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Structure of 274257-34-0
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Potassium trifluoro(o-tolyl)borate delivers a sterically hindered, bench-stable boronate moiety ideal for Suzuki-Miyaura cross-coupling reactions. The ortho-methyl group enhances stability and modulates reactivity, enabling efficient C–C bond formation under standard conditions. This reagent integrates seamlessly into synthetic workflows requiring selective functionalization of aryl halides.
Potassium trifluoro(o-tolyl)borate serves as a stable, bench-friendly boron reagent enabling efficient Suzuki-Miyaura cross-coupling reactions. Its o-tolyl group provides enhanced stability and solubility in polar organic solvents, facilitating reliable C–C bond formation with aryl halides and pseudohalides. The trifluoroborate moiety ensures excellent functional group tolerance and predictable reactivity, making it ideal for constructing biaryl scaffolds in pharmaceutical and materials chemistry 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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: