4-Chlorothiophenol undergoes oxidative coupling catalyzed by iron(III)-tetra phenyl prophyrin to form disulfides.4-Chlorothiophenol was used to modify poly(vinyl chloride) and to synthesize poly(vinyl chloride) with halogen groups. Reactant involved in: . Oxidation to disulfides using cobalt-salen catalysts and air oxidizing agents . Thiourea-catalyzed sulfa-Michael addition to acryloyloxazolidinones . Pummerer-type cyclization . C-H Activation and C-S cross-coupling with heterocycles . Allylic sulfenylation with allylic carbonates . Lewis acid-catalyzed electrophilic ring-opening reactions of 2-aryl-3,4-dihydropyrans 4-Chlorothiophenol undergoes oxidative coupling catalyzed by iron(III)-tetra phenyl prophyrin to form disulfides. 4-Chlorothiophenol was used to modify poly(vinyl chloride) and to synthesize poly(vinyl chloride) with halogen groups. Reactant involved in: . Oxidation to disulfides using cobalt-salen catalysts and air oxidizing agents . Thiourea-catalyzed sulfa-Michael addition to acryloyloxazolidinones . Pummerer-type cyclization . C-H Activation and C-S cross-coupling with heterocycles . Allylic sulfenylation with allylic carbonates . Lewis acid-catalyzed electrophilic ring-opening reactions of 2-aryl-3,4-dihydropyrans