96097-67-5

Basic information

• Product Name: S-(2-methylphenyl) benzenesulfonothioate
• Synonyms: S-(2-methylphenyl) benzenesulfonothioate
• CAS NO: 96097-67-5
• Molecular Weight: 264.369
• Mol File: 96097-67-5.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: S-(2-methylphenyl) benzenesulfonothioate(CAS DataBase Reference)
• NIST Chemistry Reference: S-(2-methylphenyl) benzenesulfonothioate(96097-67-5)
• EPA Substance Registry System: S-(2-methylphenyl) benzenesulfonothioate(96097-67-5)

Safety Data

• Hazardous Substances Data: 96097-67-5(Hazardous Substances Data)

Upstream product

• 83878-24-4 phenyl-o-tolyl disulfide 
• 873-55-2 sodium benzenesulfonate 
• 4032-80-8 bis(2-methylphenyl)disulfide 
• 1887-29-2 sodium phenylthiosulfonate 
• 80-17-1 benzenesufonyl hydrazide 
• 137-06-4 2-thiocresol 
• 14664-64-3 2-methylbenzenesulfenyl chloride 
• 618-41-7 Benzenesulfinic acid 

Downstream Products

• 59693-92-4 cyclohexyl 2-methylphenyl sulfide 

Relevant articles and documents

Visible-Light-Induced Radical Cascade Reaction of 1-Allyl-2-ethynylbenzoimidazoles with Thiosulfonates to Assemble Thiosulfonylated Pyrrolo[1,2-a]benzimidazoles

A visible-light-induced radical domino reaction of 1-allyl-2-ethynylbenzoimidazoles with thiosulfonates was developed, which generated the thiosulfonylated pyrrolo[1,2-a]benzimidazoles in moderate to good yields. This reaction proceeded under transition-metal-free conditions with good functional group tolerance and high regioselectivity. The possible pathway involved thiosulfonates were activated through the energy transfer route promoted by photocatalysis.

Nickel-Catalyzed Defluorinative Reductive Cross-Coupling Reaction of gem-Difluoroalkenes with Thiosulfonate or Selenium Sulfonate

A nickel-catalyzed defluorinative reductive cross-coupling of gem-difluoroalkenes with thiosulfonate or selenosulfonates is described. The reaction involves the formation of thiolated or selenylated monofluoroolefins via regioselective C-F bond cleavage and C-S or C-Se bond formation and features easily available substrates, mild reaction conditions, and high E-selectivity. One of the derivatives by further cross coupling with PhMgBr exhibited an aggregation-induced emission enhancement effect.

Synthesis method of thiosulfonate compound

The invention belongs to the field of organic synthesis, and particularly relates to a synthesis method of a thiosulfonate compound. The invention provides the synthesis method of the thiosulfonate compound. The method comprises the following steps that methanesulfonohydrazide compounds, thiophenol compounds, oxidizing agents and catalysts are dissolved into a solvent for reaction; purification isperformed to obtain the thiosulfonate compound; oxidizing agents are any one kind or several kinds of materials from tertiary butanol peroxide and catalysts are sodium iodide, potassium iodide, ammonium iodide, iodine element and tetrabutylammonium iodide. Through experiment testing, the thiosulfonate compound prepared by the technical scheme provided by the invention has the advantages that no side reaction occurs; the yield can reach 84 to 100 percent; the conversion rate is high; meanwhile, the used catalysts and catalysts are environment-friendly compounds; the environment pollution cannot be caused; the reaction temperature is low; the method is suitable for industrial mass popularization. The defects that in the prior art, the damage to the environment in the asymmetric thiosulfonates synthesis process is great, and the application to industrial production cannot be realized are overcome.