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Atomfair 10-Acetylphenothiazine C14H11NOS

Description 10-Acetylphenothiazine (CAS No. 1628-29-1) is a high-purity organic compound with the molecular formula C14H11NOS . This derivative of phenothiazine features an acetyl group at the 10-position, enhancing its reactivity and utility in synthetic chemistry. With an IUPAC name of 1-phenothiazin-10-ylethanone , this compound is a valuable intermediate for pharmaceuticals, agrochemicals, and materials science research. It is supplied as a crystalline solid with verified purity, ensuring consistency for advanced applications. Ideal for researchers requiring precise functionalization of the phenothiazine scaffold, this product is rigorously tested via HPLC, NMR, and mass spectrometry to meet stringent quality standards.

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Description

Description

10-Acetylphenothiazine (CAS No. 1628-29-1) is a high-purity organic compound with the molecular formula C14H11NOS. This derivative of phenothiazine features an acetyl group at the 10-position, enhancing its reactivity and utility in synthetic chemistry. With an IUPAC name of 1-phenothiazin-10-ylethanone, this compound is a valuable intermediate for pharmaceuticals, agrochemicals, and materials science research. It is supplied as a crystalline solid with verified purity, ensuring consistency for advanced applications. Ideal for researchers requiring precise functionalization of the phenothiazine scaffold, this product is rigorously tested via HPLC, NMR, and mass spectrometry to meet stringent quality standards.

  • CAS No: 1628-29-1
  • Molecular Formula: C14H11NOS
  • Molecular Weight: 241.31
  • Exact Mass: 241.05613515
  • Monoisotopic Mass: 241.05613515
  • IUPAC Name: 1-phenothiazin-10-ylethanone
  • SMILES: CC(=O)N1C2=CC=CC=C2SC3=CC=CC=C31
  • Synonyms: 1628-29-1, 1-(10H-phenothiazin-10-yl)ethanone, 10-Acetylphenothiazine, Methyl phenothiazin-10-yl ketone, 10-Acetyl-10H-phenothiazine

Application

10-Acetylphenothiazine serves as a versatile building block in the synthesis of neuroactive compounds, including antipsychotic and antihistamine drug candidates. Its acetyl group enables further derivatization via condensation or reduction reactions, making it valuable for medicinal chemistry optimization. Researchers also employ it in photodynamic therapy studies due to phenothiazine’s electron-transfer properties. Additionally, it finds use in polymer science as a precursor for conductive materials.

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