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Atomfair 4-Methyl-1,2-oxathiolane 2,2-dioxide C4H8O3S
Description 4-Methyl-1,2-oxathiolane 2,2-dioxide (CAS No. 15606-89-0) is a high-purity sulfone derivative with the molecular formula C4H8O3S . This specialized cyclic sulfone compound is widely utilized in organic synthesis, pharmaceutical research, and material science due to its unique structural and reactive properties. Its IUPAC name, 4-methyloxathiolane 2,2-dioxide , reflects its oxathiolane core with a methyl substituent at the 4-position and two sulfonyl oxygen atoms. Available in various quantities, this product is rigorously tested for purity (typically ??95% by GC or HPLC) and stability, ensuring optimal performance in demanding applications. Suitable for researchers and industrial scientists, it is supplied with comprehensive analytical…
Description
Description
4-Methyl-1,2-oxathiolane 2,2-dioxide (CAS No. 15606-89-0) is a high-purity sulfone derivative with the molecular formula C4H8O3S. This specialized cyclic sulfone compound is widely utilized in organic synthesis, pharmaceutical research, and material science due to its unique structural and reactive properties. Its IUPAC name, 4-methyloxathiolane 2,2-dioxide, reflects its oxathiolane core with a methyl substituent at the 4-position and two sulfonyl oxygen atoms. Available in various quantities, this product is rigorously tested for purity (typically ??95% by GC or HPLC) and stability, ensuring optimal performance in demanding applications. Suitable for researchers and industrial scientists, it is supplied with comprehensive analytical data (NMR, MS, FTIR) and handled under strict quality control protocols.
- CAS No: 15606-89-0
- Molecular Formula: C4H8O3S
- Molecular Weight: 136.17
- Exact Mass: 136.01941529
- Monoisotopic Mass: 136.01941529
- IUPAC Name: 4-methyloxathiolane 2,2-dioxide
- SMILES: CC1COS(=O)(=O)C1
- Synonyms: 15606-89-0, 4-methyl-1,2-oxathiolane 2,2-dioxide, 1,2-Oxathiolane, 4-methyl-, 2,2-dioxide, 4-methyloxathiolane 2,2-dioxide, NSC48096
Application
4-Methyl-1,2-oxathiolane 2,2-dioxide serves as a versatile intermediate in the synthesis of sulfone-containing pharmaceuticals and agrochemicals. Its reactive sulfone group enables participation in C?CS bond-forming reactions, making it valuable for constructing heterocyclic scaffolds. Researchers also employ it as a polar aprotic solvent additive or electrolyte component in specialty battery formulations. Additionally, it finds niche use in polymer chemistry as a monomer or crosslinking agent for sulfone-based materials.
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