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Structure of 903513-62-2
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This boronate moiety integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, delivering efficient access to functionalized heteroaryl scaffolds. The para-amino group enhances solubility and directs regioselective transformation, while the bench-stable boronic acid functionality enables reliable handling under standard conditions.
(2-Aminopyridin-4-yl)boronic acid serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl architectures. The pendant amine group offers orthogonal reactivity for further functionalization, while the boronic acid moiety provides excellent stability, ease of purification, and compatibility with standard Suzuki-Miyaura coupling conditions. Its robustness and predictable reactivity make it a reliable scaffold 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: