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Structure of 1184950-48-8
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tert-Butyl 3-bromo-5,6,7,8-tetrahydro-1,6-naphthyridine-6-carboxylate features a brominated tetrahydronaphthyridine core with a bench-stable tert-butyl ester handle. This electron-deficient heterocycle integrates readily into cross-coupling reactions, enabling efficient access to functionalized naphthyridine scaffolds for medicinal chemistry and materials applications.
tert-Butyl 3-bromo-5,6,7,8-tetrahydro-1,6-naphthyridine-6-carboxylate serves as a versatile building block for the synthesis of biologically relevant tetrahydronaphthyridine scaffolds. The bromo group enables palladium-catalyzed cross-coupling reactions, while the tert-butyl ester offers stability and convenient deprotection under mild acidic conditions. Its functional group tolerance and bench stability facilitate efficient access to diverse heterocyclic architectures in medicinal chemistry and process development workflows.
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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: