Description
10-Phenylphenothiazine (CAS No. 7152-42-3) is a high-purity organic compound with the molecular formula C18H13NS, widely utilized in advanced chemical research and industrial applications. This heterocyclic aromatic compound features a phenothiazine core substituted with a phenyl group at the 10-position, offering unique electronic and photophysical properties. Our product is meticulously synthesized and purified to ensure exceptional quality, with rigorous analytical validation (HPLC, GC-MS, NMR) to guarantee ≥98% purity. Ideal for researchers in materials science, photochemistry, and organic electronics, 10-Phenylphenothiazine serves as a versatile building block for dyes, charge-transport materials, and redox-active ligands. Packaged under inert gas in amber glass vials to prevent degradation, it is supplied with comprehensive technical data, including spectral charts and safety documentation.
Properties
- CAS Number: 7152-42-3
- Complexity: 303
- IUPAC Name: 10-phenylphenothiazine
- InChI: InChI=1S/C18H13NS/c1-2-8-14(9-3-1)19-15-10-4-6-12-17(15)20-18-13-7-5-11-16(18)19/h1-13H
- InChI Key: WSEFYHOJDVVORU-UHFFFAOYSA-N
- Exact Mass: 275.07687059
- Molecular Formula: C18H13NS
- Molecular Weight: 275.4
- SMILES: C1=CC=C(C=C1)N2C3=CC=CC=C3SC4=CC=CC=C42
- Topological: 28.5
- Monoisotopic Mass: 275.07687059
- Synonyms: 10-phenyl-10h-phenothiazine, 10-Phenylphenothiazine, 7152-42-3, 10H-Phenothiazine, 10-phenyl-, Phenothiazine, 10-phenyl-, 10H-Phenothiazine, 10-phenyl- (9CI), n-phenylphenothiazine, BII1EYP5EW, MFCD00156238, NSC-23181, NSC 23181, BRN 0017325, C18H13NS, NSC23181, UNII-BII1EYP5EW, 4-27-00-01220 (Beilstein Handbook Reference), SCHEMBL342426, SCHEMBL712953, SCHEMBL712954, SCHEMBL7214767, SCHEMBL9776392, SCHEMBL21409893, DTXSID70221760, AKOS004907104, PHENYL-10H-PHENOTHIAZINE, 10-, DS-19168, SY271943, DB-215930, CS-0105611, P2470, D71026
Application
10-Phenylphenothiazine is employed as a key intermediate in the synthesis of organic semiconductors and hole-transport materials for OLEDs and photovoltaic devices. Its electron-donating properties make it valuable in photoredox catalysis and as a stabilizer in polymerization reactions. Researchers also utilize it to study radical scavenging mechanisms due to its persistent radical cation formation.
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