86803-58-9

Basic information

• Product Name: 3-(p-nitrophenyl)-1,4,5,6-tetramethyl-2-thia-3-azabicyclo<2.2.0>hex-5-ene 2,2-dioxide
• Synonyms: 3-(p-nitrophenyl)-1,4,5,6-tetramethyl-2-thia-3-azabicyclo<2.2.0>hex-5-ene 2,2-dioxide
• CAS NO: 86803-58-9
• Molecular Weight: 308.358
• Mol File: 86803-58-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-(p-nitrophenyl)-1,4,5,6-tetramethyl-2-thia-3-azabicyclo<2.2.0>hex-5-ene 2,2-dioxide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(p-nitrophenyl)-1,4,5,6-tetramethyl-2-thia-3-azabicyclo<2.2.0>hex-5-ene 2,2-dioxide(86803-58-9)
• EPA Substance Registry System: 3-(p-nitrophenyl)-1,4,5,6-tetramethyl-2-thia-3-azabicyclo<2.2.0>hex-5-ene 2,2-dioxide(86803-58-9)

Safety Data

• Hazardous Substances Data: 86803-58-9(Hazardous Substances Data)

Upstream product

• 86803-57-8 3-(p-nitrophenyl)-1,4,5,6-tetramethyl-2-thia-3-azabicyclo<2.20>hex-5-ene 2-oxide 
• 13165-67-8 N-sulphinyl-p-nitroaniline 
• 31886-99-4 tetramethylcyclobutadiene*aluminum trichloride 

Relevant articles and documents

Benzvalene and Dewar Benzene Type Sulfinamides

The reaction of cyclobutadiene aluminum halide ? complexes with N-arylsulfinylamines leads, depending on the substitution pattern of the phenyl ring, to either bicyclic (Dewar benzene type) or tricyclic sulfinamides, the latter being formed via an intramolecular Friedel-Crafts reaction of an intermediate cyclobutenyl cation.A similar reaction of aluminum halide ? complex 1 with N-tert-butylsulfinylamine affords both a bicyclic and a tricyclic (benzvalene type) sulfinamide.