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Structure of 1188477-11-3
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tert-Butyl ((5-bromopyridin-2-yl)methyl)carbamate delivers a brominated pyridyl methyl scaffold with orthogonal protection, enabling direct functionalization at the 5-position. This bench-stable reagent integrates readily into cross-coupling workflows, where the carbamate group facilitates purification and selective deprotection.
tert-Butyl ((5-bromopyridin-2-yl)methyl)carbamate serves as a versatile building block in medicinal chemistry, enabling the efficient introduction of a brominated pyridine moiety via orthogonal N-Boc deprotection. Its stability under standard reaction conditions and compatibility with palladium-catalyzed cross-coupling reactions facilitate rapid access to functionalized heterocycles. The Boc-protected amine allows for selective transformations, while the pendant bromide supports diverse late-stage modifications, making it ideal for scaffold diversification in API 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-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: