66437-74-9

Upstream product

• 60565-57-3 N-<1,3,5>-Trithian-1-ylidene-4-methylbenzenesulfonamide 
• 108-95-2 phenol 

Downstream Products

• 43079-11-4 phenylsulfanyl-[1,3,5]trithiane 
• 34119-70-5 2-(p-Dimethylaminophenyl)-s-trithian 
• 59338-72-6 2-(p-Hydroxyphenyl)-1,3,5-trithian 
• 81259-25-8 1,5-Bis-(2-trithianyl)-1,3,5-trithiapentan 
• 16737-44-3 Orthoameisensaeuretriphenylester 
• 81259-29-2 1-(Bis-phenoxymethyl)-5-(2-trithianyl)-1,3,5-trithiapentan 
• 81259-27-0 1-Mercapto-4-(2-trithianyl)-2,4-dithiabutan 
• 81259-28-1 1-Formyl-5-(2-trithianyl)-1,3,5-trithiapentan 
• 81259-36-1 2-Hydroxy-3-cyan-4-phenyl-5-(2-trithianyl)-thiophen 

Relevant academic research and scientific papers

Synthesis and Reactions of 2-Aryloxy-s-trithianes

2-Aryloxy-s-trithianes 4 had been prepared from 1-tosyl-imino-1-SIV-1,3,5-trithiane and phenolates. - By self-condensation of 4 1,5-bis-(trithianyl)-1,3,5-trithiapentane 5 and triphenylorthoformate 7 are formed, accompanied by further products, which had been isolated in pure state and identified unambiguously by H-n.m.r. and mass-spectra.In the presence of acids the 2-aryloxy-s-trithianes 4 react with nucleophilic aromatic compounds such as phenoles, N,N-dimethylaniline, pyrrole, indole, and thiophenes to give the C-trithianylated products.With mercaptanes 2-alkylthio-s-trithianes are formed.