Cas no 1910-85-6 (1-Chloro-10H-phenothiazine)

1-Chloro-10H-phenothiazine structure
1-Chloro-10H-phenothiazine structure
Product Name:1-Chloro-10H-phenothiazine
CAS No:1910-85-6
MF:C12H8ClNS
MW:233.716620445251
MDL:MFCD18447826
CID:229961
PubChem ID:350922
Update Time:2025-04-19

1-Chloro-10H-phenothiazine Chemical and Physical Properties

Names and Identifiers

    • 10H-Phenothiazine,1-chloro-
    • 1-chloro-10H-phenothiazine
    • 1-Chlorophenothiazin
    • 1-chloro-phenothiazine
    • 1-CHLOROPHENOTHIAZINE
    • 1-Chlor-phenothiazin
    • 2-Chlor-phenothiazin
    • AC1L6XA5
    • AG-E-39524
    • CTK4E0576
    • NSC516775
    • SureCN560873
    • 10H-Phenothiazine, chloro-
    • phenothiazine chloride
    • AK386984
    • MFCD18447826
    • AKOS027379023
    • A880390
    • 10H-Phenothiazine, 1-chloro-
    • DTXSID60325741
    • SCHEMBL560873
    • DS-12980
    • BAA91085
    • 1910-85-6
    • NSC-516775
    • CS-W018471
    • TUZVTRCMDIUEBE-UHFFFAOYSA-N
    • NSC 516775
    • A11135
    • DB-103191
    • 1-Chloro-10H-phenothiazine
    • MDL: MFCD18447826
    • Inchi: 1S/C12H8ClNS/c13-8-4-3-7-11-12(8)14-9-5-1-2-6-10(9)15-11/h1-7,14H
    • InChI Key: TUZVTRCMDIUEBE-UHFFFAOYSA-N
    • SMILES: ClC1=CC=CC2=C1NC1C=CC=CC=1S2

Computed Properties

  • Exact Mass: 233.00674
  • Monoisotopic Mass: 233.007
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 0
  • Complexity: 236
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 37.3
  • XLogP3: 4.2

Experimental Properties

  • Density: 1.346±0.06 g/cm3 (20 oC 760 Torr),
  • Melting Point: 96.2-96.7 oC
  • Boiling Point: 392.3oC at 760mmHg
  • Flash Point: 191.1oC
  • Refractive Index: 1.68
  • Solubility: Insuluble (9.3E-4 g/L) (25 oC),
  • PSA: 12.03
  • LogP: 4.68620

1-Chloro-10H-phenothiazine Pricemore >>

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1-Chloro-10H-phenothiazine Related Literature

  • 1. 1,2-Didehydrophenothiazines: preparation of 1-alkyl and 1-aryl-substituted phenothiazines by lithium-directed alkylation
    Anders Hallberg,Philip Dunbar,Nalukui Mwisya Hintermeister,Arne Svensson,Arnold R. Martin J. Chem. Soc. Perkin Trans. 1 1985 969
  • 2. Reduction of nitro- and nitroso-compounds by tervalent phosphorus reagents. Part IX. The ‘blocked ortho’ effect in reactions of 2,6-di-substituted aryl 2-nitrophenyl and 2,6-disubstituted aryl 2-azidophenyl sulphides: a new series of nitrene-induced aromatic rearrangements
    J. I. G. Cadogan,S. Kulik J. Chem. Soc. C 1971 2621
  • 3. Nitrene-induced cyclisations accompanied by rearrangement in thermolyses of aryl 2-azidophenyl sulphones: a note on quantitative high-speed liquid chromatographic analysis of substituted phenothiazine 5,5-dioxides
    J. I. G. Cadogan,John N. Done,George Lunn,Peter K. K. Lim J. Chem. Soc. Perkin Trans. 1 1976 1749
  • 4. Chapter 5. Arynes, carbenes, nitrenes, and related species
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