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Structure of 57583-53-6
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This electron-deficient heterocycle features four carbonyl groups arranged for enhanced reactivity in C–H functionalization. The two hydroxyl substituents at the 2- and 6-positions enable intramolecular hydrogen bonding, stabilizing reactive intermediates. Designed for use in advanced synthetic sequences requiring high regiocontrol.
2,6-Dihydroxypyrrolo[3,4-f]isoindole-1,3,5,7(2H,6H)-tetraone serves as a versatile heterocyclic building block for the synthesis of complex polycyclic scaffolds. Its four ketone functionalities and phenolic hydroxyl groups enable sequential functionalization and serve as handles for derivatization via condensation, reduction, or metal-catalyzed coupling reactions. The molecule exhibits bench stability and facilitates purification by crystallization, making it suitable for use in medicinal chemistry campaigns targeting kinase inhibitors and other bioactive compounds.
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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+P364
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Lot numbers can be found on the outside label of a product: