1130682-56-2

Basic information

• Product Name: 1-(2-benzenesulfonylethyl)-3-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecylsulfanyl)-5-methyl-3-(2-nitrobenzyl)-1,3-dihydroindol-2-one
• Synonyms: 1-(2-benzenesulfonylethyl)-3-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecylsulfanyl)-5-methyl-3-(2-nitrobenzyl)-1,3-dihydroindol-2-one
• CAS NO: 1130682-56-2
• Molecular Weight: 928.688
• Mol File: 1130682-56-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(2-benzenesulfonylethyl)-3-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecylsulfanyl)-5-methyl-3-(2-nitrobenzyl)-1,3-dihydroindol-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-benzenesulfonylethyl)-3-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecylsulfanyl)-5-methyl-3-(2-nitrobenzyl)-1,3-dihydroindol-2-one(1130682-56-2)
• EPA Substance Registry System: 1-(2-benzenesulfonylethyl)-3-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecylsulfanyl)-5-methyl-3-(2-nitrobenzyl)-1,3-dihydroindol-2-one(1130682-56-2)

Safety Data

• Hazardous Substances Data: 1130682-56-2(Hazardous Substances Data)

Upstream product

• 1130682-52-8 1-(2-benzenesulfonylethyl)-3-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecylsulfanyl)-5-methyl-1,3-dihydroindol-2-one 
• 577-19-5 2-nitrophenyl bromide 

Relevant articles and documents

Formation of N-heterocycles by the reaction of thiols with glyoxamides: Exploring a connective Pummerer-type cyclisation

The reaction of thiols with glyoxamides provides a convenient method for the generation of thionium ions and the initiation of Pummerer-type reactions. When the glyoxamides contain tethered aromatic nucleophiles, N-heterocycles are formed by a thionium ion cyclisation. The scope and mechanism of the connective Pummerer-type process has been investigated using a range of thiols, Lewis acids and both mono- and bis-glyoxamides. The utility of the process has been illustrated in a synthesis of the indoloquinoline natural product, neocryptolepine. The Royal Society of Chemistry 2009.