89333-28-8

Upstream product

• 540-63-6 ethane-1,2-dithiol 
• 72397-71-8 Dithiobenzoesaeure-carboxymethylester 
• 86878-59-3 dithiobenzoate de benzyl trimethyl ammonium 
• 106-93-4 ethylene dibromide 

Downstream Products

• 89333-33-5 meso-(R,S)-2,3-bis(methylthio)-2,3-diphenyl-1,4-dithiane 
• 89333-33-5 d,l-(R,R+S,S)-2,3-bis(methylthio)-2,3-diphenyl-1,4-dithiane 

Relevant academic research and scientific papers

Synthese de dithioesters par reaction des dithioacides ou de leurs sels (magnesiens mixtes ou d'ammonium quaternaire) sur les derives halogenes, les aldehydes et les epoxydes

In a previous paper we have shown that quaternary ammonium salts of dithiocarboxylic acids could substitute labile chlorine atoms of PVC without elimination of hydrochloric acid.This results demonstrated the high nucleophilic power associated with a low b

Electroreduction of Organic Compounds. 4. Electrochemical Reduction of Mono- and Bis-dithiobenzoate Esters in the Presence of Bi- or Monofunctional Electrophiles

Co-electroreduction of methyl dithiobenzoate (1a) and 1,3-dimesyloxypropane (5) in acetonitrile yields the tetrahydrodithiepine 6, whereas the thiirane 9 is formed from trimethylene-1,3-bis-dithiobenzoate (7a) and methyl iodide.The bis-thioacetals 8 are obtained, if 7a and its homologue 7b are electrolized together with methyl iodide; the heterocyclic bis-thioacetal 10 is formed from 7c as a mixture of the meso- and d,l-diastereomers in acetonitrile.