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Structure of 4192-28-3
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(S)-2-(1,3-Dioxoisoindolin-2-yl)propanoic acid features a chiral α-carbon adjacent to a reactive isoindolinone scaffold, enabling selective functionalization in asymmetric synthesis. The fused bicyclic core delivers high structural rigidity and electron-deficient character, enhancing its utility in conjugate addition reactions and as a building block for bioactive heterocycles under standard bench conditions.
(S)-2-(1,3-Dioxoisoindolin-2-yl)propanoic acid serves as a versatile building block in medicinal chemistry, enabling efficient access to isoindoline-based scaffolds prevalent in bioactive molecules. Its chiral α-amino acid structure facilitates stereoselective transformations and offers robust functional group tolerance, supporting downstream derivatization via amide coupling, reduction, or cyclization. The molecule exhibits excellent bench stability and ease of purification, making it well-suited for scalable synthesis and high-throughput screening campaigns.
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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: