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Structure of 936250-20-3
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3-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole features a boronate ester group enabling efficient Suzuki-Miyaura cross-coupling under mild conditions. The tetramethyl-substituted dioxaborolane enhances stability and solubility in organic solvents. This pyrazole derivative integrates readily into complex molecular architectures, offering a robust handle for C–C bond formation in medicinal chemistry and materials synthesis.
3-Methyl-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 tetramethylboronate group enables efficient, mild coupling with aryl and heteroaryl halides, while the pyrazole core provides a stable, electron-rich scaffold. Bench-stable and readily purified by flash chromatography, it facilitates rapid access to functionalized pyrazole derivatives in medicinal chemistry and materials science applications.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: