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Structure of 2304513-76-4
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This piperidine-2,6-dione scaffold features a brominated isoindolinone moiety, delivering enhanced reactivity and stability for synthetic applications. The electron-deficient ring system enables efficient coupling in transition-metal-catalyzed transformations, while the sterically accessible core facilitates modular derivatization. Designed for robust performance under standard conditions, this compound serves as a key intermediate in medicinal chemistry campaigns targeting bioactive heterocycles.
3-(6-Bromo-1-oxoisoindolin-2-yl)piperidine-2,6-dione serves as a versatile building block for the synthesis of isoindolinone-based scaffolds prevalent in medicinal chemistry. The bromo substituent enables palladium-catalyzed cross-coupling reactions, while the diketone functionality supports enolization and condensation processes. Its bench-stable solid form and compatibility with diverse reaction conditions facilitate efficient integration into multi-step syntheses of bioactive compounds.
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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: