5-Bromo-3-ethyl-2-oxindole is a chemical compound characterized by its oxindole structure, which features a bicyclic framework consisting of a benzene ring fused to a pyrrolidine ring. The presence of a bromine atom at the 5-position and an ethyl group at the 3-position contributes to its unique reactivity and properties. This compound typically exhibits moderate solubility in organic solvents, and its molecular structure may influence its biological activity, making it of interest in medicinal chemistry. The bromine substituent can enhance electrophilic reactivity, while the ethyl group may affect steric hindrance and lipophilicity. 5-Bromo-3-ethyl-2-oxindole may also participate in various chemical reactions, including nucleophilic substitutions and cycloadditions, which are valuable in synthetic organic chemistry. Its potential applications could extend to pharmaceuticals, where derivatives of oxindole compounds are often explored for their therapeutic properties. As with many chemical substances, safety data and handling precautions should be considered when working with this compound.

5-Bromo-3-ethyl-2-oxindole

304876-05-9: 5-Bromo-3-ethyl-1,3-dihydroindol-2-one, 5-bromo-3-ethyl-1,3-dihydro-2H-indol-2-one

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CAS 304876-05-9: 5-Bromo-3-ethyl-2-oxindole

5-Bromo-3-ethyl-2-oxindole

Ref: 3D-FB146997

2H-Indol-2-one, 5-bromo-3-ethyl-1,3-dihydro-

Ref: IN-DA0030BN

5-bromo-3-ethyl-2,3-dihydro-1H-indol-2-one

Ref: 10-F526218

5-Bromo-3-ethyl-2-oxindole

Ref: 54-OR01753