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Structure of 374538-01-9
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B-(4-Fluoro-3-formylphenyl)boronic acid features a boronic acid moiety paired with an electron-deficient fluoro-substituted aldehyde-bearing aryl ring, enabling efficient Suzuki-Miyaura coupling and direct functionalization. This bench-stable reagent integrates seamlessly into complex molecular architectures requiring orthogonal reactivity.
B-(4-Fluoro-3-formylphenyl)boronic acid serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient C–C bond formation with aryl halides and triflates. The ortho-fluoro and aldehyde functionalities provide orthogonal reactivity for downstream derivatization, including nucleophilic addition and oxime formation. Its bench-stable nature and compatibility with standard Suzuki-Miyaura conditions make it ideal for constructing complex aromatic scaffolds in medicinal chemistry and materials science applications.
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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: