155721-36-1

Basic information

• Product Name: Aziridine, 2-(4-methoxyphenyl)-1-[(4-methylphenyl)sulfonyl]-
• CAS NO: 155721-36-1
• Molecular Formula: C16H17NO3S
• Molecular Weight: 303.382
• Mol File: 155721-36-1.mol
• Article Data: 28

Chemical Properties

• CAS DataBase Reference: Aziridine, 2-(4-methoxyphenyl)-1-[(4-methylphenyl)sulfonyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Aziridine, 2-(4-methoxyphenyl)-1-[(4-methylphenyl)sulfonyl]-(155721-36-1)
• EPA Substance Registry System: Aziridine, 2-(4-methoxyphenyl)-1-[(4-methylphenyl)sulfonyl]-(155721-36-1)

Safety Data

• Hazardous Substances Data: 155721-36-1(Hazardous Substances Data)

Upstream product

• 637-69-4 4-Methoxystyrene 
• 127-65-1 chloroamine-T 
• 593-71-5 Chloroiodomethane 
• 14674-38-5 (E)-N-(4-methoxybenzylidene)-4-methylbenzenesulfonamide 
• 70-55-3 toluene-4-sulfonamide 
• 55962-05-5 [N-(p-tolylsulfonyl)imino]phenyliodinane 
• 1058-14-6 N-p-tolylsulfonylphosphine imide 

Downstream Products

• 182323-20-2 N-(2-(4-methoxyphenyl)-2-oxoethyl)-4-methylbenzenesulfonamide 
• 1071204-68-6 C₂₄H₂₄N₂O₃S 
• 1071204-69-7 2-ethyl-4,5-dihydro-4-(4-methoxyphenyl)-1-p-tosyl-1H-imidazole 
• 1374294-68-4 2-(4-methoxyphenyl)-7-methyl-4-tosyl-1,2,3,4-tetrahydro-5H-1,4-benzodiazepin-5-one 

Relevant articles and documents

Manganese-catalyzed aziridination of olefins with chloramine-T in water and buffered aqueous solutions

A water-soluble, manganese-porphyrin complex was used to catalytically generate aziridines from olefins in moderate to good yields (up to 93%) upon optimization at room temperature and in aqueous media. Reactions using chloramine-T at slightly acidic to n

Make It Green: Copper-Catalyzed Olefin Aziridination in Water with an Iminoiodonane

The copper complex Tp(CF3)2,BrCu(NCMe) efficiently catalyses the aziridination of olefins in water using PhI=NTs as the nitrene source, with identical activity than that observed when using dichloromethane as the solvent, under the same experim

Catalytic Asymmetric [3 + 2] Annulation of Hantzsch Esters with Racemic N-Sulfonylaziridines

Hantzsch esters (HEs) served as two-carbon partners in a copper(I)-catalyzed enantioselective [3 + 2] annulation with racemic 2-(hetero)aryl-N-sulfonyl aziridines via kinetic resolution to provide pyrrolo[2,3-b]tetrahydropyridines containing multiple contiguous stereogenic centers including all-carbon quaternary centers in excellent yields and enantiopurities and moderate-to-excellent diastereoselectivities. Mainly dependent upon the structures of the aziridines, a competitive hydrogenolysis process with HEs as the hydrogen source was also observed in some cases.