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Structure of 1073339-21-5
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This boronate reagent features a trifluoromethyl-substituted aryl group paired with a sterically protected dioxaborolane ring, enabling stable coupling in Suzuki-Miyaura reactions. The electron-deficient phenyl moiety enhances reactivity while the tetramethyl substitution ensures bench-stable handling and resistance to protodeboronation.
4,4,5,5-Tetramethyl-2-(2-(trifluoromethyl)phenyl)-1,3,2-dioxaborolane serves as a stable, bench-ready boron reagent for palladium-catalyzed cross-coupling reactions. It enables efficient C–C bond formation with aryl and heteroaryl halides, offering enhanced functional group tolerance and compatibility with diverse reaction conditions. The trifluoromethyl-substituted arylboronate functions reliably in Suzuki-Miyaura coupling workflows, facilitating the construction of complex biaryl architectures common in pharmaceutical and agrochemical synthesis.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363
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Lot numbers can be found on the outside label of a product: