Atomfair 1,5,2,4-Dioxadithiane 2,2,4,4-tetraoxide C2H4O6S2

Description 1,5,2,4-Dioxadithiane 2,2,4,4-tetraoxide (CAS No. 99591-74-9) is a high-purity sulfone-based organic compound with the molecular formula C2H4O6S2. This specialized chemical features a unique cyclic structure containing two sulfur atoms and two oxygen atoms in a dioxadithiane framework, each sulfur center oxidized to a sulfone group (SO2). With a molecular weight of 188.18 g/mol, this compound is offered as a white crystalline powder with ??95% purity (HPLC), ideal for advanced research applications. Its distinctive tetraoxidized structure makes it valuable for studying sulfone reactivity, heterocyclic chemistry, and as a potential building block for specialty polymers or energetic materials. Proper storage at 2-8??C…

Description

1,5,2,4-Dioxadithiane 2,2,4,4-tetraoxide (CAS No. 99591-74-9) is a high-purity sulfone-based organic compound with the molecular formula C₂H₄O₆S₂. This specialized chemical features a unique cyclic structure containing two sulfur atoms and two oxygen atoms in a dioxadithiane framework, each sulfur center oxidized to a sulfone group (SO₂). With a molecular weight of 188.18 g/mol, this compound is offered as a white crystalline powder with ??95% purity (HPLC), ideal for advanced research applications. Its distinctive tetraoxidized structure makes it valuable for studying sulfone reactivity, heterocyclic chemistry, and as a potential building block for specialty polymers or energetic materials. Proper storage at 2-8??C in a tightly sealed container is recommended to maintain stability.

CAS No: 99591-74-9
Molecular Formula: C2H4O6S2
Molecular Weight: 188.18
Exact Mass: 187.94493019
Monoisotopic Mass: 187.94493019
IUPAC Name: 1,5,2,4-dioxadithiane 2,2,4,4-tetraoxide
SMILES: C1OS(=O)(=O)CS(=O)(=O)O1
Synonyms: 1,5,2,4-dioxadithiane 2,2,4,4-tetraoxide, 1,5,2,4-Dioxadithiane, 2,2,4,4-tetraoxide, DTXSID60469235, EC 700-464-0, DTXCID70420054

Application

This tetraoxidized dioxadithiane derivative serves as a key intermediate in the synthesis of specialty sulfur-containing heterocycles. Researchers utilize it as a model compound for studying sulfone reactivity patterns in organic transformations. The compound shows potential as a precursor for high-performance polymer electrolytes due to its multiple polar sulfone groups. In materials science, it may be employed as a crosslinking agent or oxidant in controlled reactions.

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