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Structure of 156185-63-6
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tert-Butyl 4-(3-hydroxypropyl)tetrahydropyridine-1(2H)-carboxylate features a bench-stable tetrahydropyridine core bearing a pendant hydroxyl-functionalized alkyl chain. This bifunctional scaffold integrates a protected amine and a reactive alcohol, enabling sequential derivatization in medicinal chemistry campaigns. The tert-butyl ester group ensures compatibility with standard deprotection protocols.
tert-Butyl 4-(3-hydroxypropyl)tetrahydropyridine-1(2H)-carboxylate serves as a versatile scaffold for the synthesis of bioactive heterocycles, enabling efficient access to functionalized tetrahydropyridine cores. The pendant hydroxyl group facilitates downstream derivatization via oxidation, esterification, or ether formation, while the tert-butyl carbamate offers protection and ease of removal under mild acidic conditions. Its bench-stable nature and compatibility with standard coupling and reduction protocols make it a practical building block in medicinal chemistry campaigns.
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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-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: