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Structure of 1072951-50-8
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This boronic acid features a trifluoromethyl group that enhances electron deficiency and stability, enabling efficient Suzuki-Miyaura coupling under standard conditions. The ortho-hydroxyl moiety promotes in situ activation and improves solubility in polar solvents, facilitating reaction progress in aqueous or mixed media.
(2-Hydroxy-4-(trifluoromethyl)phenyl)boronic acid serves as a versatile building block for the synthesis of biaryl and heterocyclic scaffolds via palladium-catalyzed cross-coupling reactions. The ortho-hydroxyl group enables intramolecular coordination, enhancing reactivity in Suzuki-Miyaura couplings while maintaining bench stability and compatibility with diverse functional groups. Its trifluoromethyl substituent imparts enhanced metabolic stability and lipophilicity, making it valuable for medicinal chemistry applications requiring robust, electron-deficient aryl units.
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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-H335
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Precautionary Statements : P233-P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: