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Atomfair 4′-Mercaptoacetanilide C8H9NOS

Description 4′-Mercaptoacetanilide (CAS No. 1126-81-4) is a high-purity organic compound with the molecular formula C8H9NOS, widely utilized in research and industrial applications. This compound, also known as N-(4-sulfanylphenyl)acetamide, features a thiol (-SH) functional group, making it a versatile intermediate in organic synthesis, surface modification, and material science. Its well-defined structure and reactivity enable precise functionalization in the development of pharmaceuticals, polymers, and nanomaterials. Suitable for laboratory use, our 4′-Mercaptoacetanilide is rigorously tested for purity and stability, ensuring reliable performance in sensitive applications. Available in various quantities, it is ideal for researchers requiring consistent quality and traceability.

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Description

Description

4′-Mercaptoacetanilide (CAS No. 1126-81-4) is a high-purity organic compound with the molecular formula C8H9NOS, widely utilized in research and industrial applications. This compound, also known as N-(4-sulfanylphenyl)acetamide, features a thiol (-SH) functional group, making it a versatile intermediate in organic synthesis, surface modification, and material science. Its well-defined structure and reactivity enable precise functionalization in the development of pharmaceuticals, polymers, and nanomaterials. Suitable for laboratory use, our 4′-Mercaptoacetanilide is rigorously tested for purity and stability, ensuring reliable performance in sensitive applications. Available in various quantities, it is ideal for researchers requiring consistent quality and traceability.

  • CAS No: 1126-81-4
  • Molecular Formula: C8H9NOS
  • Molecular Weight: 167.23
  • Exact Mass: 167.04048508
  • Monoisotopic Mass: 167.04048508
  • IUPAC Name: N-(4-sulfanylphenyl)acetamide
  • SMILES: CC(=O)NC1=CC=C(C=C1)S
  • Synonyms: 4-Acetamidothiophenol, 1126-81-4, 4′-Mercaptoacetanilide, 4-Mercaptoacetanilide, EINECS 214-427-7

Application

4′-Mercaptoacetanilide is commonly employed as a key intermediate in organic synthesis, particularly in the preparation of thiol-functionalized compounds for surface chemistry and material science. Its reactive thiol group allows for covalent attachment to gold and other metal surfaces, making it valuable in biosensor and nanotechnology applications. Additionally, it serves as a precursor in pharmaceutical research for the development of novel drug candidates and bioactive molecules.

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