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Structure of 2246602-45-7
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This pyrazole boronate ester integrates a sterically protected tetrahydro-pyran-4-yl group and a stable dioxaborolane moiety, enabling efficient Suzuki-Miyaura coupling under standard conditions. The 3,5-dimethyl substitution enhances solubility and stability, while the para-substituted arylboronate delivers predictable reactivity in cross-coupling workflows.
3,5-Dimethyl-1-(tetrahydro-2H-pyran-4-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. The tetrahydro-2H-pyran-4-yl group provides orthogonal protection and enhanced solubility, while the pinacol boronate moiety enables reliable coupling under mild conditions. This reagent facilitates efficient construction of complex pyrazole-based scaffolds with high functional group tolerance and predictable regiochemistry in medicinal chemistry and process R&D 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: