Atomfair 1,2,6-Oxadithiane, 2,2,6,6-tetraoxide C3H6O5S2

Description 1,2,6-Oxadithiane 2,2,6,6-tetraoxide (CAS No. 4720-58-5) is a high-purity sulfone derivative with the molecular formula C3H6O5S2. This specialized heterocyclic compound features a unique oxadithiane core structure with two sulfonyl functional groups, making it a valuable intermediate for advanced organic synthesis and pharmaceutical research. Our product is rigorously tested to ensure >98% purity by HPLC, with full characterization data including1H NMR,13C NMR, and mass spectrometry available upon request. Supplied as a white crystalline powder with excellent stability under recommended storage conditions (2-8??C in inert atmosphere). Ideal for researchers developing novel sulfone-containing compounds, asymmetric catalysts, or studying structure-activity relationships in medicinal chemistry…

Description

Description

1,2,6-Oxadithiane 2,2,6,6-tetraoxide (CAS No. 4720-58-5) is a high-purity sulfone derivative with the molecular formula C3H6O5S2. This specialized heterocyclic compound features a unique oxadithiane core structure with two sulfonyl functional groups, making it a valuable intermediate for advanced organic synthesis and pharmaceutical research. Our product is rigorously tested to ensure >98% purity by HPLC, with full characterization data including 1H NMR, 13C NMR, and mass spectrometry available upon request. Supplied as a white crystalline powder with excellent stability under recommended storage conditions (2-8??C in inert atmosphere). Ideal for researchers developing novel sulfone-containing compounds, asymmetric catalysts, or studying structure-activity relationships in medicinal chemistry applications.

  • CAS No: 4720-58-5
  • Molecular Formula: C3H6O5S2
  • Molecular Weight: 186.2
  • Exact Mass: 185.96566563
  • Monoisotopic Mass: 185.96566563
  • IUPAC Name: 1,2,6-oxadithiane 2,2,6,6-tetraoxide
  • SMILES: C1CS(=O)(=O)OS(=O)(=O)C1
  • Synonyms: 4720-58-5, 1,2,6-Oxadithiane, 2,2,6,6-tetraoxide, SCHEMBL139980, DTXSID90480493, AVPYLKIIPLFMHQ-UHFFFAOYSA-N

Application

This sulfone derivative serves as a versatile building block in organic synthesis, particularly for constructing complex heterocyclic systems. Researchers utilize it in the development of novel pharmaceutical intermediates with potential biological activity. The compound’s unique structure makes it valuable for studying sulfone reactivity patterns in nucleophilic substitution reactions. It has shown utility in materials science for creating specialized polymers with enhanced thermal stability.

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