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Structure of 149142-67-6
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5-Bromo-1H-pyrrolo[2,3-b]pyridine-2,3-dione features a rigid, electron-deficient heterocyclic core with dual carbonyl groups and a bromine substituent at the 5-position. This configuration enables direct functionalization in cross-coupling reactions and facilitates integration into advanced scaffolds for medicinal chemistry and materials development.
5-Bromo-1H-pyrrolo[2,3-b]pyridine-2,3-dione serves as a versatile building block in the synthesis of heterocyclic scaffolds, enabling efficient access to complex nitrogen-containing frameworks. Its bromine substituent facilitates palladium-catalyzed cross-coupling reactions, while the fused diketone system provides sites for selective functionalization. The compound exhibits good bench stability and is compatible with standard synthetic workflows, supporting its use in medicinal chemistry and materials science 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: