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Structure of 1417985-25-1
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This boronate moiety integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, delivering functionalized heterocycles with high efficiency. The pyrazolopyridine scaffold offers enhanced stability and solubility under standard conditions, enabling robust coupling in complex molecular architectures.
(1H-Pyrazolo[3,4-b]pyridin-5-yl)boronic acid serves as a versatile building block for constructing biologically relevant heterocyclic scaffolds. Its boronic acid functionality enables reliable Suzuki-Miyaura cross-coupling reactions under mild conditions, facilitating the synthesis of complex pyrazolo-pyridine derivatives. The compound exhibits good bench stability and functional group tolerance, supporting efficient purification and integration into iterative synthetic sequences common in medicinal chemistry and process development workflows.
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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: