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Structure of 911645-24-4
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This boronic acid features a trifluorinated aryl core with strategic chlorine and fluorine substituents, enabling efficient cross-coupling reactions. The electron-deficient ring enhances reactivity in Suzuki-Miyaura transformations, while the bench-stable nature simplifies handling and integration into complex synthetic sequences.
(5-Chloro-2,4-difluorophenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. Its ortho-fluoro and meta-chloro substituents enhance stability and modulate reactivity, while the boronic acid group offers excellent bench stability and ease of purification. Functions reliably in the construction of fluorinated aromatic scaffolds common in agrochemicals and pharmaceuticals.
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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: