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Structure of 1049025-21-9
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tert-Butyl ((2-bromopyridin-4-yl)methyl)carbamate delivers a brominated pyridylmethyl scaffold with orthogonal protection, enabling direct functionalization at the pyridine ring. The carbamate group ensures stability during storage and facilitates selective deprotection under mild acidic conditions. This reagent streamlines access to advanced intermediates in medicinal chemistry campaigns involving nitrogen heterocycles.
tert-Butyl ((2-bromopyridin-4-yl)methyl)carbamate serves as a versatile building block for the synthesis of pyridyl-containing pharmaceutical intermediates. The bromine substituent enables palladium-catalyzed cross-coupling reactions, while the Boc-protected amine offers stability and ease of manipulation. This compound facilitates efficient access to functionalized heterocycles via standard deprotection and coupling protocols, making it well-suited for medicinal chemistry campaigns requiring late-stage diversification.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: