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Structure of 1196145-01-3
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Benzyl 3-amino-4-oxopiperidine-1-carboxylate hydrochloride features a piperidine core with a strategically positioned amino group and ketone functionality, enabling direct incorporation into diverse heterocyclic scaffolds. The benzyl ester moiety enhances solubility and stability, while the hydrochloride salt ensures excellent crystallinity and handling ease. This compound serves as a key intermediate in the synthesis of bioactive nitrogen-containing molecules.
Benzyl 3-amino-4-oxopiperidine-1-carboxylate hydrochloride serves as a versatile building block in medicinal chemistry, enabling efficient access to piperidine-based scaffolds. Its amine and carbonyl functionalities support diverse transformations, including reductive amination, cyclization, and coupling reactions. The benzyl ester provides bench stability and facilitates straightforward deprotection, while the hydrochloride salt enhances solubility and handling—ideal for high-throughput synthesis and API development workflows.
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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: