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Structure of 259180-77-3
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1-Boc-3-(2-aminoethyl)piperidine features a protected primary amine and a piperidine ring, enabling direct incorporation into peptide and small-molecule conjugates. The Boc group ensures stability during synthetic manipulations and facilitates selective deprotection under mild acidic conditions. This scaffold serves as a key building block in bioconjugation and medicinal chemistry applications.
1-Boc-3-(2-aminoethyl)piperidine serves as a versatile building block in medicinal chemistry, enabling efficient access to piperidine-based scaffolds through straightforward deprotection and functionalization. The Boc group provides excellent bench stability and facilitates purification, while the primary amine supports diverse coupling reactions and cyclization strategies. This compound functions reliably in standard peptide and small-molecule synthesis workflows.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 2735
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302+H312+H332-H314
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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: