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Structure of 883231-20-7
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This boronate moiety integrates a tert-butoxycarbonyl-protected amine on a pyridine scaffold, enabling selective functionalization in late-stage diversification. The protected amine allows orthogonal reactivity, while the boronic acid group facilitates palladium-catalyzed cross-coupling under standard conditions. Bench-stable and moisture-tolerant, this building block supports efficient synthesis of bioactive heterocycles.
(6-((tert-Butoxycarbonyl)amino)pyridin-3-yl)boronic acid serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions with broad functional group tolerance. The protected amine moiety ensures stability during reaction conditions and facilitates selective deprotection post-coupling. Its pyridyl boronic acid framework supports efficient Suzuki-Miyaura coupling for constructing biaryl scaffolds, making it ideal for the synthesis of complex heterocyclic compounds and API intermediates.
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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: