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Structure of 183170-69-6
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tert-Butyl 4-(1-hydroxyethyl)piperidine-1-carboxylate features a chiral hydroxyethyl side chain attached to a piperidine core, enabling direct functionalization at the benzylic-like position. This bench-stable, moisture-tolerant building block integrates readily into medicinal chemistry campaigns requiring stereoselective transformations or downstream derivatization of nitrogen-containing heterocycles.
tert-Butyl 4-(1-hydroxyethyl)piperidine-1-carboxylate serves as a versatile chiral building block for medicinal chemistry, enabling direct access to piperidine-based scaffolds through mild deprotection or functionalization. The tertiary alcohol functionality offers controlled reactivity for oxidation, substitution, or coupling reactions, while the robust tert-butyl carbamate group ensures stability during multistep synthesis and facilitates purification via standard chromatographic methods.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: