Ceriometric studies of thiazolidinedione and some of its 3-substituted derivatives was written by Turkevich, N. M.;Dmitrishin, R. T.. And the article was included in Vestnik L’vovskogo Politekhnicheskogo Instituta in 1975.Name: 3-Methylthiazolidine-2,4-dione This article mentions the following:
Thiazolidinedione (I; R = H) was oxidized by aqueous Ce4+ to give S2(CH2CO2H)2 (II), NH4+, and CO2; I (R = Me) gave II, MeNH3+, and CO2 under the same conditions. Analogous treatment of I (R = C6H4OEt-p) afforded I (R = C6H4OH-p) and AcOH, an excess Ce4+ converted I (R = C6H4OH-p, Ph) to II, benzoquinone, CO2, and N. In the experiment, the researchers used many compounds, for example, 3-Methylthiazolidine-2,4-dione (cas: 16312-21-3Name: 3-Methylthiazolidine-2,4-dione).
3-Methylthiazolidine-2,4-dione (cas: 16312-21-3) belongs to thiazolidine derivatives. Thiazolidine motifs are very intriguing heterocyclic five-membered moieties present in diverse natural and bioactive compounds having sulfur at the first position and nitrogen at the third position. Thiazolidines have been applied as prodrug derivatives for various steroids containing a 3-carbonyl group to improve their topical anti-inflammatory activity. Name: 3-Methylthiazolidine-2,4-dione
Referemce:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com