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Structure of 1197294-80-6
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tert-Butyl 4-(4-bromopyridin-2-yl)piperazine-1-carboxylate features a brominated pyridine moiety coupled to a piperazine scaffold, enabling direct integration into diverse synthetic pathways. The tert-butyl ester group provides stability and facilitates selective deprotection under mild acidic conditions. This compound serves as a key intermediate in the construction of bioactive heterocycles, particularly in medicinal chemistry campaigns targeting kinase inhibitors and CNS modulators.
tert-Butyl 4-(4-bromopyridin-2-yl)piperazine-1-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-containing scaffolds via Pd-catalyzed cross-coupling reactions. The pendant bromopyridine group facilitates Suzuki, Stille, and Negishi couplings, while the piperazine core offers a handle for further functionalization. The tert-butyl carbamate protection ensures stability during storage and handling, simplifying purification and integration into multi-step syntheses.
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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: