97401-95-1

Basic information

• Product Name: Aziridine, 2-(4-bromophenyl)-1-[(4-methylphenyl)sulfonyl]-
• Synonyms: N-(4-tolylsulfonyl)-2-(4-bromophenyl)aziridine;N-(p-tolylsulfonyl)-2-(p-bromophenyl)aziridine;N-(p-toluenesulfonyl)-2-(p-bromophenyl)aziridine;Aziridine,2-(4-bromophenyl)-1-[(4-methylphenyl)sulfonyl];N-(p-tolylsulfonyl)-2-(4-bromophenyl)aziridine;2-(4-bromophenyl)-1-(toluene-4-sulfonyl)aziridine;N-(p-toluenesulfonyl)-2-(4-bromophenyl)aziridine;2-(4-bromophenyl)-1-tosylaziridine
• CAS NO: 97401-95-1
• Molecular Formula: C15H14BrNO2S
• Molecular Weight: 352.252
• Mol File: 97401-95-1.mol
• Article Data: 29

Chemical Properties

• CAS DataBase Reference: Aziridine, 2-(4-bromophenyl)-1-[(4-methylphenyl)sulfonyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Aziridine, 2-(4-bromophenyl)-1-[(4-methylphenyl)sulfonyl]-(97401-95-1)
• EPA Substance Registry System: Aziridine, 2-(4-bromophenyl)-1-[(4-methylphenyl)sulfonyl]-(97401-95-1)

Safety Data

• Hazardous Substances Data: 97401-95-1(Hazardous Substances Data)

Upstream product

• 2039-82-9 1-bromo-4-ethenyl-benzene 
• 55962-05-5 4-methyl-N-[(E)-phenyl-λ³-iodanylidene]benzenesulfonamide 
• 127-65-1 chloroamine-T 
• 98-59-9 p-toluenesulfonyl chloride 
• 1593-60-8 p-toluenesulfonylhydroxylamine 
• 36176-90-6 N-(4-bromobenzylidene)-4-methylbenzenesulfonamide 
• 917-54-4 methyllithium 
• 1122-91-4 4-bromo-benzaldehyde 
• 70-55-3 toluene-4-sulfonamide 
• 6888-79-5 4-bromo-α-methylstyrene 
• 55962-05-5 [N-(p-tolylsulfonyl)imino]phenyliodinane 
• 941-55-9 4-toluenesulfonyl azide 
• 186581-53-3 diazomethane 
• 144-86-5 N-chloro-4-methylbenzenesulfonamide 

Downstream Products

• 1160286-76-9 3-(4-bromophenyl)-5-phenyl-1-tosyl-2,3-dihydro-1H-pyrrole 
• 1188273-72-4 N-(2-(4-bromophenyl)-4-oxo-4-phenylbutyl)-4-methylbenzenesulfonamide 
• 1188273-60-0 3-(4-bromophenyl)-5-(4-methoxyphenyl)-1-tosyl-2,3-dihydro-1H-pyrrole 
• 1188273-74-6 N-(2-(4-bromophenyl)-4-(4-methoxyphenyl)-4-oxobutyl)-4-methylbenzenesulfonamide 
• 1364550-72-0 ethyl (E)-3-(N-(1-(4-bromophenyl)vinyl)-4-methylphenylsulfonamido)acrylate 

Relevant articles and documents

Merging Photoredox/Nickel Catalysis for Cross-Electrophile Coupling of Aziridines with Pyridin-1-ium Salts via Dearomatization

Merging photoredox/nickel catalysis enabling the cross-electrophile coupling of aziridines with pyridin-1-ium salts involving dearomatization for the synthesis of β-(1,4-dihydropyridin-4-yl)-ethylamines, especially including bioactive motif-based analogue

Synthesis of γ-Lactams by Formal Cycloadditions with Ketenes

The synthesis of γ-lactams is reported by a formal (3+2) cycloaddition between readily available ketenes and aziridines or a one-pot formal (2+1+2) cycloaddition using imines as aziridine precursors. The method is practical, is scalable, and affords high yields. It also offers a high level of regio- and diastereoselectivity on a wide range of substrates as well as a high stereoselectivity in the case of enantiopure aziridines.

HKUST-1 Metal Organic Framework as an Efficient Dual-Function Catalyst: Aziridination and One-Pot Ring-Opening Transformation for Formation of β-Aryl Sulfonamides with C-C, C-N, C-S, and C-O Bonds

Metal-organic frameworks (MOFs) are extensively used in catalysis due to their robust structure, well-defined periodic reaction centers, and high porosity. We report Cu3(BTC)2·(H2O)3 (HKUST-1) as an efficient heterogeneous catalyst for aziridination of al