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Structure of 2248620-18-8
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Potassium trifluoro(2-(trifluoromethyl)benzyl)borate delivers a sterically accessible boronate handle with enhanced stability and solubility in polar solvents. This bench-stable reagent enables direct C–H functionalization and Suzuki–Miyaura coupling under mild conditions, leveraging the electron-deficient aryl framework for efficient cross-coupling with diverse partners.
Potassium trifluoro(2-(trifluoromethyl)benzyl)borate serves as a stable, bench-friendly boron reagent enabling efficient Suzuki-Miyaura cross-coupling reactions. Its trifluoromethyl-substituted benzyl group confers enhanced functional group tolerance and improved oxidative stability, facilitating reliable C–C bond formation under standard catalytic conditions. This reagent functions effectively in the construction of biaryl scaffolds and complex heterocycles relevant to pharmaceutical 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 : 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: