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Structure of 913836-08-5
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2-Chloro-4-methyl-5-pyridineboronic acid features a pyridine scaffold with strategically positioned boronic acid and chloro substituents, enabling direct coupling in palladium-catalyzed cross-coupling reactions. The electron-deficient pyridine ring enhances reactivity, while the methyl group provides steric control. This bench-stable reagent integrates efficiently into complex molecular architectures.
2-Chloro-4-methyl-5-pyridineboronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds. Its pyridine core provides orthogonal reactivity, while the boronic acid group offers excellent bench stability and compatibility with diverse functional groups. The chloro and methyl substituents facilitate downstream derivatization, making this compound a practical choice for medicinal chemistry and process development workflows.
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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: