3808-87-5

Basic information

• Product Name: BIS(2,4,5-TRICHLOROPHENYL) DISULFIDE
• Synonyms: 2,4,5-TRICHLOROPHENYL DISULFIDE;BIS(2,4,5-TRICHLOROPHENYL) DISULFIDE;BIS(2,4,5-TRICHLOROPHENYL) DISULPHIDE;DI(2,4,5-TRICHLOROPHENYL) DISULFIDE;2,2,4,4,5,5-Hexachlorophenyl disulphide~2,4,5-Trichlorophenyl disulphide;2,4,5-trichlorophenyl disulphide;2,4,5-TRICHLOROPHENYL DISULFIDE 98%;Bis(2,4,5-trichlorophenyl) persulfide
• CAS NO: 3808-87-5
• Molecular Formula: C₁₂H₄Cl₆S₂
• Molecular Weight: 425.01
• EINECS: 223-279-2
• Mol File: 3808-87-5.mol
• Article Data: 5

Chemical Properties

• Melting Point: 140-144 °C(lit.)
• Boiling Point: 460.9°Cat760mmHg
• Flash Point: 213.2°C
• Appearance: /
• Density: 1.6505 (estimate)
• Vapor Pressure: 3.08E-08mmHg at 25°C
• Refractive Index: 1.718
• CAS DataBase Reference: BIS(2,4,5-TRICHLOROPHENYL) DISULFIDE(CAS DataBase Reference)
• NIST Chemistry Reference: BIS(2,4,5-TRICHLOROPHENYL) DISULFIDE(3808-87-5)
• EPA Substance Registry System: BIS(2,4,5-TRICHLOROPHENYL) DISULFIDE(3808-87-5)

Safety Data

• Safety Statements: S24/25:Avoid contact with skin and eyes.
• WGK Germany: 3
• Hazardous Substances Data: 3808-87-5(Hazardous Substances Data)

Usage

General Description

Bis(2,4,5-trichlorophenyl) disulfide is a chemical compound composed of two phenyl groups, each containing three chlorine atoms, bonded to a sulfur atom. It is used as a pesticide and fungicide due to its strong antimicrobial and antifungal properties. This chemical is classified as a chlorinated aromatic compound and has been shown to have toxic effects on aquatic organisms. It is also considered to be a persistent organic pollutant and is subject to international regulations and restrictions on its use and production due to its potential to bioaccumulate and harm the environment. Bis(2,4,5-trichlorophenyl) disulfide's structure and properties make it important for understanding its potential impact on human health and the environment.

InChI:InChI=1/C12H4Cl6S2/c13-5-1-9(17)11(3-7(5)15)19-20-12-4-8(16)6(14)2-10(12)18/h1-4H

Upstream product

• 15945-07-0 2,4,5-trichlorobenzensulfonyl chloride 
• 24082-44-8 bis-(2,4,5-trichloro-phenyl)-trisulfide 
• 636-30-6 2,4,5-trichloroaniline 
• 88-67-5 2-Iodobenzoic acid 
• 3773-14-6 2,4,5-trichlorothiophenol 
• 10439-21-1 2,4,5-trichloro-benzenesulfinic acid 
• 62726-90-3 2,4,5-trichlorobenzenesulfenyl chloride 
• 594-27-4 tetramethylstannane 
• 120-82-1 1,2,4-Trichlorobenzene 

Downstream Products

• 102105-06-6 N-(diphenylmethylene)-2,4,5-trichlorophenylsulfenamide 
• 102105-04-4 N-(dibenzocyclohepten-5-ylidene)-2,4,5-trichlorophenylsulfenamide 
• 3773-14-6 2,4,5-trichlorothiophenol 
• 4184-55-8 Monothiophosphorsaeure-O,O-dimethylester-S-<2,4,5-trichlor-phenylester> 
• 62726-90-3 2,4,5-trichlorobenzenesulfenyl chloride 
• 247237-68-9 4-hydroxy-3-(2,4,5-trichlorophenylthio)-2(1H)-quinolone 
• 247237-66-7 4-hydroxy-1-phenyl-3-(2,4,5-trichlorophenylthio)-2(1H)-quinolone 
• 247237-75-8 4-hydroxy-1-phenyl-3-(2,4,5-trichlorophenylthio)-5,6,7,8-tetrahydro-2(1H)-quinolone 
• 247237-97-4 4-hydroxy-3-(2,4,5-trichlorophenylsulfonyl)-1-phenyl-5,6,7,8-tetrahydro-2(1H)-quinolone 
• 4163-78-4 2,4,5-trichloromethylthiobenzene 
• 4163-80-8 2,4,5-trichlorophenyl methyl sulfone 
• 264926-02-5 [2,4,5-Cl₃(C₆H₂)SSnMe₃] 
• 15945-07-0 2,4,5-trichlorobenzensulfonyl chloride 
• 1429474-47-4 4-methyl-3-((2,4,5-trichlorophenyl)thio)-1H-indole-2-carboxylic acid 

Relevant articles and documents

Synthesis of Disulfides from the Palladium(0)-Catalyzed Reactions of Sulfenyl Halides and Organostannanes

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Thioxanthene derivatives of pharmacological interest: 1,2,4-trichloro and 2,4,5,6-tetrachloro derivatives of 9-(3-dimethylaminopropylidene)thioxanthene

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REACTION OF N,N'-THIONYLDIIMIDAZOLE WITH THIOLS: A SULFUR TRANSFER REACTION

Reaction of N,N'-thionyldiimidazole with thiols effects the formation of disulfides and trisulfides.These results are rationalized by assuming that the thiols react with N,N'-thionyldiimidazole to produce the disulfides and N,N'-thiobisimidazole which subsequently reacts with the starting thiols to give the trisulfides.