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Structure of 886536-37-4
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This boronate moiety integrates a trifluoromethyl ether group, enhancing solubility and metabolic stability. The electron-withdrawing trifluoroethoxy substituent improves reaction efficiency in Suzuki-Miyaura couplings. Bench-stable under standard conditions, it enables reliable C–C bond formation with aryl halides and pseudohalides.
(4-(2,2,2-Trifluoroethoxy)phenyl)boronic acid serves as a stable, bench-ready building block for Suzuki-Miyaura cross-coupling reactions. Its trifluoroethoxy group enhances solubility and metabolic stability while maintaining compatibility with standard reaction conditions. The boronic acid moiety enables efficient C–C bond formation with aryl halides and pseudohalides, facilitating the construction of complex biaryl architectures relevant to 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-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: