Date published: 2025-9-5

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Ethyl 2-oxo-4-phenylbutyrate (CAS 64920-29-2)

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CAS Number:
64920-29-2
Molecular Weight:
206.24
Molecular Formula:
C12H14O3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Ethyl 2-oxo-4-phenylbutyrate functions as a chemical intermediate in a range of chemical applications. It acts as a precursor in the synthesis of various organic compounds, contributing to the formation of complex molecular structures. At the molecular level, Ethyl 2-oxo-4-phenylbutyrate participates in reactions that lead to the production of diverse derivatives with potential applications in experimental applications. Its mechanism of action involves undergoing specific chemical transformations, enabling the generation of novel compounds with distinct properties. Ethyl 2-Oxo-4-Phenylbutyrate′s functional role lies in its ability to serve as a building block for the creation of new molecules, thereby contributing to the expansion of chemical libraries and the exploration of diverse chemical space.


Ethyl 2-oxo-4-phenylbutyrate (CAS 64920-29-2) References

  1. Effect of ionic liquid [BMIM][PF6] on asymmetric reduction of ethyl 2-oxo-4-phenylbutyrate by Saccharomyces cerevisiae.  |  Shi, YG., et al. 2008. J Ind Microbiol Biotechnol. 35: 1419-24. PMID: 18716813
  2. Efficient synthesis of a chiral precursor for angiotensin-converting enzyme (ACE) inhibitors in high space-time yield by a new reductase without external cofactors.  |  Shen, ND., et al. 2012. Org Lett. 14: 1982-5. PMID: 22480179
  3. Assessing the stereoselectivity of carbonyl reductases toward the reduction of OPBE and docking analysis.  |  Chen, R., et al. 2016. Biotechnol Appl Biochem. 63: 465-70. PMID: 25989134
  4. Cloning and characterization of three ketoreductases from soil metagenome for preparing optically active alcohols.  |  Zhao, Z., et al. 2016. Biotechnol Lett. 38: 1799-808. PMID: 27383399
  5. Evolution of Glucose Dehydrogenase for Cofactor Regeneration in Bioredox Processes with Denaturing Agents.  |  Qian, WZ., et al. 2020. Chembiochem. 21: 2680-2688. PMID: 32324965
  6. Coupling of Bioreaction and Separation via Novel Thermosensitive Ionic Liquids Applied in the Baker's Yeast-Catalyzed Reduction of Ethyl 2-oxo-4-phenylbutyrate.  |  Yang, Y., et al. 2020. Molecules. 25: PMID: 32354057
  7. Reversal of Regioselectivity in Zinc-Dependent Medium-Chain Alcohol Dehydrogenase from Rhodococcus erythropolis toward Octanone Derivatives.  |  Dhoke, GV., et al. 2020. Chembiochem. 21: 2957-2965. PMID: 32415803
  8. Construction of Bi-Enzyme Self-Assembly Clusters Based on SpyCatcher/SpyTag for the Efficient Biosynthesis of (R)-Ethyl 2-hydroxy-4-phenylbutyrate.  |  Wang, J., et al. 2023. Biomolecules. 13: PMID: 36671476

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Ethyl 2-oxo-4-phenylbutyrate, 5 g

sc-239895
5 g
$56.00