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Structure of 864266-29-5
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tert-Butyl ((6-bromopyridin-3-yl)methyl)carbamate features a brominated pyridine scaffold with a stable, moisture-tolerant carbamate protecting group. This bench-stable reagent integrates readily into cross-coupling workflows, enabling efficient access to functionalized heterocycles through Pd-catalyzed transformations. The para-brominated site facilitates selective derivatization in complex molecular architectures.
tert-Butyl ((6-bromopyridin-3-yl)methyl)carbamate serves as a versatile building block in medicinal chemistry, enabling the efficient construction of pyridine-based scaffolds. The bromine substituent facilitates palladium-catalyzed cross-coupling reactions, while the tert-butyl carbamate group provides stable nitrogen protection under standard reaction conditions. This compound exhibits excellent bench stability and simplifies purification due to its low polarity and resistance to hydrolysis, making it ideal for multi-step synthesis workflows requiring orthogonal functional group handling.
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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: