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Structure of 2229976-08-1
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This piperidine-2,6-dione scaffold features a brominated isoindolinone moiety, enabling direct integration into complex molecular architectures. The electron-deficient ring system supports efficient coupling reactions, while the sterically accessible piperidine nitrogen facilitates functionalization. Bench-stable and moisture-tolerant, this compound streamlines access to advanced intermediates in medicinal chemistry and materials synthesis.
3-(7-Bromo-1-oxoisoindolin-2-yl)piperidine-2,6-dione serves as a versatile building block for the synthesis of isoindoline-based heterocycles and bioactive scaffolds. Its brominated isoindolinone moiety enables facile late-stage functionalization via cross-coupling reactions, while the piperidine-2,6-dione core provides a rigid, electron-deficient framework compatible with diverse transformations. The compound exhibits excellent bench stability and facilitates efficient purification, making it well-suited for medicinal chemistry campaigns and process-scale 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-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: