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Structure of 372963-50-3
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(6-Methylpyridin-2-yl)boronic acid features a pyridine ring bearing both a methyl group and a boronic acid moiety at adjacent positions, enabling efficient cross-coupling reactions. This bench-stable reagent integrates readily into Suzuki-Miyaura protocols, offering enhanced solubility and predictable reactivity in synthetic transformations.
(6-Methylpyridin-2-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. The pyridine moiety provides directional coordination and enhanced solubility, while the boronic acid group exhibits good bench stability and compatibility with diverse functional groups. It facilitates the synthesis of substituted heterocycles and biaryl scaffolds relevant to pharmaceutical development and materials chemistry.
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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: