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Structure of 913836-15-4
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This boronate moiety features a chlorine-substituted pyridine core, enabling efficient coupling in Suzuki-Miyaura reactions. The methyl group enhances regioselectivity and stability under standard conditions, while the boronic acid functionality offers reliable reactivity and bench-stable handling for synthetic applications.
(6-Chloro-2-methylpyridin-3-yl)boronic acid serves as a versatile building block in palladium-catalyzed cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl architectures. The ortho-chloro substituent provides a handle for downstream functionalization via nucleophilic substitution or further coupling, while the boronic acid group offers excellent bench stability and compatibility with standard Suzuki-Miyaura conditions. Its defined regiochemistry and predictable reactivity make it a reliable scaffold for medicinal chemistry and materials synthesis.
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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: