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Structure of 1375452-67-7
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This boronate moiety integrates a pyridine-based scaffold with an aminomethyl handle, enabling efficient coupling in transition-metal-catalyzed transformations. The pendant amine facilitates purification and functionalization, while the boronic acid group delivers high reactivity under mild conditions. Bench-stable and moisture-tolerant, this reagent streamlines access to bioactive heterocycles in medicinal chemistry workflows.
(6-(Aminomethyl)pyridin-3-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under mild conditions. The pendant amine group provides orthogonal functionality for further derivatization, while the boronic acid moiety offers excellent bench stability and compatibility with diverse reaction partners. Its utility is well-established in constructing bioactive heterocyclic scaffolds and functionalized aryl systems.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: