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Structure of 32999-55-6
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This amino acid derivative features a fused indolinone scaffold with a strategically positioned amino and carboxylate group, enabling direct integration into peptide-based systems. The electron-deficient indolinone ring enhances stability and modulates reactivity in synthetic workflows. Ideal for bioconjugation and medicinal chemistry applications requiring rigid, polar scaffolds.
2-Amino-3-(2-oxoindolin-3-yl)propanoic acid serves as a key building block for indoline-based scaffolds in medicinal chemistry. Its functional groups—amine, carboxylic acid, and ketone—enable diverse transformations including amidation, esterification, and reductive amination. The molecule exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis 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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: