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Structure of 226396-32-3
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2,3,4-Trifluorophenylboronic acid features a trifluorinated aromatic ring that imparts enhanced stability and electron-deficient character, facilitating efficient cross-coupling reactions. This bench-stable reagent integrates readily into Suzuki-Miyaura protocols, enabling reliable C–C bond formation under mild conditions.
2,3,4-Trifluorophenylboronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation with aryl and vinyl halides. Its trifluorinated aryl framework imparts enhanced metabolic stability and lipophilicity, making it valuable for medicinal chemistry applications. The compound exhibits good bench stability, moderate reactivity, and compatibility with diverse functional groups, facilitating straightforward purification and integration into complex molecular architectures.
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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 : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: