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Structure of 1266118-78-8
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tert-Butyl 4-(6-chloropyridin-2-yl)piperidine-1-carboxylate features a chloropyridine moiety linked to a piperidine scaffold, enabling direct incorporation into bioactive molecule synthesis. The tert-butyl ester group provides stability and facilitates straightforward deprotection under mild acidic conditions. This compound serves as a key intermediate in the development of kinase inhibitors and other pharmaceutical agents requiring a polar, electron-deficient heterocyclic core.
tert-Butyl 4-(6-chloropyridin-2-yl)piperidine-1-carboxylate serves as a versatile building block for the synthesis of bioactive heterocycles, enabling direct functionalization at the pyridine ring and piperidine nitrogen. The tert-butyl carbamate group offers excellent bench stability and facile removal under mild acidic conditions. Its compatibility with palladium-catalyzed cross-coupling reactions facilitates efficient construction of complex scaffolds relevant to medicinal chemistry and process development.
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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: