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Structure of 659742-21-9
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2-Methylpyridine-5-boronic acid delivers a sterically accessible boronate handle tethered to a nitrogen-rich heterocycle, enabling efficient coupling in Suzuki-Miyaura reactions. The pyridyl scaffold enhances solubility and electronic tuning, while the methyl group provides steric differentiation. This bench-stable reagent streamlines access to functionalized aryl building blocks under standard conditions.
2-Methylpyridine-5-boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds. Its pyridyl boronic acid functionality exhibits good stability, ease of handling, and compatibility with diverse functional groups, facilitating straightforward purification and integration into complex molecular architectures common 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: