Date published: 2026-4-5

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Ethyl bromopyruvate (CAS 70-23-5)

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Application:
Ethyl bromopyruvate is a compound used in the synthesis of thioxothiazolidines from carbon disulfide and primary amines
CAS Number:
70-23-5
Molecular Weight:
195.01
Molecular Formula:
C5H7BrO3
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 bromopyruvate is a brominated derivative of pyruvic acid, featuring an ethyl group esterified to the carboxylic acid, which plays a significant role in synthetic chemistry and biochemical research. This compound serves as a pivotal reagent in the synthesis of a wide array of chemical entities, due to its reactivity particularly in nucleophilic substitution reactions that leverage its halogen atom for the introduction of various functional groups. In research applications, ethyl bromopyruvate is often utilized to study metabolic pathways, where its role in inhibiting certain enzymes involved in glycolysis and the Krebs cycle is of particular interest. This inhibition is valuable in elucidating the mechanisms through which cells manage energy production and regulation, thereby offering insights into the metabolic processes fundamental to cellular function. Its utility extends to the synthesis of heterocyclic compounds, where it acts as a precursor in reactions forming the backbone of many biologically relevant molecules, demonstrating its versatility and importance in both organic synthesis and biochemical investigation.


Ethyl bromopyruvate (CAS 70-23-5) References

  1. Synthesis of functionalized 5-imino-2,5-dihydro-furans through the reaction of isocyanides with activated acetylenes in the presence of ethyl bromopyruvate.  |  Yavari, I., et al. 2006. Mol Divers. 10: 479-82. PMID: 16967197
  2. Variable involvement of the perivascular retinal tissue in carbonic anhydrase inhibitor induced relaxation of porcine retinal arterioles in vitro.  |  Kehler, AK., et al. 2007. Invest Ophthalmol Vis Sci. 48: 4688-93. PMID: 17898293
  3. A one-pot catalyst-free synthesis of functionalized pyrrolo[1,2-a]quinoxaline derivatives from benzene-1,2-diamine, acetylenedicarboxylates and ethyl bromopyruvate.  |  Piltan, M., et al. 2013. Beilstein J Org Chem. 9: 510-5. PMID: 23616791
  4. The Mycobacterium tuberculosis H37Ra gene MRA_1916 causes growth defects upon down-regulation.  |  Singh, KS. and Singh, SK. 2015. Sci Rep. 5: 16131. PMID: 26531045
  5. Sulfuryl transfer catalyzed by pyruvate kinase.  |  Peliska, JA. and O'Leary, MH. 1989. Biochemistry. 28: 1604-11. PMID: 2719922
  6. Repurposing ethyl bromopyruvate as a broad-spectrum antibacterial.  |  Kumar, A., et al. 2019. J Antimicrob Chemother. 74: 912-920. PMID: 30689890
  7. Synthesis, antioxidant, antimicrobial and antiviral docking studies of ethyl 2-(2-(arylidene)hydrazinyl)thiazole-4-carboxylates.  |  Haroon, M., et al. 2021. Z Naturforsch C J Biosci. 76: 467-480. PMID: 33901389
  8. Synthesis, crystal structure, Hirshfeld surface investigation and comparative DFT studies of ethyl 2-[2-(2-nitrobenzylidene)hydrazinyl]thiazole-4-carboxylate.  |  Haroon, M., et al. 2022. BMC Chem. 16: 18. PMID: 35317817
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  10. Design, synthesis and evaluation of 2, 6, 8-substituted Imidazopyridine derivatives as potent PI3Kα inhibitors.  |  Chen, R., et al. 2023. J Enzyme Inhib Med Chem. 38: 2155638. PMID: 36650905
  11. Research on heterocyclic compounds. XVIII. Imidazo[2,1-b]-1,3,4-thiadiazole derivatives.  |  Abignente, E., et al. 1985. Farmaco Sci. 40: 190-9. PMID: 3874092
  12. Synthesis and antitumor activity of 2-beta-D-ribofuranosylselenazole-4- carboxamide and related derivatives.  |  Srivastava, PC. and Robins, RK. 1983. J Med Chem. 26: 445-8. PMID: 6827564
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Ethyl bromopyruvate, 5 g

sc-252799
5 g
$22.00

Ethyl bromopyruvate, 25 g

sc-252799A
25 g
$66.00