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Structure of 1416990-09-4
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This piperidine-2,6-dione derivative features a hydroxyisoindolinone moiety that enhances solubility and enables hydrogen bonding in synthetic intermediates. The scaffold integrates robust stability with functional versatility for medicinal chemistry applications, particularly in kinase inhibitor design and peptide mimetics.
3-(6-Hydroxy-1-oxoisoindolin-2-yl)piperidine-2,6-dione serves as a versatile scaffold for constructing bioactive heterocycles, leveraging its dual functionality for orthogonal derivatization. The isoindolinone core enables facile functional group interconversions, while the piperidinedione moiety provides structural rigidity and hydrogen-bonding capacity. Bench-stable and amenable to standard purification methods, it facilitates efficient synthesis of complex molecular architectures in medicinal chemistry workflows.
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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: