200803-17-4

Basic information

• Product Name: Aziridine, 2-(2-bromophenyl)-1-[(4-methylphenyl)sulfonyl]-
• CAS NO: 200803-17-4
• Molecular Formula: C15H14BrNO2S
• Molecular Weight: 352.252
• Mol File: 200803-17-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Aziridine, 2-(2-bromophenyl)-1-[(4-methylphenyl)sulfonyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Aziridine, 2-(2-bromophenyl)-1-[(4-methylphenyl)sulfonyl]-(200803-17-4)
• EPA Substance Registry System: Aziridine, 2-(2-bromophenyl)-1-[(4-methylphenyl)sulfonyl]-(200803-17-4)

Safety Data

• Hazardous Substances Data: 200803-17-4(Hazardous Substances Data)

Upstream product

• 2039-88-5 2-bromostyrene 
• 55962-05-5 4-methyl-N-[(E)-phenyl-λ³-iodanylidene]benzenesulfonamide 
• 127-65-1 chloroamine-T 
• 55962-05-5 [N-(p-tolylsulfonyl)imino]phenyliodinane 
• 70-55-3 toluene-4-sulfonamide 

Downstream Products

• 31271-90-6 1-(p-toluenesulfonyl)-1H-indole 
• 1429656-32-5 3-(2,3-dimethylphenoxy)-1-tosylindoline 
• 1429656-22-3 N-(2-(2-bromophenyl)-2-(2,3-dimethylphenoxy)ethyl)-4-methylbenzenesulfonamide 
• 1429656-31-4 3-(p-tolyloxy)-1-tosylindoline 
• 1429656-21-2 N-(2-(2-bromophenyl)-2-(p-tolyloxy)ethyl)-4-methylbenzenesulfonamide 
• 1429656-30-3 3-(m-tolyloxy)-1-tosylindoline 
• 1429656-20-1 N-(2-(2-bromophenyl)-2-(m-tolyloxy)ethyl)-4-methylbenzenesulfonamide 
• 1429656-29-0 3-(4-tert-butylphenoxy)-1-tosylindoline 
• 1429656-19-8 N-(2-(2-bromophenyl)-2-(4-tert-butylphenoxy)ethyl)-4-methylbenzenesulfonamide 
• 1429656-28-9 3-(o-tolyloxy)-1-tosylindoline 

Relevant articles and documents

Transition-Metal-Free Stereospecific Oxidative Annulative Coupling of Indolines with Aziridines

Tandem C-N bond formation for the oxidative annulation of indolines with aziridines is accomplished employing the combination of DDQ and NaOCl at ambient conditions. Optically active aziridine can be coupled with high enantiomeric purity (>99% ee). The substrate scope, stereocontrol with the enantioenriched substrate, and scale-up are the important practical advantages.

Copper iodide-catalyzed aziridination of alkenes with sulfonamides and sulfamate esters

An efficient copper iodide-catalyzed aziridination of a variety of alkenes with sulfonamides and sulfamate esters as the nitrogen source and iodosylbenzene (PhI{double bond, long}O) as the oxidant is reported herein. The reaction is operationally straight

Efficient Aziridination of Olefins Catalyzed by a Unique Disilver(I) Compound

A unique disilver(I) compound is an efficient catalyst for aziridination of olefins. Copyright