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Atomfair 2-Acetamido-5-aminobenzenesulfonic acid C8H10N2O4S

Description 2-Acetamido-5-aminobenzenesulfonic acid (CAS No. 6973-05-3) is a high-purity sulfonic acid derivative with the molecular formula C8H10N2O4S . This compound features both acetamido and amino functional groups on a benzene ring, making it a versatile intermediate for organic synthesis and pharmaceutical research. Its sulfonic acid group enhances solubility in aqueous and polar solvents, ideal for reaction optimization and analytical applications. Suitable for researchers and industrial scientists, this product is rigorously tested for purity and consistency, ensuring reliable performance in synthetic workflows. Available in various quantities to accommodate lab-scale experiments and bulk production needs.

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Description

Description

2-Acetamido-5-aminobenzenesulfonic acid (CAS No. 6973-05-3) is a high-purity sulfonic acid derivative with the molecular formula C8H10N2O4S. This compound features both acetamido and amino functional groups on a benzene ring, making it a versatile intermediate for organic synthesis and pharmaceutical research. Its sulfonic acid group enhances solubility in aqueous and polar solvents, ideal for reaction optimization and analytical applications. Suitable for researchers and industrial scientists, this product is rigorously tested for purity and consistency, ensuring reliable performance in synthetic workflows. Available in various quantities to accommodate lab-scale experiments and bulk production needs.

  • CAS No: 6973-05-3
  • Molecular Formula: C8H10N2O4S
  • Molecular Weight: 230.24
  • Exact Mass: 230.03612798
  • Monoisotopic Mass: 230.03612798
  • IUPAC Name: 2-acetamido-5-aminobenzenesulfonic acid
  • SMILES: CC(=O)NC1=C(C=C(C=C1)N)S(=O)(=O)O
  • Synonyms: 2-acetamido-5-aminobenzenesulfonic acid, 6973-05-3, 2-Acetamido-5-aminobenzenesulphonic acid, Q7KG8JB4AD, NSC-36987

Application

2-Acetamido-5-aminobenzenesulfonic acid is widely used as a key intermediate in the synthesis of dyes, pigments, and pharmaceutical compounds. Its reactive amino and sulfonic acid groups facilitate coupling reactions and derivatization for specialty chemical production. Researchers also employ it in the development of sulfonamide-based drugs and as a precursor for advanced material science applications.

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