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Structure of 2438240-68-5
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This piperidine-2,6-dione scaffold features a 5-bromo-7-fluoro-1-oxoisoindolinyl group that imparts electron-withdrawing character and enhanced metabolic stability. The fused ring system enables robust integration into bioactive scaffolds, particularly in kinase inhibitor development. Bench-stable and compatible with standard coupling protocols, this compound serves as a key building block for medicinal chemistry campaigns requiring halogenated, sterically defined heterocycles.
3-(5-Bromo-7-fluoro-1-oxoisoindolin-2-yl)piperidine-2,6-dione serves as a versatile building block for isoindolinone-based scaffolds in medicinal chemistry. Its bromo and fluoro substituents enable downstream cross-coupling reactions, while the diketone functionality supports enolization and nucleophilic addition. The compound exhibits bench stability and facilitates efficient functional group manipulation, making it well-suited for parallel synthesis campaigns targeting bioactive heterocycles.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: