141939-07-3

Basic information

• Product Name: 2H-Indol-2-one, 1-acetyl-1,3-dihydro-3-hydroxy-3-(2-oxo-2-phenylethyl)-
• CAS NO: 141939-07-3
• Molecular Formula: C18H15NO4
• Molecular Weight: 309.321
• Mol File: 141939-07-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2H-Indol-2-one, 1-acetyl-1,3-dihydro-3-hydroxy-3-(2-oxo-2-phenylethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-Indol-2-one, 1-acetyl-1,3-dihydro-3-hydroxy-3-(2-oxo-2-phenylethyl)-(141939-07-3)
• EPA Substance Registry System: 2H-Indol-2-one, 1-acetyl-1,3-dihydro-3-hydroxy-3-(2-oxo-2-phenylethyl)-(141939-07-3)

Safety Data

• Hazardous Substances Data: 141939-07-3(Hazardous Substances Data)

Upstream product

• 574-17-4 1-acetyl-1H-indole-2,3-dione 
• 614-20-0 3-oxo-3-phenylpropionic acid 
• 21905-78-2 N-acetyloxindole 
• 70-11-1 α-bromoacetophenone 
• 532-27-4 1-chloroacetophenone 
• 7257-94-5 1-phenyl-2-(p-tolylsulfonyloxy)ethanone 

Downstream Products

• 88730-73-8 3-Hydroxy-3-(2-oxo-2-phenyl-ethyl)-1,3-dihydro-indol-2-one 

Relevant articles and documents

An unprecedented protocol for the synthesis of 3-hydroxy-3-phenacyloxindole derivatives with indolin-2-ones and α-substituted ketones

An unprecedented reaction between indolin-2-ones and α-substituted ketones has been developed. Using this protocol, a wide range of biologically important 3-hydroxy-3-phenacyloxindole derivatives could be obtained in good yield (up to 93%) under mild reaction conditions. A possible mechanism of this reaction was tentatively proposed based on some control experiments and MS spectrometry analysis.