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Structure of 2408391-89-7
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This piperidine-2,6-dione scaffold features a bromo-fluoro-substituted isoindolinone core, delivering enhanced electron-withdrawing character and steric profile. The functionalized heterocycle enables direct integration into complex molecular architectures under standard conditions.
3-(5-Bromo-4-fluoro-1-oxoisoindolin-2-yl)piperidine-2,6-dione serves as a versatile building block for the synthesis of isoindolinone-based scaffolds. Its bromo and fluoro substituents enable late-stage functionalization via palladium-catalyzed cross-coupling reactions. The diketone functionality provides access to diverse heterocyclic systems and supports conjugation with biologically relevant moieties, offering robust utility in medicinal chemistry campaigns requiring stable, modular intermediates.
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GHS Pictogram :
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GHS No : GHS08
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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 : H361
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Precautionary Statements : P280-P405-P501
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Lot numbers can be found on the outside label of a product: