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Structure of 1190322-18-9
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5-Bromo-1H-pyrrolo[2,3-b]pyridin-6-amine features a brominated pyrrolopyridine core with a pendant amine group, enabling direct functionalization in cross-coupling and bioconjugation workflows. The electron-deficient heterocycle facilitates palladium-catalyzed transformations, while the amine moiety offers versatility for derivatization. This scaffold demonstrates stability under standard conditions and compatibility with diverse reaction environments.
5-Bromo-1H-pyrrolo[2,3-b]pyridin-6-amine serves as a versatile building block in medicinal chemistry, enabling direct functionalization via Pd-catalyzed cross-coupling reactions. The bromine and amine groups provide orthogonal reactivity for sequential derivatization, while the fused heterocyclic core offers enhanced metabolic stability. Bench-stable and readily purified by recrystallization, it facilitates efficient access to complex pyrrolopyridine scaffolds common in kinase inhibitors and CNS-targeted therapeutics.
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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: