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Structure of 1083326-41-3
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This boronate-functionalized pyrazole acetic acid integrates readily into Suzuki-Miyaura coupling reactions under standard conditions. The tetramethyl-dioxaborolane moiety provides exceptional stability and moisture tolerance, enabling efficient cross-coupling with aryl halides. The pyrazole core offers a rigid, electron-rich platform ideal for bioactive molecule synthesis and probe development.
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-acetic acid serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The pyrazole acetic acid moiety provides enhanced solubility and functional group tolerance, enabling efficient incorporation into bioactive heterocyclic scaffolds. Bench-stable and compatible with standard reaction conditions, it facilitates rapid diversification in medicinal chemistry and materials synthesis workflows.
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Lot numbers can be found on the outside label of a product: