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Structure of 652148-97-5
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5-Bromopyridin-2-ylboronic acid features a pyridine ring bearing both bromo and boronic acid functionalities at adjacent positions. This dual-functionalized scaffold enables direct coupling in Suzuki-Miyaura reactions, delivering substituted pyridines with high efficiency. The boronic acid group exhibits excellent stability under standard conditions, while the bromo substituent serves as a complementary handle for cross-coupling or further functionalization.
5-Bromopyridin-2-ylboronic 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 bromine and boronic acid functionalities offer orthogonal reactivity for sequential transformations. The compound exhibits good bench stability, ease of handling, and compatibility with diverse reaction conditions, facilitating the construction of complex heterocyclic scaffolds common in medicinal chemistry and materials science.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: