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Structure of 149377-19-5
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tert-Butyl 4-(4-hydroxyphenyl)piperidine-1-carboxylate features a piperidine core functionalized with a para-hydroxyphenyl group and a bench-stable tert-butyl carbamate. This combination enables straightforward deprotection to yield the free amine, facilitating access to bioactive phenolic piperidines in medicinal chemistry.
tert-Butyl 4-(4-hydroxyphenyl)piperidine-1-carboxylate serves as a versatile building block for the synthesis of bioactive piperidine derivatives. The phenolic hydroxyl group enables direct functionalization or derivatization, while the tert-butoxycarbonyl (Boc) protecting group offers excellent bench stability and compatibility with standard deprotection protocols. It functions effectively in coupling reactions, Suzuki-Miyaura transformations, and as a scaffold for medicinal chemistry campaigns targeting CNS-active compounds and kinase inhibitors.
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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+P364-P405-P501
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Lot numbers can be found on the outside label of a product: