Date published: 2025-12-29

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Methyl (4R,5S)-2,2,5-trimethyl-1,3-dioxolane-4-carboxylate (CAS 78086-72-3)

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CAS Number:
78086-72-3
Purity:
≥90%
Molecular Weight:
174.19
Molecular Formula:
C8H14O4
Supplemental Information:
This is as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Methyl (4R,5S)-2,2,5-trimethyl-1,3-dioxolane-4-carboxylate is a key intermediate in organic synthesis, notably in the construction of complex molecules with pharmaceutical and agrochemical relevance. Its mechanism of action primarily involves its role as a versatile building block in the synthesis of chiral molecules. Chemists utilize its unique structural features to introduce chirality into target molecules, enabling the creation of enantiomerically pure compounds with desired stereochemical configurations. This chemical has found extensive use in asymmetric synthesis strategies, such as chiral pool synthesis, enzymatic resolution, and asymmetric catalysis, where its stereochemical integrity is crucial for controlling the stereochemistry of the final product. Moreover, researchers have employed methyl (4R,5S)-2,2,5-trimethyl-1,3-dioxolane-4-carboxylate in the total synthesis of natural products, pharmaceutical intermediates, and biologically active compounds. By incorporating this compound into synthetic routes, scientists have been able to access diverse chemical space and explore structure-activity relationships, aiding in the development of new drug candidates, agrochemicals, and functional materials. Additionally, its use in the synthesis of chiral ligands and catalysts has contributed to advances in asymmetric catalysis, enabling efficient and selective transformations in organic chemistry research.


Methyl (4R,5S)-2,2,5-trimethyl-1,3-dioxolane-4-carboxylate (CAS 78086-72-3) References

  1. Synthesis and evaluation of optically pure dioxolanes as inhibitors of hepatitis C virus RNA replication.  |  Bera, S., et al. 2003. Bioorg Med Chem Lett. 13: 4455-8. PMID: 14643345
  2. Synthesis and biological evaluation of 5R- and 5S-methyl substituted D- and L-configuration 1,3-dioxolane nucleoside analogs.  |  Bera, S., et al. 2004. Bioorg Med Chem. 12: 6237-47. PMID: 15519166

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Methyl (4R,5S)-2,2,5-trimethyl-1,3-dioxolane-4-carboxylate, 5 ml

sc-253012
5 ml
$162.00