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Structure of 908369-20-0
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This boronate moiety integrates a hydroxymethyl-functionalized pyridine scaffold, enabling efficient coupling in Suzuki-Miyaura reactions. The pendant hydroxyl group enhances solubility and facilitates downstream derivatization, while the pyridine nitrogen provides directional coordination in transition-metal-catalyzed transformations. Bench-stable under standard conditions, this reagent streamlines access to functionalized heteroaromatics.
(5-(Hydroxymethyl)pyridin-3-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds. The pyridine core provides orthogonal reactivity for downstream functionalization, while the boronic acid moiety offers excellent bench stability and compatibility with diverse reaction conditions. Its hydroxymethyl group enhances solubility and facilitates further derivatization, making it 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: