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Structure of 885693-20-9
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tert-Butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate integrates a boronate handle with a reducible dihydropyridine scaffold, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling. This bench-stable reagent facilitates the construction of complex nitrogen-containing architectures under mild conditions.
tert-Butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate serves as a stable, bench-ready building block for Suzuki-Miyaura coupling reactions. The boronate group enables efficient C–C bond formation under mild conditions, while the dihydropyridine core provides a versatile scaffold for further functionalization. Its tert-butyl ester functionality offers excellent stability and ease of purification, making it ideal for iterative synthesis in 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: