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Structure of 72551-53-2
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Ethyl 1-benzylpiperidine-3-carboxylate features a benzylated piperidine core with a carboxylate ester at the C3 position, offering enhanced solubility and stability for synthetic applications. This scaffold integrates readily into complex alkaloid frameworks and serves as a key intermediate in medicinal chemistry campaigns targeting CNS modulators.
Ethyl 1-benzylpiperidine-3-carboxylate serves as a versatile scaffold for the synthesis of piperidine-based pharmaceutical intermediates. Its benzyl-protected amine and ester functionalities enable selective transformations, including hydrogenolysis, nucleophilic substitution, and coupling reactions. The compound exhibits good bench stability and facilitates efficient purification, making it well-suited for iterative medicinal chemistry campaigns and API precursor development.
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Lot numbers can be found on the outside label of a product: