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Structure of 1219827-56-1
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tert-Butyl 4-(prop-2-yn-1-yloxy)piperidine-1-carboxylate features a propargyl ether linkage that enables efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC), facilitating rapid conjugation in bioorthogonal labeling. The piperidine core offers favorable solubility and stability under standard bench conditions, while the tert-butyl carbamate group provides robust protection for amine functionalities during synthetic manipulations.
tert-Butyl 4-(prop-2-yn-1-yloxy)piperidine-1-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to piperidine-based scaffolds via orthogonal deprotection and click chemistry. The propargyloxy group facilitates CuAAC reactions, while the tert-butoxycarbonyl (Boc) group provides stable protection under standard conditions. Its bench-stable nature and compatibility with diverse functional groups make it ideal for modular synthesis of bioactive molecules.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
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Lot numbers can be found on the outside label of a product: