52601-81-7

Usage

Uses

Used in Pharmaceutical Industry:
[(4-methylphenyl)sulfonyl]iminodiethane-2,1-diyl dimethanesulfonate is used as a potential inhibitor for the treatment of diseases. Its sulfonamide structure and sulfonyl group contribute to its potential effectiveness in targeting specific biological pathways, making it a valuable compound for drug development and therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, [(4-methylphenyl)sulfonyl]iminodiethane-2,1-diyl dimethanesulfonate is used as a component in the development of pesticides and other agricultural chemicals. Its sulfonyl group provides a foundation for creating compounds that can target and control pests, weeds, and diseases affecting crops, thereby enhancing agricultural productivity and crop protection.
Used in Chemical Processes:
[(4-methylphenyl)sulfonyl]iminodiethane-2,1-diyl dimethanesulfonate also finds application in various chemical processes due to its unique chemical structure. It can be utilized as an intermediate or reactant in the synthesis of other complex molecules, contributing to the advancement of chemical research and the development of novel materials and products.

Upstream product

• 7146-67-0 N-tosyldiethanolamine 
• 124-63-0 methanesulfonyl chloride 

Downstream Products

• 344236-45-9 N,N-Bis-(3-isocyanato-3-methyl-butyl)-4-methyl-benzenesulfonamide 
• 74568-87-9 4,4'-<<(4-Methylphenyl)sulfonyl>imino>bis<2,2-dimethylbutansaeure> 
• 74568-89-1 4,4'-<<(4-Methylphenyl)sulfonyl>imino>bis<2,2-dimethylbutansaeurechlorid> 
• 74568-91-5 4,4'-<<(4-Methylphenyl)sulfonyl>imino>bis<2,2-dimethylbutansaeureazid> 
• 343858-72-0 N,N-Bis-(3-allyl-3-isocyanato-hex-5-enyl)-4-methyl-benzenesulfonamide 
• 74568-86-8 4,4'-<<(4-Methylphenyl)sulfonyl>imino>bis<2,2-diallylbutansaeure> 
• 74568-88-0 4,4'-<<(4-Methylphenyl)sulfonyl>imino>bis<2,2-diallylbutansaeurechlorid> 
• 74568-93-7 N,N-Bis(3-amino-3,3-dimethylpropyl)-4-methylbenzolsulfonamid Dihydrochlorid 
• 74568-90-4 4,4'-<<(4-Methylphenyl)sulfonyl>imino>bis<2,2-diallylbutansaeureazid> 
• 74568-92-6 N,N-bis(3-amino-3,3-diallylpropyl)-4-methylbenzosulfonamide dihydrochloride 
• 112193-80-3 1-benzyl-4,7,10-tris(p-toluenesulfonyl)-1,4,7,10-tetraazacyclododecane 
• 52667-88-6 cyclen tetratosylate 
• 374805-44-4 10-(p-tolylsulfonyl)-1,4,7-trithia-10-azacyclododecane 
• 870064-57-6 3-methyl-5-(4-tosyl-piperazin-1-yl)-1,2,3,4-tetrahydroquinoline 

Relevant academic research and scientific papers

Chromogenic and fluorogenic crown ether compounds for the selective extraction and determination of Hg(II)

Two novel crown ether compounds, N,N′-bis(2-hydroxy-5-nitrobenzyl)-4,13-diazadibenzo-18-crown-6 (CCE) and N,N′-bis(7-hydroxy-4-methylcoumarin-8-methylene)-4,13-diazadibenzo-18- crown-6 (FCE), have been synthesized as potential reagents for the selective e

Enantiomers of 1-[(4-chlorophenyl)phenylmethyl]-4-[(4-methylphenyl) sulfonyl]piperazine

Levorotatory and dextrorotatory enantiomers of 1-[(4-chlorophenyl)phenylmethyl]-4-[(4-methylphenyl)sulfonyl]piperazine of the formula STR1 their preparation and use for the preparation of substantially optically pure enantiomers of 1-[(4-chlorophenyl)phenylmethyl]piperazine, which are themselves valuable intermediate products for the preparation of optically active therapeutic compounds having a very high degree of optical purity.

Chromogenic Diaza-Crown Ether Dicarboxylic Acids for Determination of Calcium Ions

The synthesis of two novel calcium chromoionophores 2 and 3, which are based on a benzodiazacrown ether with an inward-facing methoxyl group and bear two acetic acid groups and a 2,4,6-trinitroanilino chromophore, is described.Calcium and magnesium respon

Synthesis of Symmetrically Substituted Bicyclic Guanidines

The symmetrically 2,2,8,8-tetraalkylsubstituted bicyclic guanidines 14a and b are prepared stereoselectively via construction of the open-chain triamines 11a and b and subsequent cyclisation.A one-pot reaction gives the unsubstituted guanidine 14c in high