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Structure of 1217501-12-6
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This boronic acid features a strategically positioned bromo and fluoro substituent on the phenyl ring, enabling selective cross-coupling reactions. The electron-deficient aryl moiety enhances reactivity in palladium-catalyzed transformations, while the boronic acid group offers reliable coupling efficiency under standard conditions.
(2-Bromo-4-fluorophenyl)boronic acid serves as a versatile building block in palladium-catalyzed cross-coupling reactions, enabling efficient C–C bond formation with aryl halides and triflates. Its dual halogen functionality provides orthogonal reactivity for sequential transformations. The boronic acid moiety offers excellent stability under ambient conditions, facilitates straightforward purification, and exhibits broad functional group tolerance, making it well-suited for the synthesis of complex pharmaceutical intermediates and biaryl scaffolds.
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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: