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Structure of 160809-38-1
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1-Benzyl 4-ethyl piperidine-1,4-dicarboxylate features a rigid piperidine core with orthogonal ester handles, enabling selective functionalization in medicinal chemistry. The benzyl group enhances solubility and stability, while the ethyl substituent provides optimal steric profile for downstream derivatization. This scaffold integrates readily into complex heterocyclic architectures under standard conditions.
1-Benzyl 4-ethyl piperidine-1,4-dicarboxylate serves as a versatile diester building block in synthetic organic chemistry, enabling the construction of substituted piperidine scaffolds prevalent in medicinal chemistry. Its bench-stable nature and orthogonal functional group tolerance facilitate downstream transformations, including selective reduction, hydrolysis, and cyclization reactions. The molecule functions effectively in multi-step syntheses for heterocyclic intermediates and API precursors.
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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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: