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Structure of 496786-98-2
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tert-Butyl 4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)piperazine-1-carboxylate features a boronate ester group enabling robust Suzuki-Miyaura coupling. The piperazine scaffold provides a versatile nitrogen-rich platform for diversification. Bench-stable and moisture-tolerant, this reagent streamlines access to complex pyridyl-piperazine architectures in medicinal chemistry and materials science.
tert-Butyl 4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)piperazine-1-carboxylate serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The piperazine moiety provides a polar, basic nitrogen scaffold useful in medicinal chemistry, while the tert-butyl carbamate offers stability and ease of removal under mild acidic conditions. Functional group tolerance enables reliable coupling with diverse aryl and heteroaryl halides, facilitating rapid access to complex molecular architectures in drug discovery 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: