1910-85-6

Basic information

• Product Name: 1-Chlorophenothiazine
• Synonyms: 1-Chlorophenothiazine;1-chloro-10H-phenothiazine
• CAS NO: 1910-85-6
• Molecular Formula: C₁₂H₈ClNS
• Molecular Weight: 233.71662
• Mol File: 1910-85-6.mol
• Article Data: 5

Chemical Properties

• Melting Point: 92 °C
• Boiling Point: 392.3°Cat760mmHg
• Flash Point: 191.1°C
• Appearance: /
• Density: 1.346g/cm³
• Vapor Pressure: 2.31E-06mmHg at 25°C
• Refractive Index: 1.68
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• PKA: -2.98±0.20(Predicted)
• CAS DataBase Reference: 1-Chlorophenothiazine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Chlorophenothiazine(1910-85-6)
• EPA Substance Registry System: 1-Chlorophenothiazine(1910-85-6)

Safety Data

• Hazardous Substances Data: 1910-85-6(Hazardous Substances Data)

Usage

Uses

1-Chlorophenothiazine is used in electronic structure and physical-chemical properties relationship for phenothiazine derivatives by quantum chemical calculations.

InChI:InChI=1/C12H8ClNS/c13-8-4-3-7-11-12(8)14-9-5-1-2-6-10(9)15-11/h1-7,14H

Upstream product

• 2401-21-0 1,2-Dichloro-3-iodobenzene 
• 1204-55-3 thioacetic acid S-(2-acetylamino-phenyl)ester 
• 533-17-5 N-(2-chlorophenyl)acetamide 
• 108-86-1 bromobenzene 
• 88-73-3 2-Chloronitrobenzene 
• 93075-13-9 2-Chloro-6-(2-nitro-phenylsulfanyl)-phenylamine 
• 40925-72-2 2-amino-3-chlorobenzenethiol 
• 93091-66-8 N-[2-Chloro-6-(2-nitro-phenylsulfanyl)-phenyl]-formamide 
• 33253-05-3 1,3-dichloro-2-(2-nitro-phenylsulfanyl)-benzene 
• 33253-01-9 (2-chloro-phenyl)-(2-nitro-phenyl)-sulfane 
• 92-84-2 10H-phenothiazine 
• 1205-40-9 N-phenyl-2-chloroaniline 

Downstream Products

• 135358-84-8 10-benzyl-1-chlorophenothiazine 

Relevant articles and documents

Transition-metal-free synthesis of phenothiazines from S-2-acetamidophenyl ethanethioate and ortho-dihaloarenes

An efficient cesium carbonate-mediated synthesis of phenothiazine derivatives from S-2-acetamidophenyl ethanethioates and ortho-dihaloarenes has been developed. This protocol affords an efficient approach for the construction of phenothiazine derivatives without the need of transition-metal catalyst or ligand. A plausible mechanism is proposed.

Studies on phenothiazines. Part II. [1]. Synthesis and spectral studies of substituted 1- chloro/methyl/nitrophenothiazines

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Free radicals of phenothiazine and related compounds. IV. Phenothiazinyl- and diphenothiazine-copper complexes as intermediates and products in the interaction of phenothiazines with copper(II) halides

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