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Structure of 579476-63-4
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This boronate moiety integrates readily into Suzuki-Miyaura cross-coupling reactions under standard conditions, delivering functionalized heteroaryl products with high efficiency. The 2-methylpyridin-4-yl scaffold provides enhanced stability and favorable electronic properties for transition-metal catalysis.
(2-Methylpyridin-4-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. Its pyridyl boronic acid functionality exhibits excellent bench stability and compatibility with diverse functional groups, facilitating the construction of biaryl scaffolds prevalent in pharmaceutical and agrochemical research. The methyl substituent enhances solubility and modulates electronic properties, improving reactivity in standard coupling protocols.
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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: