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Structure of 78190-11-1
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This piperidine-based building block features a benzyl-protected carboxylic acid moiety, enabling straightforward deprotection and integration into peptide synthesis. The carbamate linkage offers stability under standard bench conditions, while the piperidine ring provides a versatile scaffold for medicinal chemistry applications.
1-[(Benzyloxy)carbonyl]-3-piperidinecarboxylic acid serves as a robust piperidine-based building block for peptide synthesis and medicinal chemistry campaigns. Its carbamate functionality enables selective N-alkylation and facilitates downstream deprotection under standard hydrogenolysis conditions. The benzyloxycarbonyl (Cbz) group provides excellent bench stability, compatibility with diverse reaction environments, and straightforward purification via crystallization or chromatography.
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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: