17046-97-8

Basic information

• Product Name: S-(4-nitrophenyl) 4-methylbenzenesulfonothioate
• Synonyms: Toluene-4-thiosulfonic acid, S-(4-nitro-phenyl) ester
• CAS NO: 17046-97-8
• Molecular Formula: C₁₃H₁₁NO₄S₂
• Molecular Weight: 309.3607
• Mol File: 17046-97-8.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 499°C at 760 mmHg
• Flash Point: 255.6°C
• Density: 1.46g/cm³
• Vapor Pressure: 1.33E-09mmHg at 25°C
• Refractive Index: 1.668
• CAS DataBase Reference: S-(4-nitrophenyl) 4-methylbenzenesulfonothioate(CAS DataBase Reference)
• NIST Chemistry Reference: S-(4-nitrophenyl) 4-methylbenzenesulfonothioate(17046-97-8)
• EPA Substance Registry System: S-(4-nitrophenyl) 4-methylbenzenesulfonothioate(17046-97-8)

Safety Data

• Hazardous Substances Data: 17046-97-8(Hazardous Substances Data)

Upstream product

• 63296-21-9 methyl 4-nitrophenyl disulphide 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 3753-27-3 sodium 4-methylbenzenesulfonothioate 
• 1849-36-1 para-nitrobenzenethiol 
• 459-44-9 4-methylbenzenediazonium tetrafluoroborate 
• 1576-35-8 toluene-4-sulfonic acid hydrazide 
• 98-59-9 p-toluenesulfonyl chloride 
• 98-74-8 4-Nitrobenzenesulfonyl chloride 
• 100-32-3 di(p-nitrophenyl) disulfide 
• 17796-89-3 1-[(4-nitrophenyl)sulfanyl]pyrrolidine-2,5-dione 
• 937-32-6 4-nitrobenzenesulfenyl chloride 
• 28519-50-8 potassium thiotosylate 
• 14756-51-5 4-nitrophenyl p-tolyl disulfide 

Downstream Products

• 39248-99-2 S-(4-nitrophenyl) 4-methylbenzothioate 
• 60094-81-7 1-[(4-nitrophenyl)thio]piperidine 

Relevant articles and documents

Organocatalytic Transformation of Aldehydes to Thioesters with Visible Light

A metal- and oxidant-free catalytic method for accessing structurally diverse thioesters from readily accessible, widespread aldehydes, is described. A strategy of a simple organic 9,10-phenanthrenequinone-promoted hydrogen atom transfer (HAT) with visible light was successfully implemented to selectively generate acyl radicals without inducing crossover reactivity of thioester products. The preparative power of the method was demonstrated by broad substrate scope and wide functional group tolerance, and enabled the late-stage modification of complex structures, which are difficult to achieve with the existing protocols.

Method for synthesizing thiosulfonate compounds on the basis of strategy of SO2 insertion

The invention relates to a method for synthesizing thiosulfonate compounds on the basis of strategy of SO2 insertion. The method includes: performing a reaction in the presence of nitrogen gas and atcertain temperature to prepare the thiosulfonate compoun

Tunable and Practical Synthesis of Thiosulfonates and Disulfides from Sulfonyl Chlorides in the Presence of Tetrabutylammonium Iodide

A tunable and practical synthesis of electrophilic sulfenylating reagents, thiosulfonates and disulfides, from inexpensive and easily available sulfonyl chlorides, has been developed. By appropriate choice of solvents, the reaction of sulfonyl chlorides and tetrabutylammonium iodide gave the target products in good to excellent yields, respectively. These transformations probably proceed through a reducing–coupling pathway. (Figure presented.).