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Structure of 374930-88-8
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tert-Butyl 4-(5-bromopyrimidin-2-yl)piperazine-1-carboxylate features a brominated pyrimidine moiety linked to a piperazine scaffold, enabling direct incorporation into medicinal chemistry campaigns. This bench-stable building block delivers efficient access to kinase inhibitors and other bioactive heterocycles through palladium-catalyzed cross-coupling reactions.
tert-Butyl 4-(5-bromopyrimidin-2-yl)piperazine-1-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrimidine-containing scaffolds. The bromine substituent facilitates palladium-catalyzed cross-coupling reactions, while the tert-butyl piperazine carboxylate group offers stability and convenient deprotection under mild acidic conditions. Its functional group tolerance supports integration into complex molecules for drug discovery applications.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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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: