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Structure of 1310383-25-5
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This boronic acid features a trifluoromethyl group flanking a brominated aromatic ring, enabling efficient cross-coupling under standard conditions. The electron-deficient aryl moiety enhances reactivity in Suzuki-Miyaura processes, while the bench-stable boronate functionality simplifies handling and integration into complex molecular architectures.
(4-Bromo-3-(trifluoromethyl)phenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation with aryl, vinyl, and heteroaryl halides. The trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable for medicinal chemistry applications. Bench-stable and readily purified by recrystallization, it functions reliably in standard coupling protocols across diverse reaction conditions.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: