4-Methoxy-2-indolinone, with the CAS number 7699-17-4, is an organic compound characterized by its indolinone structure, which features a fused bicyclic system comprising a benzene ring and a five-membered nitrogen-containing ring. This compound contains a methoxy group (-OCH3) at the 4-position of the indolinone, which influences its chemical reactivity and solubility. Typically, 4-methoxy-2-indolinone exhibits moderate polarity due to the presence of the methoxy group, making it soluble in organic solvents like ethanol and dichloromethane. It is often utilized in organic synthesis and medicinal chemistry, serving as a precursor or intermediate in the development of various pharmaceuticals. The compound may exhibit biological activity, including potential anti-inflammatory or anticancer properties, although specific biological effects can vary based on structural modifications and the presence of other functional groups. As with many organic compounds, proper handling and safety precautions are essential due to potential toxicity or reactivity.

4-Methoxy-2-indolinone

7699-17-4: 4-Methoxy-2-oxindole, 4-Methoxyindolin-2-One, 4-methoxy-1,3-dihydro-2H-indol-2-one

4-Methoxy-2-indolinone is an organic compound that has been optimized for use in palladium catalyzed hydrogenation reactions. The reaction conditions have been determined to be optimized at a temperature of 60°C, with a pressure of 1 bar and a gas hourly space velocity of 100 h-1. The optimum conditions are demonstrated by the result of the bromination reaction, which was completed within 30 minutes. This compound is used as an intermediate in the synthesis of indole compounds and pharmaceuticals.

CAS 7699-17-4: 4-Methoxy-2-indolinone

4-Methoxy-2-indolinone

Ref: 3D-FM31200

4-Methoxyoxindole

Ref: IN-DA003LNT

4-Methoxyoxindole

Ref: 10-F078042

4-Methoxy-2-indolinone

Ref: 54-OR906993