Oxidation of thiocarbamidates. 10. α-Carbamoyl sulfoxides and sulfones. 2. Formation of thiosulfonates by hydrolysis of cyclic α-carbamoyl sulfoxides was written by Hanefeld, Wolfgang;Jalili, Mohamed A.. And the article was included in Liebigs Annalen der Chemie in 1986.SDS of cas: 16312-21-3 This article mentions the following:
RNHCOCH2CH2SO2SCH2CH2CONHR (R = Me, Ph, PhCH2, PhCH2CH2) and RNHCOCH2SO2SCH2CONHR (R = Ph, PhCH2, p-ClC6H4CH2) were prepared by hydrolysis of the thiazine oxides I and thiazolidine oxide II. Structures were confirmed by independent synthesis. In the experiment, the researchers used many compounds, for example, 3-Methylthiazolidine-2,4-dione (cas: 16312-21-3SDS of cas: 16312-21-3).
3-Methylthiazolidine-2,4-dione (cas: 16312-21-3) belongs to thiazolidine derivatives. Thiazolidines undergo hydrolysis to aldehyde and amino thiol under acid or basic aqueous conditions. Thiazolidine and its composites are key components of many natural products and drugs , and are also present in many synthetic compounds such as anticancer, anti-inflammatory, antitubercular, antifungal, antiviral, anti-HIV, cytotoxicity, antitrypanosomal, antinociceptive and anti-hypernociceptive compounds.SDS of cas: 16312-21-3
Referemce:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com