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Structure of 2438241-40-6
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This piperidine-2,6-dione scaffold features a difluorinated isoindolinone moiety that enhances metabolic stability and modulates electronic properties. The fused ring system provides rigidity, enabling precise spatial orientation in target engagement. This structure serves as a key building block for bioactive molecules in medicinal chemistry, particularly in kinase inhibitor design and CNS-targeted drug discovery.
3-(5,6-Difluoro-1-oxoisoindolin-2-yl)piperidine-2,6-dione serves as a versatile building block for the synthesis of bioactive heterocycles, leveraging the electrophilic isoindolinone core and flanking amide functionalities. Its difluorinated aromatic system enhances metabolic stability and modulates electronic properties, while the piperidinedione scaffold offers orthogonal reactivity for downstream functionalization. The compound exhibits bench stability and facilitates efficient conjugation in multistep syntheses, enabling rapid access to complex scaffolds relevant to medicinal chemistry campaigns.
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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+P364-P405-P501
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Lot numbers can be found on the outside label of a product: