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Structure of 361550-43-8
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tert-Butyl 5-bromopyridin-3-ylcarbamate features a brominated pyridine core with a tert-butyl carbamate protecting group, enabling selective functionalization in late-stage diversification. The electron-deficient pyridine ring facilitates cross-coupling reactions, while the bench-stable carbamate moiety allows for straightforward deprotection under mild acidic conditions. This combination supports efficient access to biologically relevant scaffolds in medicinal chemistry and materials synthesis.
tert-Butyl 5-bromopyridin-3-ylcarbamate serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the pyridine C5 position via palladium-catalyzed cross-coupling reactions. The tert-butyl carbamate group provides excellent stability and facilitates straightforward deprotection under mild acidic conditions. Its bromo substituent offers high reactivity in Suzuki, Stille, and Negishi couplings, while maintaining compatibility with diverse functional groups commonly encountered in API synthesis.
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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: