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Structure of 2252415-10-2
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Potassium trifluoro(2-fluoro-6-hydroxyphenyl)borate features a boron center coordinated to a 2-fluoro-6-hydroxyphenyl group, enabling direct incorporation into Suzuki-Miyaura cross-coupling reactions. The hydroxyl functionality enhances solubility and facilitates derivatization, while the trifluoroborate moiety ensures stability under standard conditions. This reagent streamlines access to fluorinated aryl scaffolds in medicinal chemistry and materials science.
Potassium trifluoro(2-fluoro-6-hydroxyphenyl)borate serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. The ortho-fluoro and phenolic hydroxyl groups enable selective functionalization and in situ protection strategies, enhancing compatibility with diverse reaction conditions. Its high reactivity and tolerance to common functional groups facilitate efficient construction of biaryl architectures in medicinal chemistry and materials science applications.
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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+P364-P405-P501
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Lot numbers can be found on the outside label of a product: