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Structure of 334952-09-9
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2-Oxoindoline-6-carboxylic acid features a fused indoline core with a ketone at the 2-position and a carboxylic acid at the 6-position, providing a rigid, electron-deficient scaffold. This structural motif enables direct incorporation into bioactive molecules, particularly in kinase inhibitor design and medicinal chemistry campaigns requiring polar, planar heterocyclic units. The molecule exhibits bench-stable handling characteristics and compatibility with standard peptide coupling protocols.
2-Oxoindoline-6-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling the construction of indoline-based heterocycles prevalent in kinase inhibitors and CNS-targeted therapeutics. Its orthogonally protected amine and carboxylic acid functionalities facilitate efficient peptide coupling, cyclization, and derivatization under standard synthetic conditions. Bench-stable and amenable to purification via recrystallization or chromatography, it functions reliably in multi-step syntheses requiring functional group tolerance and predictable reactivity.
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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: