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Structure of 943153-22-8
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This boronate moiety features a chlorinated pyridine core with a methoxy substituent, enabling selective coupling in Suzuki-Miyaura reactions. The electron-deficient heterocycle enhances reactivity while maintaining bench-stable handling under standard conditions.
(5-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 scaffolds. The chloropyridine core provides orthogonal reactivity for further functionalization, while the boronic acid group offers excellent stability, ease of handling, and compatibility with standard Suzuki-Miyaura coupling conditions. Its methoxy substituent enhances solubility and modulates electronic properties, facilitating downstream derivatization in medicinal chemistry and materials science applications.
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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: