Introduction：Basic information about 2-Chlorophenothiazine CAS 92-39-7, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
2-Chlorophenothiazine Basic information
| Product Name: | 2-Chlorophenothiazine |
| Synonyms: | 2-CHLOROTHIODIPHENYLAMINE;2-CHLOROPHENOTHIAZINE;TIMTEC-BB SBB003255;2-Chlorophenothiazine, 98%+;3-CHLOROPHENOTHIAZINE;10H-Phenothiazine,2-chloro-;Chlorophenothiazine;CyaMeMazine Chloro IMpurity |
| CAS: | 92-39-7 |
| MF: | C12H8ClNS |
| MW: | 233.72 |
| EINECS: | 202-152-5 |
| Product Categories: | Sulphur Derivatives;Intermediates & Fine Chemicals;Metabolites & Impurities;Pharmaceuticals;Sulfur & Selenium Compounds;Metabolites & Impurities, Pharmaceuticals, Intermediates & Fine Chemicals, Sulfur & Selenium Compounds;API Intermediate |
| Mol File: | 92-39-7.mol |
|
2-Chlorophenothiazine Chemical Properties
| Melting point | 195-200 °C (lit.) |
| Boiling point | 395.7±31.0 °C(Predicted) |
| density | 1.2350 (rough estimate) |
| refractive index | 1.6100 (estimate) |
| storage temp. | 2-8°C |
| solubility | DMSO (Slightly), Methanol (Slightly, Sonicated) |
| pka | -2.28±0.20(Predicted) |
| form | crystals |
| color | Pale Beige to Beige |
| BRN | 176587 |
| InChI | InChI=1S/C12H8ClNS/c13-8-5-6-12-10(7-8)14-9-3-1-2-4-11(9)15-12/h1-7,14H |
| InChIKey | KFZGLJSYQXZIGP-UHFFFAOYSA-N |
| SMILES | C1=C2C(SC3=C(N2)C=CC=C3)=CC=C1Cl |
| LogP | 3.28 |
| CAS DataBase Reference | 92-39-7(CAS DataBase Reference) |
| EPA Substance Registry System | 10H-Phenothiazine, 2-chloro- (92-39-7) |
Safety Information
| Hazard Codes | Xi |
| Risk Statements | 36/37/38 |
| Safety Statements | 26-36-37/39 |
| WGK Germany | 3 |
| RTECS | SN7580000 |
| TSCA | TSCA listed |
| HS Code | 2934300000 |
| Storage Class | 11 - Combustible Solids |
| Hazard Classifications | Skin Sens. 1 |
2-Chlorophenothiazine Usage And Synthesis
| Chemical Properties | GREYISH TO SLIGHTLY GREEN OR BROWNISH POWDER |
| Uses | Metabolite of Chloropromazine |
| Uses | 2-Chlorophenothiazine may be used as starting reagent for the synthesis of N-(10H-phenothiazin-1-yl) benzene sulphonamide. |
| General Description | 2-Chlorophenothiazine is an methylene blue (MB) derivative. Transient resonance Raman and absorption spectra of the lowest excited triplet states T1 and the cation radicals of 2-chlorophenothiazine have been investigated. Molecular semiconductors based on the 1:1 charge-transfer complexes of 2-chlorophenothiazine with 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ) have been investigated by X-ray powder diffraction. |
2-Chlorophenothiazine Preparation Products And Raw materials
| Raw materials | Hydrogen Sulfide-->3-CHLORODIPHENYLAMINE-->Acetamide, N-(5-chloro-2-mercaptophenyl)--->acetamide, N-(2-mercaptophenyl)--->Ethanethioic acid, S-[2-(acetylamino)-4-chlorophenyl] ester-->3-CHLOROCYCLOHEXAN-1-ONE-->3-chloro-10H-phenothiazine-->Ethanethioic acid,S-[2-(acetylamino)phenyl] ester-->2-AMINO-4-CHLOROTHIOPHENOL-->5-CHLORO-2-IODOANILINE-->2-Bromo-4-chloro-1-iodobenzene |
| Preparation Products | Chlorpromazine hydrochloride-->PERPHENAZINE |
