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Structure of 163210-40-0
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tert-Butyl 4-(2-hydroxyethoxy)piperidine-1-carboxylate features a piperidine core functionalized with a hydroxyethoxy side chain and a tert-butyl carbamate protecting group. This bifunctional scaffold enables direct incorporation into complex molecular architectures, offering orthogonal reactivity for late-stage derivatization in medicinal chemistry campaigns. The pendant hydroxyl group supports further modification via esterification or glycosylation, while the stable tert-butoxycarbonyl moiety facilitates purification and handling under standard bench conditions.
tert-Butyl 4-(2-hydroxyethoxy)piperidine-1-carboxylate serves as a versatile piperidine-based building block, enabling efficient access to bioactive heterocycles through orthogonal functionalization. The pendant hydroxyethyl group facilitates downstream derivatization via etherification or esterification, while the tert-butyl carbamate provides robust protection under standard reaction conditions. Its bench-stable nature and compatibility with diverse coupling protocols make it well-suited for medicinal chemistry campaigns requiring flexible piperidine scaffolds.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: