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Structure of 1072946-50-9
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This boronate moiety features a chlorine-substituted pyridine core with a methoxy group at the 2-position, delivering enhanced stability and selective reactivity in cross-coupling processes. The electron-deficient heteroaromatic scaffold enables efficient palladium-catalyzed transformations under standard conditions.
(6-Chloro-2-methoxypyridin-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 chloropyridine moiety supports orthogonal functionalization, while the boronic acid group offers excellent bench stability and compatibility with Suzuki-Miyaura coupling conditions. Its methoxy substituent enhances solubility and modulates electronic properties, facilitating downstream derivatization in 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: