38348-26-4Relevant academic research and scientific papers
1,3,5-Trithianes and sulfur monochloride/sodium sulfide: an alternative route to 3,5-disubstituted 1,2,4-trithiolanes
Tanini, Damiano,Trapani, Francesca,Capperucci, Antonella
, p. 635 - 644 (2020)
Treatment of substituted 1,3,5-trithianes with S2Cl2 and Na2S under mild conditions provides 3,5-disubstituted 1,2,4-trithiolanes, as mixture of diastereoisomers.
DISUBSTITUTED TETRATHIANES AS FRAGRANCES OR FLAVOURINGS
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Page/Page column 20; 21, (2008/06/13)
The use (i) of a compound of formula 2 wherein R3 and R4 independently of one another represent a C2-C4-alkyl or -alkenyl radical or (ii) of a mixture consisting of or comprising: at least one such compound of formula 2 as well as at least one compound of formula 1 and/or at least one compound of formula 3, wherein R1, R2, R3, R4, R5 and R6 independently of one another represent a C2-C4-alkyl or -alkenyl radical, as a fragrance or flavouring is described.
DIMERES ET OLIGOMERES DES DITHIOACIDES ALIPHATIQUES OBTENUS PAR ACTION DE PEROXYDES OU DU RAYONNEMENT U. V.
Bonnans-Plaisance, Chantal,Mahjoub, Ahmed,Levesque, Guy
, p. 1941 - 1942 (2007/10/02)
Carbodithioic acids when heated with peroxydes lead to linear oligomers whose thermolysis gives rise to trithiolannes and tetrathiannes; U V irradiation leads to tetrathianne and cyclic oligomers.
