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Structure of 69807-91-6
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This boronate-functionalized benzene derivative integrates a trifluoromethyl-rich aromatic core with a stable, moisture-tolerant dioxaborolane handle. The para-substituted boronate moiety enables efficient Suzuki-Miyaura cross-coupling under standard conditions, while the electron-deficient framework enhances reactivity in transition-metal-catalyzed transformations.
1,3-Bis(trifluoromethyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The tetramethylboronate moiety enables efficient coupling with aryl halides under mild conditions, while the electron-withdrawing trifluoromethyl groups enhance stability and modulate reactivity. Its bench-stable solid form facilitates handling and purification, making it well-suited for constructing complex aromatic scaffolds 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 : 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: