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Structure of 138163-07-2
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1-Benzyl 4-methyl piperidine-1,4-dicarboxylate features a rigid piperidine core with strategically positioned benzyl and methyl substituents, enabling precise stereochemical control in asymmetric synthesis. The dicarboxylate functionality offers dual handles for derivatization, while the benzylic protection enhances stability under standard reaction conditions. This scaffold serves as a key intermediate in medicinal chemistry campaigns targeting CNS-active compounds.
1-Benzyl 4-methyl piperidine-1,4-dicarboxylate serves as a versatile chiral building block in medicinal chemistry, enabling efficient access to piperidine-based pharmacophores. Its dual ester functionality supports selective deprotection and functionalization, while the benzyl group offers orthogonal protection and enhanced stability. The molecule facilitates C–H activation, reductive amination, and transition-metal-catalyzed coupling reactions, making it valuable for constructing complex heterocyclic scaffolds under standard laboratory conditions.
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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: