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Structure of 247564-72-3
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2,4,5-Trifluorophenylboronic acid features a trifluorinated aromatic ring that enhances electronic withdrawal and metabolic stability. This electron-deficient boronate moiety integrates efficiently into Suzuki-Miyaura coupling reactions under standard conditions. The compound exhibits bench-stable handling characteristics and delivers high functional group tolerance in complex molecule assembly.
2,4,5-Trifluorophenylboronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. Its trifluorinated aryl scaffold offers enhanced metabolic stability and improved lipophilicity, making it valuable for medicinal chemistry applications. The boronic acid exhibits excellent bench stability, facilitates straightforward purification, and demonstrates broad functional group tolerance in diverse synthetic 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 : 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: