34586-43-1

Usage

Uses

Used in Pharmaceutical Industry:
2-Ethylbenzenesulphonyl chloride is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its reactivity allows for the introduction of the sulphonyl chloride functional group into organic molecules, which is essential for the development of certain drug compounds.
Used in Dye Industry:
In the dye industry, 2-Ethylbenzenesulphonyl chloride is utilized as a chemical intermediate to produce a range of dyes. Its ability to introduce the sulphonyl chloride group into organic molecules contributes to the creation of diverse dye structures with specific properties.
Used in Agrochemical Industry:
2-Ethylbenzenesulphonyl chloride is employed as a chemical intermediate in the production of agrochemicals. Its reactivity plays a crucial role in the synthesis of various agrochemical compounds, such as pesticides and herbicides, which are used to protect crops and enhance agricultural productivity.
Used in Organic Synthesis:
2-Ethylbenzenesulphonyl chloride is used as a reagent in organic synthesis to introduce the sulphonyl chloride functional group into a variety of organic molecules. This allows for the creation of new compounds with specific properties and applications across different industries.

Upstream product

• 95-15-8 Benzo[b]thiophene 
• 1973-22-4 1-bromo-2-ethylbenzene 
• 100-41-4 ethylbenzene 
• 4500-58-7 2-ethylthiophenol 

Downstream Products

• 1119195-38-8 dimethyl (E)-2-(dimethoxyphosphoryl)-3-[(2-ethylphenyl)sulfonyl]-2-butenedioate 
• 1119195-48-0 dimethyl (E)-2-(diethoxyphosphoryl)-3-[(2-ethylphenyl)sulfonyl]-2-butenedioate 
• 1119195-41-3 diethyl (E)-2-(dimethoxyphosphoryl)-3-[(2-ethylphenyl)sulfonyl]-2-butenedioate 
• 1119195-44-6 diethyl (E)-2-(diethoxyphosphoryl)-3-[(2-ethylphenyl)sulfonyl]-2-butenedioate 
• 1351416-37-9 2-ethylbenzenesulfonyl azide 
• 85-92-7 2-Ethylbenzenesulfonamide 
• 84108-98-5 (±)-3-methyl-1,2-benzisothiazoline 1,1-dioxide 
• 131970-58-6 N-[2-(7-Chloro-3,4,5,6-tetrahydro-4-methylfuro[4,3,2-ef]-[3]benzazepin-2-yl)ethyl]benzeneethanesulfonamide 

Relevant academic research and scientific papers

Nitrene transfer catalyzed by a non-heme iron enzyme and enhanced by non-native small-molecule ligands

Transition-metal catalysis is a powerful tool for the construction of chemical bonds. Here we show that Pseudomonas savastanoi ethylene-forming enzyme, a non-heme iron enzyme, can catalyze olefin aziridination and nitrene C-H insertion, and that these activities can be improved by directed evolution. The non-heme iron center allows for facile modification of the primary coordination sphere by addition of metal-coordinating molecules, enabling control over enzyme activity and selectivity using small molecules.

Enantioselective intramolecular benzylic C-H bond amination: Efficient synthesis of optically active benzosultams

'Salen' along: The iridium(III)-salen complex 1 efficiently catalyzes the title reaction of 2-ethylbenzenesulfonyl azides to give five-membered sultams with high enantioselectivity. Other 2-alkyl-substitued substrates lead to five- and six-membered sultam

Endothelin receptor antagonists

Novel compounds of the formula I STR1 in which R 1, R 2, R 3, --A B--C D--, Ar and X have the meaning indicated in claim 1, and their salts show endothelin receptor-antagonistic properties.

CATALYTIC SULFONYLATION OF PHENOL BY STERICALLY HINDERED SULFONYL CHLORIDES

The sulfonylation of phenol by substituted arenesulfonyl chlorides XArSO2Cl in the presence of triethylamine in benzene was studied by potentiometric titration.A linear relation was obtained between the logaritmhs of the catalytic rate constants and the steric constants Eso of the substituents in the sulfonyl chloride.The contribution from the induction and steric effects of the substituents at position2 to the kinetics of the process was assessed.It was concluded that the steric effect plays a predominant role over the induction and resonance effects.