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Structure of 1190322-13-4
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4,6-Dichloro-1H-pyrrolo[2,3-b]pyridin-2(3H)-one is a chlorinated heterocyclic scaffold featuring two electron-withdrawing chlorine substituents at the 4 and 6 positions. This configuration enhances electrophilicity at the C2 carbonyl carbon, enabling efficient coupling reactions in late-stage functionalization. The compound exhibits bench-stable behavior and tolerates a range of reaction conditions, making it valuable for medicinal chemistry and materials synthesis.
4,6-Dichloro-1H-pyrrolo[2,3-b]pyridin-2(3H)-one serves as a versatile building block for constructing biologically relevant heterocyclic scaffolds. The dichloro substitution pattern enables selective functionalization via palladium-catalyzed cross-coupling reactions, while the pyrrolopyridinone core exhibits favorable bench stability and compatibility with common protecting group strategies. Its reactivity profile facilitates efficient access to substituted analogs in medicinal chemistry campaigns.
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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: