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Structure of 25128-32-9
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2,3-Dioxoindoline-5-carboxylic acid features a fused bicyclic core with two ketone groups and a carboxylic acid at the 5-position, enabling direct integration into heterocyclic scaffolds. The electron-deficient indoline framework supports nucleophilic additions and facilitates coupling reactions under mild conditions. This compound serves as a key intermediate in synthesizing bioactive molecules, particularly those requiring constrained, polarized ring systems for targeted binding.
2,3-Dioxoindoline-5-carboxylic acid serves as a versatile building block for the synthesis of indoline-based heterocycles and bioactive scaffolds. Its ortho-dicarbonyl motif enables facile functionalization via nucleophilic addition, condensation, or cyclization reactions. The carboxylic acid group provides a handle for derivatization and facilitates purification via ion-exchange chromatography. Bench-stable and compatible with standard reaction conditions, it functions effectively in medicinal chemistry campaigns targeting kinase inhibitors and CNS-active 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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: