137897-99-5

Basic information

• Product Name: 3,3',5,5'-TETRACHLORODIPHENYL DISULFIDE
• Synonyms: 3,3',5,5'-TETRACHLORODIPHENYL DISULFIDE;BIS(3,5-DICHLOROPHENYL) DISULFIDE;BIS(3,5-DICHLOROPHENYL)DISULPHIDE;3,3,5,5-TETRACHLORODIPHENYL DISULFIDE 98+%;3,3',5,5'-TETRACHLOR;1,2-Bis(3,5-dichlorophenyl)disulfane
• CAS NO: 137897-99-5
• Molecular Formula: C₁₂H₆Cl₄S₂
• Molecular Weight: 356.12
• Product Categories: Organic Building Blocks;Sulfides/Disulfides;Sulfur Compounds;Building Blocks;Chemical Synthesis;Organic Building Blocks;Sulfur Compounds
• Mol File: 137897-99-5.mol
• Article Data: 5

Chemical Properties

• Melting Point: 66-69 °C(lit.)
• Boiling Point: 429.733 °C at 760 mmHg
• Flash Point: 197.066 °C
• Appearance: /
• Density: 1.599 g/cm³
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: almost transparency in Toluene
• CAS DataBase Reference: 3,3',5,5'-TETRACHLORODIPHENYL DISULFIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3',5,5'-TETRACHLORODIPHENYL DISULFIDE(137897-99-5)
• EPA Substance Registry System: 3,3',5,5'-TETRACHLORODIPHENYL DISULFIDE(137897-99-5)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 137897-99-5(Hazardous Substances Data)

Usage

General Description

3,3',5,5'-Tetrachlorodiphenyl disulfide is a synthetic organic compound that belongs to the class of chemicals known as dichlorobenzenes. 3,3',5,5'-TETRACHLORODIPHENYL DISULFIDE is characterized by the presence of two benzene rings, each of which is substituted with two chlorine atoms. It also contains a disulfide bond, a functional group composed of two sulfur atoms. Due to its chemical structure, it exhibits various physical and chemical properties, including high thermal stability and resistance to oxidative degradation. Unlike other halogenated organic compounds, 3,3',5,5'-tetrachlorodiphenyl disulfide is less persistent in the environment owing to the presence of its disulfide bond, making it relatively easier to degrade and remove. This chemical is not widely used and its toxicity and potential ecological effects are not well-studied.

Upstream product

• 17231-94-6 3,5-dichlorothiophenol 
• 705-21-5 3,5-dichlorobenzensulfonyl chloride 
• 3032-81-3 3,5-dichloroiodobenzene 

Downstream Products

• 198421-53-3 3S-(3,5-dichlorophenylthio)-2S-isobutylbutan-1,4-dioic acid 4-tert-butyl ester 
• 198421-52-2 N²-[3S-(3,5-dichlorophenylthio)-4-hydroxy-2S-isobutylsuccinyl]-L-tert-leucine-N¹-methylamide 
• 198421-55-5 N²-[4-tert-butyloxy-3S-(3,5-dichlorophenylthio)-2S-isobutylsuccinyl]-L-tert-leucine-N¹-methylamide 
• 125056-76-0 6-<(3,5-dichlorophenyl)thio>-1-<(2-hydroxyethoxy)methyl>thymine 
• 137897-93-9 6-<(3,5-dichlorophenyl)thio>-5-ethyl-1-<(2-hydroxyethoxy)methyl>uracil 
• 137897-90-6 6-<(3,5-dichlorophenyl)thio>-5-ethyl-1-<(2-hydroxyethoxy)methyl>-2-thiouracil 
• 74282-78-3 3,5-dichlorobenzenesulfenyl chloride 
• 143535-34-6 1-(dimethylsulfamoyl)-4-chloro-5-(3,5-dichlorophenylthio)pyrazole 
• 705-21-5 3,5-dichlorobenzensulfonyl chloride 
• 1429474-12-3 3-((3,5-dichlorophenyl)thio)-6-methyl-1H-indole-2-carboxylate 
• 1429474-13-4 3-((3,5-dichlorophenyl)thio)-N,6-dimethyl-1H-indole-2-carboxamide 
• 1429474-23-6 4-(3-((3,5-dichlorophenyl)thio)-6-methyl-1H-indol-2-yl)butanoic acid 
• 1429474-25-8 2-(3-((3,5-dichlorophenyl)thio)-6-methyl-1H-indol-2-yl)acetic acid 
• 1429474-08-7 3-((3,5-dichlorophenyl)thio)-6-methyl-1H-indole-2-carboxylic acid 

Relevant articles and documents

Green Aerobic Oxidation of Thiols to Disulfides by Flavin-Iodine Coupled Organocatalysis

Coupled catalysis using a riboflavin-derived organocatalyst and molecular iodine successfully promoted the aerobic oxidation of thiols to disulfides under metal-free mild conditions. The activation of molecular oxygen occurred smoothly at room temperature through the transfer of electrons from the iodine catalyst to the biomimetic flavin catalyst, forming the basis for a green oxidative synthesis of disulfides from thiols.

Synthesis of aryl perfluoroalkyl sulfides from aromatic disulfides

Thermolysis of xenon(II) bis(perfluoroalkanecarboxylates) in the presence of diaryl disulfides occurs through the S-S bond cleavage to form dihalo-, halonitro-, and halodinitrophenyl perfluoroalkyl sulfides. The latter type of compounds was obtained for the first time. The main side process is the perfluoroalkylation of the aromatic ring.

Process for producing bishalophenyl disulfide

This invention is directed to a process for producing a bishalophenyl disulfide, chracterized by reacting a halothiophenol with an alkali metal hydroxide to obtain an alkali metal halothiophenolate and subsequently converting the halothiophenolate into a disulfide with an oxidizing agent in the presence of a mineral acid. By the process, a bishalophenyl disulfide having a high purity can be industrially produced in high yield.