1338062-05-7

Basic information

• Product Name: 4-methyl-N-[(2-propoxyphenyl)-λ³-iodanylidene]benzenesulfonamide
• Synonyms: 4-methyl-N-[(2-propoxyphenyl)-λ³-iodanylidene]benzenesulfonamide
• CAS NO: 1338062-05-7
• Molecular Weight: 431.294
• Mol File: 1338062-05-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-methyl-N-[(2-propoxyphenyl)-λ³-iodanylidene]benzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methyl-N-[(2-propoxyphenyl)-λ³-iodanylidene]benzenesulfonamide(1338062-05-7)
• EPA Substance Registry System: 4-methyl-N-[(2-propoxyphenyl)-λ³-iodanylidene]benzenesulfonamide(1338062-05-7)

Safety Data

• Hazardous Substances Data: 1338062-05-7(Hazardous Substances Data)

Upstream product

• 857825-61-7 1-iodo-2-propoxybenzene 
• 533-58-4 2-Iodophenol 
• 1338061-99-6 (2-propoxyphenyl)-λ³-iodanediyl diacetate 
• 70-55-3 toluene-4-sulfonamide 

Downstream Products

• 57872-24-9 1,1,2,3,4,5-hexahydro-1-<<(4-methylphenyl)sulfonyl>imino>tiophene 1-oxide 
• 24395-14-0 N-(p-tolylsulfonyl)-2-phenylaziridine 
• 13225-54-2 N-(p-toluenesulfonyl)-3-azatricyclo[3.2.1.0^2,4exo] octane 
• 146041-79-4 9-(toluene-4-sulfonyl)-9-aza-bicyclo[6.1.0]nonane 
• 137595-26-7 N-(p-tolylsulfonyl)-1-methyl-7-azabicyclo<4.1.0>heptane 
• 30057-92-2 N-(p-toluenesulfonyl)aminoacetophenone 
• 148961-16-4 2-hexyl-1-(toluene-4-sulfonyl)-aziridine 
• 159659-19-5 1-(4-methylphenylsulfonyl)-2-octylaziridine 
• 69765-78-2 S,S-dibutyl-N-(p-tolylsulfonyl)sulfoximine 
• 147127-08-0 N-(4-tolylsulfonyl)-1,2,3,4-tetrahydronaphthalene-1,2-imine 
• 58107-57-6 4-methyl-N-(2-oxo-cyclohexyl)-benzenesulfonamide 
• 500726-20-5 8-(toluene-4-sulfonyl)-8-azabicyclo[5.1.0]octane 
• 56432-99-6 1-tosylaminoadamantane 
• 42153-74-2 S-methyl-S-phenyl-N-(p-tolylsulfonyl)sulfoximide 

Relevant articles and documents

Development of Imino-λ3-iodanes with Improved Reactivity for Metal-Free [2+2+1] Cycloaddition-Type Reactions

Aiming at the enhancement of electrophilicity of imino-λ3-iodanes, we have developed (tosylimino)pentafluorophenyl-λ3-iodane, which shows superior reactivity compared to the commonly used (tosylimino)phenyl-λ3-iodane in the [2+2+1]-type synthesis of imidazoles. (Figure presented.).

O-alkoxyphenyliminoiodanes: Highly efficient reagents for the catalytic aziridination of alkenes and the metal-free amination of organic substrates

Efficient nitrene precursors: Highly reactive iminoiodane-based nitrene precursors were prepared from ortho-alkoxyiodobenzenes. Owing to the presence of the ortho-substituent on the phenyl ring, these new iminoiodanes have excellent solubility in organic