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Structure of 374564-35-9
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Potassium (4-bromophenyl)trifluoroborate delivers a stable, bench-ready boronate handle for Suzuki-Miyaura cross-coupling reactions. This moisture-tolerant reagent integrates seamlessly into synthetic workflows, enabling efficient C–C bond formation under mild conditions. The para-brominated aryl trifluoroborate combines high functional group compatibility with predictable reactivity, streamlining access to complex biaryl architectures in pharmaceutical and materials synthesis.
Potassium (4-bromophenyl)trifluoroborate serves as a stable, bench-ready boron reagent for palladium-catalyzed cross-coupling reactions. It facilitates efficient Suzuki-Miyaura coupling with aryl and heteroaryl halides, offering excellent functional group tolerance and reliable yields. The trifluoroborate moiety enhances stability and solubility compared to traditional boronic acids, enabling straightforward handling and purification in synthetic workflows.
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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: