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Structure of 458532-94-0
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This boronate moiety integrates readily into Suzuki-Miyaura cross-coupling reactions under standard conditions, delivering functionalized pyridyl architectures with high fidelity. The bromopyridine handle enables sequential diversification, while the bench-stable boronic acid group ensures reliable performance in iterative synthesis workflows.
(2-Bromopyridin-4-yl)boronic acid serves as a versatile building block in palladium-catalyzed cross-coupling reactions, enabling efficient C–C bond formation with aryl and vinyl halides. Its boronic acid functionality offers good bench stability and compatibility with diverse reaction conditions, while the pyridine ring provides orthogonal reactivity for further functionalization. This compound facilitates the construction of biaryl scaffolds commonly found in pharmaceutical intermediates and agrochemicals.
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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: