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Structure of 86945-25-7
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This amine integrates a benzylpiperidine pharmacophore with an ethylamine tether, enabling facile conjugation in medicinal chemistry. The piperidine nitrogen and terminal amine offer dual functionalization sites, while the benzyl group enhances lipophilicity and target engagement. Designed for rapid derivatization in drug discovery workflows.
2-(1-Benzylpiperidin-4-yl)ethan-1-amine serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles through standard amine functionalization and coupling reactions. Its piperidine core offers favorable solubility and metabolic stability, while the pendant benzyl and ethylamine groups provide orthogonal reactivity for conjugation or cyclization. The compound exhibits good bench stability and is readily purified by standard chromatographic methods, facilitating integration into multi-step syntheses of CNS-targeted pharmaceuticals and kinase inhibitors.
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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: