ChemicalBook > Product Catalog > Pharmaceutical intermediates > Heterocyclic compound > Ethyl 2-bromooxazole-5-carboxylate
Ethyl 2-bromooxazole-5-carboxylate
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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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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