1415726-82-7

Basic information

• Product Name: (S)-3-benzyl-3-(2-(4-bromophenyl)-2-oxoethyl)indolin-2-one
• Synonyms: (S)-3-benzyl-3-(2-(4-bromophenyl)-2-oxoethyl)indolin-2-one
• CAS NO: 1415726-82-7
• Molecular Weight: 420.305
• Mol File: 1415726-82-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-3-benzyl-3-(2-(4-bromophenyl)-2-oxoethyl)indolin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-3-benzyl-3-(2-(4-bromophenyl)-2-oxoethyl)indolin-2-one(1415726-82-7)
• EPA Substance Registry System: (S)-3-benzyl-3-(2-(4-bromophenyl)-2-oxoethyl)indolin-2-one(1415726-82-7)

Safety Data

• Hazardous Substances Data: 1415726-82-7(Hazardous Substances Data)

Upstream product

• 1398681-59-8 3-benzyl-3-bromoindolin-2-one 
• 64929-35-7 3-(4-bromophenyl)-3-oxopropanoic acid 

Relevant articles and documents

Organocatalyzed enantioselective decarboxylative stereoablation reaction for the construction of 3,3′-disubstituted oxindoles using β-ketoacids and 3-halooxindoles

An unprecedented method for the construction of optically active 3,3′-disubstituted oxindoles via an organocatalyzed decarboxylative stereoablation reaction has been developed. We describe the first asymmetric reaction between β-ketoacids and 3-halooxindoles utilizing an organocatalyst. This method allows for the formation of a variety of 3,3′-disubstituted oxindoles bearing a keto-carbonyl group, which are not easily accessible using other methodologies, in moderate to good yields with high enantioselectivities.