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Structure of 847818-55-7
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This boronate moiety integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, delivering high functional group tolerance and stability under standard conditions. The methylated pyrazole scaffold enhances solubility and resistance to protodeboronation, enabling efficient derivatization in synthetic workflows.
(1-Methyl-1H-pyrazol-4-yl)boronic acid serves as a robust boronate building block for Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. Its pyrazole core imparts enhanced stability and solubility, while the methyl group improves functional group tolerance and facilitates purification. Widely used in medicinal chemistry and agrochemical synthesis, it functions reliably in the construction of biologically relevant heterocyclic scaffolds.
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Lot numbers can be found on the outside label of a product: