Atomfair 1,3,2-Dioxathiane, 2,2-dioxide C3H6O4S

Description 1,3,2-Dioxathiane 2,2-Dioxide (CAS No. 1073-05-8) is a high-purity cyclic sulfate compound with the molecular formula C3H6O4S . This versatile reagent is widely utilized in organic synthesis, particularly as a key intermediate for the preparation of complex molecules such as deoxy salacinols. Its cyclic sulfate structure offers excellent reactivity in coupling reactions, enabling efficient functionalization of target compounds. The product is supplied as a white to off-white crystalline solid with ??98% purity (HPLC), ensuring consistent performance in demanding research applications. Suitable for use under inert conditions, it is packaged in amber glass bottles to maintain stability and prevent degradation. Ideal…

Description

1,3,2-Dioxathiane 2,2-Dioxide (CAS No. 1073-05-8) is a high-purity cyclic sulfate compound with the molecular formula C₃H₆O₄S. This versatile reagent is widely utilized in organic synthesis, particularly as a key intermediate for the preparation of complex molecules such as deoxy salacinols. Its cyclic sulfate structure offers excellent reactivity in coupling reactions, enabling efficient functionalization of target compounds. The product is supplied as a white to off-white crystalline solid with ??98% purity (HPLC), ensuring consistent performance in demanding research applications. Suitable for use under inert conditions, it is packaged in amber glass bottles to maintain stability and prevent degradation. Ideal for pharmaceutical, agrochemical, and materials science research.

CAS No: 1073-05-8
Molecular Formula: C3H6O4S
Molecular Weight: 138.14
Exact Mass: 137.99867984
Monoisotopic Mass: 137.99867984
IUPAC Name: 1,3,2-dioxathiane 2,2-dioxide
SMILES: C1COS(=O)(=O)OC1
Synonyms: 1073-05-8, Trimethylene sulfate, 1,3,2-Dioxathiane, 2,2-dioxide, 1,3-Propylene sulfate, 1,3-Propanediol, cyclic sulfate

Application

1,3,2-Dioxathiane 2,2-Dioxide is primarily employed as a reagent in the synthesis of deoxy salacinols via coupling reactions. Its cyclic sulfate group acts as a reactive handle for nucleophilic substitution, facilitating the construction of complex glycosidic structures. Researchers also utilize it as a propylene glycol equivalent in polymer chemistry and as a precursor for sulfated organic compounds. Its stability and selectivity make it valuable for controlled functionalization in medicinal chemistry workflows.

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