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Structure of 913240-15-0
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6-Fluoro-1-methylindolin-2-one is a fluorinated indolinone derivative featuring a reactive carbonyl group and a strategically positioned fluorine atom. This scaffold delivers enhanced metabolic stability and modulated electronic properties, making it valuable in medicinal chemistry for constructing bioactive molecules. The methyl substitution improves lipophilicity and binding affinity in target-directed synthesis.
6-Fluoro-1-methylindolin-2-one serves as a versatile building block in medicinal chemistry, enabling efficient access to bioactive indolinone scaffolds. Its fluorinated aryl ring enhances metabolic stability and modulates electronic properties, while the N-methyl amide functionality provides favorable solubility and reactivity in coupling and functionalization reactions. The compound exhibits excellent bench stability and is compatible with standard synthetic transformations, facilitating rapid diversification for drug discovery applications.
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Lot numbers can be found on the outside label of a product: