137897-99-5

Usage

Uses

Since the provided materials do not specify any particular applications for 3,3',5,5'-tetrachlorodiphenyl disulfide, it is not possible to list its uses based on the given information. Further research would be required to determine its potential applications in various industries.

Upstream product

• 705-21-5 3,5-dichlorobenzensulfonyl chloride 
• 17231-94-6 3,5-dichlorothiophenol 
• 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 
• 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 
• 1429474-44-1 3-((3,5-dichlorophenyl)thio)-1H-indole-2-carboxylic acid 
• 1429474-43-0 3-((3,5-dichlorophenyl)thio)-6-ethyl-1H-indole-2-carboxylic acid 
• 1429474-18-9 3-(3-((3,5-dichlorophenyl)thio)-6-methyl-1H-indol-2-yl)propanoic acid 
• 1631147-09-5 2-(1,3-diazepan-2-ylidene)-2-((3,5-dichlorophenyl)thio)-1-phenylethan-1-one 
• 1631146-89-8 2-((3,5-dichlorophenyl)thio)-1-phenyl-2-(tetrahydropyrimidin-2(1H)-ylidene)ethanone 

Relevant academic research and scientific papers

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.

Dithioates of Meldrum's acid, dimedone, and barbituric acid, novel sulfur transfer reagents for the one-pot copper-catalyzed conversion of aryl iodides into diaryl disulfides

We report herein the first application of CH-acid dithioates as sulfur transfer reagents. A new route for the synthesis of diaryldisulfides using the copper-catalyzed conversion of aryl iodides in the presence of Melderum's acid, dimedone or barbituric acid dithioates is discussed.

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.

Synthesis of carbonates and related compounds from carbon dioxide via methanesulfonyl carbonates

Carbonate anions resulting from reaction of primary or secondary alcohols with carbon dioxide, when added to methanesulfonic anhydride in cooled acetonitrile solution, yield methanesulfonyl carbonates, a new class of synthetic intermediate. Base-mediated reaction of the methanesulfonyl carbonates with alcohols, thiols, and amines yields carbonates, thiocarbonates, and carbamates, respectively. Overall yields for the three steps vary from 19% to 42%.