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Structure of 937595-70-5
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This boronate moiety features a chloro-fluoro substitution pattern on the pyridine ring, delivering enhanced stability and reactivity in cross-coupling processes. The electron-deficient heterocycle enables efficient palladium-catalyzed transformations under standard conditions.
(5-Chloro-2-fluoropyridin-3-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. Its compatibility with diverse functional groups and bench-stable nature facilitate reliable incorporation into complex molecular architectures. The ortho-fluoro and meta-chloro substituents provide strategic reactivity for further derivatization, making it a valuable scaffold in the synthesis of pharmaceutical intermediates and agrochemical candidates.
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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: