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Structure of 1370616-23-1
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tert-Butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine-1-carboxylate features a boronate ester group that enables efficient Suzuki-Miyaura coupling under mild conditions. This bench-stable reagent integrates seamlessly into complex molecule assembly, particularly in medicinal chemistry and heterocyclic synthesis workflows.
tert-Butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine-1-carboxylate serves as a versatile boron-containing building block for palladium-catalyzed cross-coupling reactions. The stable pinacol boronate group enables efficient Suzuki-Miyaura coupling with aryl and heteroaryl halides, while the pyrrolo[2,3-b]pyridine core provides a rigid, electron-deficient scaffold relevant to medicinal chemistry. Bench-stable and readily purified by flash chromatography, it facilitates the rapid assembly of complex heterocyclic architectures.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: