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Structure of 943323-55-5
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4-Bromo-1H-pyrrolo[2,3-b]pyridin-6-amine features a brominated pyrrolopyridine core with a pendant amine group, enabling direct functionalization in C–N cross-coupling reactions. The electron-deficient heteroaromatic scaffold supports palladium-catalyzed transformations, while the amine moiety serves as a handle for derivatization. This compound offers high reactivity and bench stability under standard conditions.
4-Bromo-1H-pyrrolo[2,3-b]pyridin-6-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its bromo-substituted heterocyclic core. The pyrrolo[2,3-b]pyridine scaffold provides enhanced metabolic stability and favorable pharmacophore properties, while the primary amine functionality supports direct derivatization or conjugation. Bench-stable and readily purified, it facilitates efficient synthesis of complex nitrogen-containing scaffolds for drug discovery applications.
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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: