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Structure of 197958-29-5
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Pyridin-2-ylboronic acid delivers a pyridine-directed boronate handle for cross-coupling reactions. This bench-stable reagent integrates efficiently into Suzuki-Miyaura protocols, enabling direct functionalization at the pyridine nitrogen’s ortho position. The electron-deficient heterocycle enhances reactivity in palladium-catalyzed transformations while maintaining compatibility with diverse functional groups.
Pyridin-2-ylboronic acid serves as a versatile building block in cross-coupling chemistry, enabling efficient C–C bond formation via Suzuki-Miyaura reactions. Its pyridine functionality offers orthogonal reactivity and enhanced solubility compared to phenylboronic acids, while the boronic acid group provides reliable stability under standard bench conditions. This compound facilitates the construction of biaryl systems and heterocyclic scaffolds prevalent in pharmaceutical intermediates, with predictable coupling outcomes and straightforward purification.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: