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Structure of 1453799-69-3
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This tetrahydro-pyrrolopyridinone scaffold features a brominated position at C2, enabling direct functionalization in late-stage diversification. The electron-deficient core supports efficient cross-coupling reactions under mild conditions, while the lactam carbonyl enhances solubility and enables hydrogen bonding in synthetic intermediates.
2-Bromo-1,5,6,7-tetrahydro-4H-pyrrolo[3,2-c]pyridin-4-one serves as a versatile building block for the synthesis of nitrogen-containing heterocycles and bioactive scaffolds. The bromine atom enables palladium-catalyzed cross-coupling reactions, while the pyrrolopyridinone core provides a rigid, electron-deficient platform compatible with diverse functional group transformations. Its bench-stable nature and ease of purification facilitate integration into medicinal chemistry workflows and process-scale applications.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501
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Lot numbers can be found on the outside label of a product: