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Structure of 1049730-42-8
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This pyrazole boronate ester integrates a trifluoroethyl group and a tetramethyl-1,3,2-dioxaborolane moiety, enabling stable coupling under standard conditions. The electron-deficient pyrazole ring enhances reactivity in Suzuki-Miyaura cross-coupling, while the sterically protected boronate ensures shelf stability and compatibility with diverse functional groups.
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-(2,2,2-trifluoroethyl)-1H-pyrazole serves as a versatile boron-containing building block for Suzuki-Miyaura cross-coupling reactions. The pyrazole core provides metabolic stability and favorable pharmacophore properties, while the trifluoroethyl group enhances lipophilicity and bioavailability. The boronic ester functionality enables reliable coupling under mild conditions, with excellent bench stability and compatibility with diverse functional groups, facilitating efficient assembly of complex heterocyclic scaffolds in medicinal chemistry and process development 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-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: