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Structure of 874290-88-7
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This boronate moiety integrates seamlessly into Suzuki-Miyaura couplings, offering enhanced stability and solubility under standard conditions. The electron-deficient pyridine ring facilitates selective reaction pathways, while the cyanide group enables downstream functionalization through nucleophilic addition or metal-catalyzed transformations.
(2-Cyanopyridin-3-yl)boronic acid serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient access to functionalized pyridine scaffolds. Its cyano group provides enhanced electronic modulation and orthogonal reactivity, while the boronic acid moiety offers excellent bench stability and compatibility with Suzuki-Miyaura coupling protocols. The compound facilitates rapid diversification of heterocyclic systems in medicinal chemistry and materials science applications.
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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: