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Structure of 4644-61-5
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Ethyl 4-oxopiperidine-3-carboxylate hydrochloride features a stable, bench-ready piperidine core with a ketone at the C4 position and an ester-functionalized C3. This electrophilic scaffold integrates readily into synthetic sequences requiring nitrogen heterocycles with orthogonal reactivity, particularly in medicinal chemistry and peptide conjugation workflows.
Ethyl 4-oxopiperidine-3-carboxylate hydrochloride serves as a versatile building block in medicinal chemistry, enabling efficient access to piperidine-based scaffolds common in bioactive molecules. Its well-defined reactivity facilitates nucleophilic addition, reductive amination, and cyclization reactions under standard conditions. The hydrochloride salt enhances bench stability and simplifies purification, while the ester and ketone functionalities support diverse downstream transformations. This compound functions reliably in multi-step syntheses requiring functional group compatibility and predictable stereochemical outcomes.
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Lot numbers can be found on the outside label of a product: