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Structure of 39143-25-4
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4-Amino-1-benzylpiperidine-4-carboxylic acid features a rigid piperidine core functionalized with a benzyl group at N1 and a carboxylic acid at C4, enabling integration into bioactive scaffolds. The para-amino substitution enhances hydrogen bonding capacity, while the benzylic linkage provides structural rigidity and favorable lipophilicity for membrane permeability in CNS-targeted compounds.
4-Amino-1-benzylpiperidine-4-carboxylic acid serves as a versatile building block for medicinal chemistry, enabling the synthesis of piperidine-based scaffolds prevalent in CNS-targeted therapeutics. Its amine and carboxylic acid functionalities offer orthogonal reactivity for peptide coupling, amidation, and derivatization. The benzyl group enhances metabolic stability and modulates lipophilicity, while the 4-amino substituent facilitates further functionalization. Bench-stable and readily purified via standard chromatographic methods, it supports scalable synthesis and integration into complex molecular architectures.
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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: