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Atomfair 10-Acetylphenothiazine C14H11NOS CAS 1628-29-1

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

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.

Properties

  • CAS Number: 1628-29-1
  • Complexity: 285
  • IUPAC Name: 1-phenothiazin-10-ylethanone
  • InChI: InChI=1S/C14H11NOS/c1-10(16)15-11-6-2-4-8-13(11)17-14-9-5-3-7-12(14)15/h2-9H,1H3
  • InChI Key: DNVNQWUERFZASD-UHFFFAOYSA-N
  • Exact Mass: 241.05613515
  • Molecular Formula: C14H11NOS
  • Molecular Weight: 241.31
  • SMILES: CC(=O)N1C2=CC=CC=C2SC3=CC=CC=C31
  • Topological: 45.6
  • Monoisotopic Mass: 241.05613515
  • Solubility: 26.4 [ug/mL]
  • Synonyms: 1628-29-1, 1-(10H-phenothiazin-10-yl)ethanone, 10-Acetylphenothiazine, Methyl phenothiazin-10-yl ketone, 10-Acetyl-10H-phenothiazine, P2H6XAV83R, 1-(10H-phenothiazin-10-yl)ethan-1-one, NSC-14724, DTXSID30167473, DTXCID7089964, dnvnqwuerfzasd-uhfffaoysa-n, inchi=1/c14h11nos/c1-10(16)15-11-6-2-4-8-13(11)17-14-9-5-3-7-12(14)15/h2-9h,1h, 1-phenothiazin-10-ylethanone, Phenothiazine, 10-acetyl-, 10H-PHENOTHIAZINE, 10-ACETYL-, Ethanone, 1-(10H-phenothiazin-10-yl)-, NSC14724, SR-01000809845, SR-01000809845-2, Ethanone,1-(10H-phenothiazin-10-yl)-, 1-Phenothiazin-10-yl-ethanone, EINECS 216-621-7, n-acetylphenothiazine, MFCD00022264, NSC 14724, 10-acetyl phenothiazine, CBMicro_018844, UNII-P2H6XAV83R, cid_74200, MLS001212169, SCHEMBL341905, 1-(10-phenothiazinyl)ethanone, SCHEMBL4778133, SCHEMBL6196289, SCHEMBL9658712, CHEMBL1437772, BDBM65851, 10-Acetyl-10H-phenothiazine #, HMS1681C22, HMS2825B20, CCG-6944, MSK180036, AKOS000282460, DS-9654, NCGC00245337-01, SMR000517771, BIM-0018708.P001, DS-010873, A3154, CS-0155045, NS00025315, ST45022158, C73127

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.

Safety and Hazards

GHS Hazard Statements

  • Not Classified
  • Reported as not meeting GHS hazard criteria by 1 of 1 companies. For more detailed information, please visit ECHA C&L website.

Hazard Classes and Categories

  • Not Classified

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.

Disclaimer

Intended Use & Restrictions

This product is sold exclusively for laboratory research, analytical testing, or non-commercial purposes.

  • Strictly prohibited: Resale, repackaging, or formulation into commercial products.
  • Not approved for human/animal use, diagnostics, or manufacturing (including pharmaceuticals, agrochemicals, or consumer goods).

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Certain molecules may be protected by active patents or regulatory restrictions.

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