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CS-W001157 4
Total: USD 88.00

(R)-4-Methyl-1,3,2-dioxathiolane 2,2-dioxide

  • CAS No. 1006381-03-8

  • Cat. No. CS-0084570
  • Purity≥98%
  • MDL No.MFCD26131319

*For research and further manufacturing use only, not for direct human use.

(R)-4-Methyl-1,3,2-dioxathiolane 2,2-dioxide|CS-0084570

Structure of 1006381-03-8

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General Information

  • CAS No. 1006381-03-8
  • Cat. No. CS-0084570
  • Purity ≥98%
  • MDL No. MFCD26131319
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₃H₆O₄S
  • Molecular Weight None
  • Synonym(s) 1,3,2-Dioxathiolane, 4-methyl-, 2,2-dioxide, (4R)-
  • SMILES O=S1(OC[C@@H](C)O1)=O

Description

(R)-4-Methyl-1,3,2-dioxathiolane 2,2-dioxide is a chiral sulfone-containing heterocycle featuring a stereogenic center at the C4 position. This bench-stable, moisture-tolerant scaffold integrates readily into asymmetric synthesis workflows, serving as a key building block for sulfur-based pharmaceutical intermediates and functionalized organic molecules.

Application

(R)-4-Methyl-1,3,2-dioxathiolane 2,2-dioxide serves as a stable, bench-ready chiral synthon for the construction of sulfonate-containing heterocycles. Its well-defined stereochemistry enables stereoselective transformations in asymmetric synthesis, particularly in the development of nucleoside analogs and sulfonamide-based pharmaceutical intermediates. The molecule exhibits excellent functional group tolerance and facilitates efficient coupling reactions under mild conditions, making it a practical choice for complex molecule assembly in medicinal chemistry workflows.

Safety Information

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GHS Pictogram :
GHS No : GHS06
Signal Word : Danger
UN#: 2810
Class : 6.1
Packing Group : Ⅲ
Hazard Statements : H302-H340
Precautionary Statements : P264-P270-P330-P405-P501

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Computational Chemistry Data

  • TPSA   52.6
  • LogP   -0.3335
  • H_Acceptors   4
  • H_Donors   0
  • Rotatable_Bonds   0

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