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Structure of 1072946-66-7
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This boronate moiety enables efficient coupling in Suzuki-Miyaura reactions, delivering functionalized heterocycles with high regioselectivity. The chloro and fluoro substituents provide orthogonal reactivity, enhancing synthetic versatility in medicinal chemistry and materials science applications.
(6-Chloro-5-fluoropyridin-3-yl)boronic acid serves as a versatile building block in palladium-catalyzed cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds. Its orthogonal reactivity profile—where the chloro and fluoro groups permit selective functionalization—facilitates downstream derivatization in medicinal chemistry and agrochemical synthesis. The boronic acid moiety exhibits excellent bench stability and compatibility with standard Suzuki-Miyaura coupling conditions, simplifying purification and scale-up.
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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: