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Structure of 1047644-76-7
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This boronate-functional pyrazole integrates seamlessly into Suzuki-Miyaura coupling reactions, offering high stability under standard conditions. The tetramethyl-dioxaborolane moiety enables efficient cross-coupling, while the methyl substituents enhance solubility and reduce aggregation. A robust, bench-stable reagent for constructing complex heterocyclic architectures in medicinal chemistry and materials science.
1,4-Dimethyl-5-(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 tetramethyl dioxaborolane group enables reliable C–C bond formation under mild conditions, while the pyrazole core provides a rigid, electron-deficient heterocyclic scaffold with demonstrated utility in medicinal chemistry and materials science applications. Functional group tolerance and ease of purification support its integration into complex molecular architectures.
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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-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: