1620220-67-8

Basic information

• Product Name: 3-({[4-(tert-butyl)phenyl]sulfonyl}methyl)-1,3-dimethyl indolin-2-one
• Synonyms: 3-({[4-(tert-butyl)phenyl]sulfonyl}methyl)-1,3-dimethyl indolin-2-one
• CAS NO: 1620220-67-8
• Molecular Weight: 371.5
• Mol File: 1620220-67-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-({[4-(tert-butyl)phenyl]sulfonyl}methyl)-1,3-dimethyl indolin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-({[4-(tert-butyl)phenyl]sulfonyl}methyl)-1,3-dimethyl indolin-2-one(1620220-67-8)
• EPA Substance Registry System: 3-({[4-(tert-butyl)phenyl]sulfonyl}methyl)-1,3-dimethyl indolin-2-one(1620220-67-8)

Safety Data

• Hazardous Substances Data: 1620220-67-8(Hazardous Substances Data)

Upstream product

• 65604-75-3 4-(tert-butyl)benzenesulfonyl hydrazide 
• 100-61-8 N-methylaniline 
• 15796-89-1 N-methyl-N-phenylmethacrylamide 
• 88576-64-1 4-tert.-Butyl-benzolsulfinsaeure 
• 1611-83-2 2-methyl-N-phenylacrylamide 
• 62-53-3 aniline 
• 15084-51-2 4-tert-butylbenzenesulfonyl chloride 

Relevant articles and documents

Hydrogen and Sulfonyl Radical Generation for the Hydrogenation and Arylsulfonylation of Alkenes Driven by Photochemical Activity of Hydrogen Bond Donor-Acceptor Complexes

An efficient photoinduced strategy for the hydrogenation and arylsulfonylation of alkenes has been developed. The reaction afforded a range of hydrogenated products and sulfonated oxindoles in high yields under external photocatalyst-free, oxidant- and reductant-free conditions. Mechanistic investigations suggested this transformation is driven by the photochemical activity of hydrogen bond donor-acceptor complex, generated from the substrates of arylsulfinic acids and C6-(vinyl sulfone)phenanthridines or N-arylacrylamides via hydrogen bond interaction. (Figure presented.).

Copper-catalyzed arylsulfonylation of N-arylsulfonyl-acrylamides with arylsulfonohydrazides: Synthesis of sulfonated oxindoles

A copper-catalyzed arylsulfonylation of N-arylsulfonyl-acrylamides with sulfonylhydrazides through a tandem radical process was developed. This methodology provided an alternative strategy for the synthesis of sulfonated oxindoles by forming C-S, C-N and C-C bonds in a single operation. the Partner Organisations 2014.