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Structure of 182223-54-7
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4-Benzyloxycarbonylamino-piperidine features a protected piperidine core with a benzyloxycarbonyl group at the nitrogen, enabling stable incorporation into peptide synthesis. The benzyl ester moiety facilitates selective deprotection under mild hydrogenolysis conditions, preserving sensitive functional groups elsewhere in the molecule. This derivative serves as a key intermediate for bioactive amine-containing compounds in medicinal chemistry and combinatorial libraries.
4-Benzyloxycarbonylamino-piperidine serves as a versatile scaffold for the synthesis of bioactive heterocycles and peptide analogs. The benzyloxycarbonyl (Z) group provides orthogonal protection for amine functionalities, enabling selective transformations during multistep syntheses. Its stability under standard reaction conditions and ease of removal via catalytic hydrogenation facilitate efficient downstream processing. This compound functions effectively in solid-phase and solution-phase peptide coupling protocols, offering reliable access to piperidine-based pharmacophores.
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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: