86211-04-3

Upstream product

• 1212-08-4 S-Phenyl benzenethiosulfonate 
• 201230-82-2 carbon monoxide 
• 86210-96-0 ((Z)-1-Chloro-tridec-1-enylsulfanyl)-benzene 
• 108-98-5 thiophenol 

Relevant academic research and scientific papers

Tin-free radical carbonylation: Thiol ester synthesis using alkyl allyl sulfone precursors, phenyl benzenethiosulfonate, and CO

(Chemical Equation Presented) Remove contents from tin ... Thiol esters have been successfully synthesized through tin-free radical carbonylation (see scheme; V-40 = initiator). This approach can be further extended to sequential radical reactions involving cyclization, carbonylation, and trapping of acyl radicals by phenyl benzenethiosulfonate.

A HIGHLY CONVENIENT PROCEDURE FOR THE HYDROLYSIS OF TERMINAL PHENYL VINYL SULFIDES

Terminal vinyl and chlorovinyl sulfides are hydrolyzed by 70percent perchloric acid-thiophenol in benzene to the corresponding diphenyl thioacetals and thioesters in good yields.