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Structure of 325786-27-4
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This boronic acid features a trifunctional aryl scaffold with chloro, fluoro, and formyl groups positioned ortho to the boronic acid moiety. The electron-deficient ring enhances reactivity in Suzuki-Miyaura coupling, while the formyl group enables downstream functionalization. Bench-stable under standard conditions, it facilitates efficient access to complex heterocycles and pharmaceutical intermediates.
(4-Chloro-2-fluoro-5-formylphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling the construction of complex arylated scaffolds with high functional group tolerance. The formyl group provides additional site for downstream derivatization, while the boronic acid moiety offers excellent bench stability and ease of purification. This reagent facilitates efficient access to substituted heterocycles and biaryl architectures relevant to medicinal chemistry and materials science.
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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: