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Structure of 90892-99-2
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Ethyl 4-methyloxazole-2-carboxylate features a sterically hindered oxazole ring with a pendant ethyl ester and methyl group, enabling direct functionalization at the C4 position. This configuration enhances stability under standard reaction conditions while facilitating efficient coupling in heterocyclic synthesis.
Ethyl 4-methyloxazole-2-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to oxazole-containing scaffolds via standard functional group transformations. Its stability under common reaction conditions and compatibility with palladium-catalyzed couplings facilitate downstream derivatization. The ester functionality allows for selective hydrolysis or reduction, while the electron-deficient oxazole ring supports nucleophilic substitution at C5. This compound functions effectively in medicinal chemistry campaigns requiring robust, synthetically accessible heterocycles.
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Lot numbers can be found on the outside label of a product: