CAS 35371-97-2
:1,2,4-Dithiazolidine-3,5-dione
Description:
1,2,4-Dithiazolidine-3,5-dione, identified by its CAS number 35371-97-2, is a heterocyclic compound featuring a five-membered ring containing two sulfur atoms and two nitrogen atoms, along with two carbonyl groups. This compound is characterized by its unique structural arrangement, which contributes to its reactivity and potential applications in organic synthesis. It typically appears as a solid at room temperature and is soluble in polar solvents. The presence of the dione functional groups makes it a potential candidate for various chemical reactions, including nucleophilic additions and cycloadditions. Additionally, 1,2,4-dithiazolidine-3,5-dione may exhibit biological activity, making it of interest in medicinal chemistry. Its stability and reactivity can be influenced by environmental factors such as pH and temperature. Overall, this compound serves as a valuable building block in the synthesis of more complex molecules and may have implications in various fields, including pharmaceuticals and materials science.
Formula:C2HNO2S2
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Found 1 products.
1,2,4-Dithiazolidine-3,5-dione
CAS:<p>1,2,4-Dithiazolidine-3,5-dione is a disulfide bond compound that contains a nucleophilic cysteine residue. It is oxidized to the corresponding sulfoxide or sulfone by reaction with hydrochloric acid. 1,2,4-Dithiazolidine-3,5-dione has been shown to react with amines to form adducts. The nucleophilic attack of the sulfur atom on the carbonyl carbon generates an intermediate thioketal and leaves the original disulfide intact. The nucleophilic attack leads to a number of possible products including dithioesters and dithioimidates. Both these products are stable in water and can be used in organic synthesis reactions such as DNA duplex formation.</p>Formula:C2HNO2S2Purity:Min. 95%Color and Shape:PowderMolecular weight:135.16 g/mol
