CAS 3456-79-9

3-Phenyloxindole

Description:

3-Phenyloxindole is an organic compound characterized by its oxindole structure, which features a fused indole and carbonyl group. It is typically represented by a phenyl group attached to the nitrogen of the oxindole moiety. This compound is known for its potential biological activities, including anti-inflammatory and anticancer properties, making it of interest in medicinal chemistry. Its molecular formula generally consists of carbon, hydrogen, and nitrogen atoms, contributing to its aromatic and heterocyclic nature. 3-Phenyloxindole can be synthesized through various chemical reactions, often involving the condensation of appropriate precursors. The compound's solubility can vary depending on the solvent, and it may exhibit different physical properties such as melting point and boiling point based on its purity and crystalline form. Additionally, its reactivity can be influenced by the presence of functional groups, making it a versatile intermediate in organic synthesis. Overall, 3-Phenyloxindole serves as a valuable compound in both research and pharmaceutical applications.

Formula: C₁₄H₁₁NO

InChI: InChI=1S/C14H11NO/c16-14-13(10-6-2-1-3-7-10)11-8-4-5-9-12(11)15-14/h1-9,13H,(H,15,16)

InChI key: InChIKey=PAMMIXSSIGTOAK-UHFFFAOYSA-N

SMILES: O=C1C(C=2C(N1)=CC=CC2)C3=CC=CC=C3

Synonyms:

• 1,3-Dihydro-3-phenyl-2H-indol-2-one
• 2-Indolinone, 3-phenyl-
• 2H-indol-2-one, 1,3-dihydro-3-phenyl-
• 3-Phenyl-1,3-dihydroindol-2-one
• 3-Phenyl-2,3-dihydro-1H-indol-2-one
• 3-Phenyl-2-indolinone
• 3-Phenyloxindole
• NSC 249786
• Oxindole, 3-phenyl-
• 3-Phenyl-1,3-dihydro-2H-indol-2-one