group. The hydrochloride salt form enhances stability and solubility, making it ideal for experimental workflows. With a molecular weight of 223.68 g/mol, it is supplied as a white to off-white crystalline powder, ensuring consistent performance in sensitive reactions. Suitable for researchers requiring precise sulfonamide modifications or hydrazine-based intermediates.

Description

Description

4-Hydrazinylbenzenesulfonamide hydrochloride (CAS No. 17852-52-7) is a high-purity sulfonamide derivative with the molecular formula C6H10ClN3O2S. This compound is widely utilized in organic synthesis, pharmaceutical research, and biochemical applications due to its reactive hydrazinyl functional group. The hydrochloride salt form enhances stability and solubility, making it ideal for experimental workflows. With a molecular weight of 223.68 g/mol, it is supplied as a white to off-white crystalline powder, ensuring consistent performance in sensitive reactions. Suitable for researchers requiring precise sulfonamide modifications or hydrazine-based intermediates.

  • CAS No: 17852-52-7
  • Molecular Formula: C6H10ClN3O2S
  • Molecular Weight: 223.68
  • Exact Mass: 223.0182254
  • Monoisotopic Mass: 223.0182254
  • IUPAC Name: 4-hydrazinylbenzenesulfonamide;hydrochloride
  • SMILES: C1=CC(=CC=C1NN)S(=O)(=O)N.Cl
  • Synonyms: 4-hydrazinylbenzenesulfonamide Hydrochloride, 479-480-2, 17852-52-7, 27918-19-0, 4-hydrazinobenzene-1-sulfonamide hydrochloride

Application

4-Hydrazinylbenzenesulfonamide hydrochloride serves as a key intermediate in the synthesis of sulfonamide-based pharmaceuticals, including antimicrobial and diuretic agents. Its hydrazinyl group enables conjugation with carbonyl compounds, facilitating the development of hydrazone derivatives for drug discovery. Researchers also employ it in the preparation of dyes and analytical reagents. The compound’s reactivity makes it valuable in heterocyclic chemistry and as a building block for specialized polymers.

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