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Structure of 1391926-50-3
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tert-Butyl 4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine-1-carboxylate features a boronate ester group enabling efficient Suzuki-Miyaura coupling. The pyrrolo[2,3-b]pyridine core provides a rigid, electron-deficient scaffold suitable for C–C bond formation in complex molecule assembly. Bench-stable and moisture-tolerant, this reagent integrates seamlessly into synthetic workflows requiring precise functionalization.
tert-Butyl 4-(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 pyrrolo[2,3-b]pyridine core provides a rigid, nitrogen-rich scaffold relevant to medicinal chemistry, while the boronic ester functionality enables efficient C–C bond formation under mild conditions. Bench-stable and compatible with diverse reaction partners, it facilitates rapid access to complex heterocyclic architectures in drug discovery and materials science 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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: