33758-38-2

Upstream product

• 463-71-8 thiophosgene 
• 106-54-7 p-Chlorothiophenol 

Downstream Products

• 26132-86-5 Dithiocarbonic acid O-[5-chloro-2-(3,4-dichloro-phenoxy)-phenyl] ester S-(4-chloro-phenyl) ester 
• 25995-64-6 Dithiocarbonic acid O-[5-chloro-2-(2,4-dichloro-phenoxy)-phenyl] ester S-(4-chloro-phenyl) ester 
• 53271-57-1 S,S'-Bis-(4-chlorphenyl)-trithiocarbonat-S,S-dioxid 
• 25995-66-8 Dithiocarbonic acid S-(4-chloro-phenyl) ester O-(5-chloro-2-p-tolyloxy-phenyl) ester 
• 25995-67-9 Dithiocarbonic acid O-[5-chloro-2-(2,4-dibromo-phenoxy)-phenyl] ester S-(4-chloro-phenyl) ester 
• 27760-25-4 O-(4-nitrophenyl) S‐(4‐chlorophenyl) dithiocarbonate 
• 163065-00-7 C₁₄H₁₁Cl₃O₂S₃ 
• 1523313-43-0 C₁₄H₁₁ClOS₃ 
• 1523313-30-5 p-chlorophenyl p-tolyl trithiocarbonate 
• 1523313-45-2 C₁₃H₆Cl₄OS₃ 
• 1523313-33-8 p-chlorophenyl 2,4,5-trichlorophenyl trithiocarbonate 
• 163064-96-8 C₁₄H₁₁ClO₂S₃ 

Relevant academic research and scientific papers

Synthesis and Application of Chlorodithiocarbonates, Thionothiocarbonates, and Thionoselenocarbonates in Radical Chain Reactions

Thionothiocarbonates as well as the corresponding selenium compounds are good radiophillic starting materials for the efficient radical chain reactions of alcohols.