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Structure of 1394346-22-5
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This boronate moiety features a para-brominated trifluoromethylated aryl group, delivering enhanced stability and compatibility in Suzuki-Miyaura cross-coupling reactions. The electron-deficient ring facilitates efficient palladium-catalyzed bond formation, enabling rapid access to complex heteroaryl architectures under standard conditions.
(4-Bromo-2-(trifluoromethyl)phenyl)boronic acid serves as a versatile building block in palladium-catalyzed cross-coupling reactions, enabling efficient C–C bond formation under standard Suzuki-Miyaura conditions. Its stability, compatibility with diverse functional groups, and predictable reactivity make it ideal for constructing complex aryl 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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
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Lot numbers can be found on the outside label of a product: