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Structure of 1061604-41-8
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This piperidine-2,6-dione derivative features a hydroxyisoindolinone moiety that enhances solubility and enables selective bioconjugation. The scaffold integrates a sterically hindered amide linkage and electron-deficient aromatic system, supporting stability under standard conditions. Designed for use in targeted drug delivery systems and medicinal chemistry libraries, it facilitates efficient coupling reactions without requiring extensive purification.
3-(4-Hydroxy-1-oxoisoindolin-2-yl)piperidine-2,6-dione serves as a versatile scaffold for medicinal chemistry campaigns, enabling efficient access to complex heterocyclic architectures. The molecule combines a hydroxylated isoindolinone core with a diketopiperazine moiety, offering multiple sites for derivatization. Its bench-stable nature and compatibility with standard coupling reactions facilitate rapid analog synthesis. Functions effectively in the construction of bioactive molecules requiring fused ring systems and hydrogen-bonding capabilities.
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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-H312-H315-H319
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: