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Structure of 1187951-62-7
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Potassium trifluoro(4-phenoxyphenyl)borate delivers a stable, moisture-tolerant boron source for cross-coupling reactions. The electron-deficient trifluoroborate moiety enables efficient palladium-catalyzed transformations under mild conditions. This bench-stable reagent integrates seamlessly into synthetic workflows requiring high functional group tolerance and predictable reactivity.
Potassium trifluoro(4-phenoxyphenyl)borate serves as a stable, bench-ready boron source for Suzuki-Miyaura cross-coupling reactions. It facilitates efficient C–C bond formation with aryl and heteroaryl halides under mild conditions, offering excellent functional group tolerance and predictable regioselectivity. The phenoxy-substituted arylboron moiety enhances solubility and stability, enabling straightforward purification and reliable performance in 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-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: