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Structure of 473416-33-0
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This boronate moiety integrates readily into Suzuki-Miyaura couplings, delivering functionalized fluoroaryl scaffolds with high efficiency. The electron-deficient aryl ring enhances reactivity while maintaining bench-stable handling under standard conditions.
(5-Fluorobenzofuran-2-yl)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 stability under ambient conditions and compatibility with diverse functional groups facilitate straightforward incorporation into complex molecular architectures. The fluorinated benzofuran scaffold provides enhanced metabolic stability and tunable electronic properties, making it a valuable component in the synthesis of bioactive molecules and pharmaceutical intermediates.
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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: