Description
4,6-Dimethyl-[1,3,2]dioxathiane 2,2-dioxide (CAS No. 63082-73-5) is a high-purity organic sulfone compound with the molecular formula C5H10O4S. This heterocyclic compound features a six-membered dioxathiane ring with two methyl substituents at the 4- and 6-positions and a sulfone functional group. Its IUPAC name is 4,6-dimethyl-1,3,2-dioxathiane 2,2-dioxide, and it is characterized by its stability, low volatility, and solubility in common organic solvents. This reagent is rigorously tested for quality and is ideal for use in organic synthesis, pharmaceutical research, and material science applications. Available in various packaging options to suit laboratory-scale and industrial needs.
Properties
- CAS Number: 63082-73-5
- Complexity: 186
- IUPAC Name: 4,6-dimethyl-1,3,2-dioxathiane 2,2-dioxide
- InChI: InChI=1S/C5H10O4S/c1-4-3-5(2)9-10(6,7)8-4/h4-5H,3H2,1-2H3
- InChI Key: SNUUNBNYJHRNPG-UHFFFAOYSA-N
- Exact Mass: 166.02997997
- Molecular Formula: C5H10O4S
- Molecular Weight: 166.20
- SMILES: CC1CC(OS(=O)(=O)O1)C
- Topological: 61
- Monoisotopic Mass: 166.02997997
- Synonyms: 63082-73-5, 4,6-dimethyl-1,3,2lambda6-dioxathiane-2,2-dione, 4,6-dimethyl-[1,3,2]dioxathiane 2,2-dioxide, 4,6-dimethyl-1,3,2-dioxathiane 2,2-dioxide, SCHEMBL8468962, EN300-1609288
Application
4,6-Dimethyl-[1,3,2]dioxathiane 2,2-dioxide is primarily used as a versatile intermediate in organic synthesis, particularly in the preparation of sulfone-containing compounds. It serves as a key building block for pharmaceuticals, agrochemicals, and specialty materials due to its stable sulfone moiety. Researchers also employ it in the development of novel heterocyclic frameworks and as a precursor in catalytic reactions. Its unique structure makes it valuable in studying reaction mechanisms involving sulfones.
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