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Ethyl 2-bromooxazole-5-carboxylate

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Ethyl 2-bromooxazole-5-carboxylate Basic information

Product Name:
Ethyl 2-bromooxazole-5-carboxylate
Synonyms:
  • 5-Oxazolecarboxylic acid, 2-bromo-, ethyl ester
  • Ethyl 2-broMo-oxazol-5-carboxylate
  • 2-BroMo-oxazole-5-carboxylic acid ethyl ester
  • 2-Bromo-5-oxazolecarboxylic acid ethyl ester
  • 2-bromooxazoL
  • 2-bromooxazole-5-carboxylate
  • Ethyl 2-broMooxazole-5-carboxylate
  • ethyl 2-broMo-1,3-oxazole-5-carboxylate
CAS:
1060816-22-9
MF:
C6H6BrNO3
MW:
220.02
Mol File:
1060816-22-9.mol
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Ethyl 2-bromooxazole-5-carboxylate Chemical Properties

Boiling point:
272.2±32.0 °C(Predicted)
Density 
1.617±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
pka
-2+-.0.10(Predicted)
Appearance
Off-white to yellow Solid
InChI
InChI=1S/C6H6BrNO3/c1-2-10-5(9)4-3-8-6(7)11-4/h3H,2H2,1H3
InChIKey
VZYKDUOPMKESLS-UHFFFAOYSA-N
SMILES
O1C(C(OCC)=O)=CN=C1Br
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Safety Information

HS Code 
2934999090
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Ethyl 2-bromooxazole-5-carboxylate Usage And Synthesis

Uses

Ethyl 2-bromooxazole-5-carboxylate is an organic synthesis intermediate. In the synthesis of novel topoisomerase II inhibitors (such as IID432), this compound serves as a coupling substrate for the construction of the oxazole ring core structure [1].

References

[1] Olivier René, Manuel Saldivia, Maxime Dauphinais, et al. (2026). Discovery of IID432 for Chagas Disease: A Cyanotriazole Inhibitor of Trypanosoma cruzi Topoisomerase II Achieves Sterile Cure After Short-Term Treatment in a Chronic Infection Model. Journal of medicinal chemistry, 69(2), 1135–1153. https://doi.org/10.1021/acs.jmedchem.5c02459

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