17260-67-2

Usage

Uses

Used in Pharmaceutical Industry:
2-Chloro-N-methylbenzenesulphonamide is used as an antimicrobial agent for its ability to inhibit the growth of bacteria, making it a valuable component in the development of pharmaceuticals aimed at treating bacterial infections.
Used in Manufacturing of Dyes:
In the dye industry, 2-Chloro-N-methylbenzenesulphonamide is utilized in the production of dyes, contributing to the coloration and stability of various products.
Used as a Preservative:
2-Chloro-N-methylbenzenesulphonamide is used as a preservative in different products to prevent microbial contamination and extend the shelf life of the products.
Used in Chemical Synthesis:
2-Chloro-N-methylbenzenesulphonamide serves as a solubilizing agent in the synthesis of other chemicals, facilitating the process and improving the efficiency of chemical reactions.

InChI:InChI=1/C7H8ClNO2S/c1-9-12(10,11)7-5-3-2-4-6(7)8/h2-5,9H,1H3

Upstream product

• 74-89-5 methylamine 
• 2905-23-9 2-chlorophenylsulfonyl chloride 
• 67-56-1 methanol 
• 6961-82-6 2-chlorobenzenesulfonamide 

Relevant academic research and scientific papers

Recyclable covalent triazine framework-supported iridium catalyst for the N-methylation of amines with methanol in the presence of carbonate

An iridium complex Cp*Ir@CTF, which is synthesized by the coordinative immobilization of [Cp*IrCl2]2 on a functionalized covalent triazine framework (CTF), was found to be a general and highly efficient catalyst for the N-methylation of amines with methanol in the presence of carbonate. Under environmentally benign conditions, a variety of desirable products were obtained in high yields with complete selectivities and functional group friendliness. Furthermore, the synthesized catalyst could be recycled by simple filtration without obvious loss of catalytic activity after sixth cycle. Notably, this research exhibited the potential of covalent triazine framework-supported transition metal catalysts for hydrogen autotransfer process.

Method for synthesizing N-methyl sulfonamide in water

The invention discloses a method N - for synthesizing,methylsulfamide in water, by using a transition metal iridium catalyst to catalyze N - methylation reaction. by using a non-toxic and harmless water as a solvent, to avoid using the organic agent; to react only as a byproduct, without an environmental hazard; reaction temperature with respect to the previous strip more mild; and have a wide application prospect; with high selectivity, reaction atomic economy.

N-Methylation of Amines with Methanol in Aqueous Solution Catalyzed by a Water-Soluble Metal-Ligand Bifunctional Dinuclear Iridium Catalyst

The N-methylation of amines with methanol in aqueous solution was proposed and accomplished by using a water-soluble metal-ligand bifunctional dinuclear iridium catalyst. In the presence of [(Cp*IrCl)2(thbpym)][Cl]2 (1 mol %), a range of desirable products were obtained in high yields under environmentally benign conditions. Notably, this research exhibited the potential of transition metal-catalyzed activation of methanol as a C1 source for the construction of the C-N bond in aqueous solution.

Novel arylsulphonamide derivatives and use thereof as therapeutic agents

The present invention relates to novel arylsulphonamide compounds, defined by formula I and the description, as well as their method of preparation and their therapeutic use.

TACHYKININ RECEPTOR ANTAGONISTS

The present invention relates to selective NK-1 receptor antagonists of Formula (I) or a pharmaceutically acceptable salt thereof, for the treatment of disorders associated with an excess of tachykinins.