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Structure of 5166-67-6
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Ethyl N-methylpiperidine-3-carboxylate features a sterically hindered piperidine core with a strategically positioned ester group, enabling direct functionalization at the 3-position. This bench-stable intermediate facilitates efficient coupling reactions in medicinal chemistry workflows, particularly for constructing complex heterocyclic scaffolds.
Ethyl N-methylpiperidine-3-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to piperidine-based scaffolds. Its ester functionality facilitates selective transformations, while the N-methyl group enhances metabolic stability and modulates basicity. The compound exhibits good bench stability, ease of purification, and compatibility with standard coupling and reduction protocols, making it well-suited for iterative synthesis campaigns targeting bioactive molecules.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352
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Lot numbers can be found on the outside label of a product: