130552-90-8

Usage

Uses

Used in Pharmaceutical Synthesis:
(E)-N-benzylidenebenzenesulfonamide is used as a building block for the synthesis of various organic compounds and pharmaceuticals. Its unique structure allows it to be a valuable component in the development of new drugs and medications.
Used in Biological Research:
(E)-N-benzylidenebenzenesulfonamide is used as a subject of study for its potential biological activities, such as anti-cancer and anti-inflammatory properties. Researchers are interested in understanding how (E)-N-benzylidenebenzenesulfonamide interacts with biological systems and how it can be utilized for therapeutic purposes.
Used in Coordination Chemistry:
(E)-N-benzylidenebenzenesulfonamide is used in the formation of coordination complexes with various metal ions. This property makes it a useful compound in the field of catalysis and materials science, where it can contribute to the development of new catalysts and materials with specific properties.
Safety Precautions:
It is important to handle (E)-N-benzylidenebenzenesulfonamide with caution, as it can be harmful if ingested or if it comes into contact with the skin or eyes. Proper safety measures should be taken during its use and storage to minimize the risk of exposure.

Upstream product

• 14674-26-1 N-(α-p-Tosyl-benzyl)-benzolsulfonamid 
• 98-10-2 benzenesulfonamide 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 100-52-7 benzaldehyde 
• 70-55-3 toluene-4-sulfonamide 

Downstream Products

• 141-05-9 Diethyl maleate 
• 16340-59-3 1,2-dimethyl-4,5-diphenyl-1H-imidazole 
• 58294-24-9 1,5-Dimethyl-2,4-diphenylimidazole 
• 22397-44-0 1-methyl-2,4,5-triphenyl-1H-imidazole 
• 217947-24-5 N-(1-phenylbut-3-en-1-yl)benzenesulfonamide 
• 837-18-3 N-benzylbenzenesulfonamide 
• 627-27-0 homoalylic alcohol 
• 80735-94-0 1-Phenyl-3-buten-1-ol 
• 25201-44-9 2-methyl-1-phenyl-3-butene-1-ol 

Relevant academic research and scientific papers

Synthesis of 2-chloro-2-imidoylaziridines via aza-darzens-type reaction of 3,3-dichloro-1-azaallylic anions and N-(arylsulfonyl)imines

3,3-Dichloro-1-azaallylic anions, generated by deprotonation of α,α-dichloroketimines 10 with lithium diisopropylamide, reacted with N-sulfonylaldimines 7 to produce the Mannich-type products N-[2,2-dichloro-3- (N-alkylimino)-1,3-diarylpropyl]benzenesulfo

Lewis acid catalyzed dipolar cycloadditions of an activated imidate

An evaluation of simple Lewis acids revealed that N-malonylimidates undergo catalyzed [3+2] cycloaddition reactions with aldehydes, imines, and activated olefins to form oxazolines, imidazolines, and pyrrolines, respectively. Reactions proceed optimally at ambient temperature with the addition of 5 mol % of MgCl2 in CH3CN. Experiments aimed at elucidation of the reactive intermediate undergoing cycloaddition suggest that the Lewis acid promotes a 1,2-prototropic shift to give a metal-coordinated azomethine ylide, rather than ionization and proton transfer to give a nitrile ylide.

An easy synthesis of aliphatic and aromatic N-sulfonyl aldimines

N-Arenesulfonyl aldimines were prepared from aliphatic and aromatic aldehydes in a two-step transformation.

Sulfonimines as bleach catalysts

Novel bleach catalysts, a method for bleaching substrates using these catalysts and detergent compositions containing the catalysts are reported. The catalysts are sulfonimines. Substrates such as fabrics may be bleached in an aqueous solution containing