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Structure of 14192-26-8
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Methyl 2-oxoindoline-6-carboxylate features a fused indoline core with a ketone and ester at the 2- and 6-positions, respectively. This electron-deficient scaffold integrates readily into heterocyclic synthesis, serving as a key intermediate for bioactive alkaloids and pharmaceuticals. The molecule exhibits bench-stable handling and compatibility with diverse coupling reactions under standard conditions.
Methyl 2-oxoindoline-6-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to indoline-based scaffolds prevalent in bioactive molecules. Its conjugated carbonyl system and ester functionality support diverse transformations, including reductive amination, nucleophilic addition, and transition-metal-catalyzed couplings. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis campaigns and scale-up applications.
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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-H317
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Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: