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Structure of 1190235-39-2
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This tetramethylboronate integrates a trifluoromethyl-substituted benzyl group, offering enhanced stability and reactivity in cross-coupling processes. The sterically protected dioxaborolane core enables efficient Suzuki-Miyaura reactions under standard conditions.
4,4,5,5-Tetramethyl-2-(3-(trifluoromethyl)benzyl)-1,3,2-dioxaborolane serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. The trifluoromethyl-substituted benzyl group provides enhanced metabolic stability and lipophilicity, making it valuable for constructing biologically relevant scaffolds. Its high functional group tolerance and ease of purification enable reliable integration into complex molecule 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-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: