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Structure of 1002334-12-4
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1-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole features a boronate ester group that enables efficient Suzuki-Miyaura cross-coupling reactions. The pyrazole core provides structural rigidity and electronic stability, while the tetramethyl-substituted dioxaborolane enhances moisture tolerance and shelf life. This compound integrates readily into complex molecular architectures under standard conditions.
1-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole serves as a versatile boron-containing building block for Suzuki-Miyaura cross-coupling reactions. The pyrazole core provides metabolic stability and hydrogen-bonding capacity, while the pinacol boronate ester enables efficient, mild coupling with aryl and heteroaryl halides. Bench-stable and compatible with diverse functional groups, it facilitates rapid access to biaryl-pyrazole scaffolds prevalent in medicinal chemistry and agrochemical research.
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Lot numbers can be found on the outside label of a product: