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Structure of 661465-44-7
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Potassium (4-chlorophenyl)trifluoroborate delivers a stable, bench-ready boronate handle for Suzuki-Miyaura cross-coupling reactions. This electron-deficient aryl trifluoroborate integrates seamlessly into complex molecular architectures under standard conditions, offering enhanced functional group tolerance and predictable reactivity.
Potassium (4-chlorophenyl)trifluoroborate serves as a stable, bench-ready boron source for Suzuki-Miyaura cross-coupling reactions. Its ortho- and meta-substituted arylboronate functionality enables efficient C–C bond formation under mild conditions, with excellent functional group tolerance and predictable regiochemistry. The compound facilitates reliable synthesis of biaryl scaffolds commonly found in pharmaceutical intermediates and agrochemicals.
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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: