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Structure of 1185100-09-7
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This piperidine derivative features a propargyloxy-functionalized heterocycle, enabling efficient conjugation via copper-catalyzed azide-alkyne cycloaddition. The hydrochloride salt enhances solubility and stability under standard handling conditions, facilitating integration into bioconjugation workflows and medicinal chemistry campaigns requiring robust, modular linkers.
4-(Prop-2-yn-1-yloxy)piperidine hydrochloride serves as a versatile building block for copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions, enabling efficient access to triazole-linked scaffolds. The propargylic ether functionality exhibits excellent bench stability and compatibility with diverse functional groups, facilitating straightforward purification and integration into medicinal chemistry campaigns. Its hydrochloride salt form enhances solubility and handling in aqueous and polar organic media.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P501
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Lot numbers can be found on the outside label of a product: