5282-81-5

Usage

Chemical classification

sulfonamide compound

Purpose

used in the production of drugs and pharmaceuticals

Known for

antibacterial and diuretic properties

Contains

a. Naphthalenesulfonamide group
b. Dimethylamino group
c. Phenylethyl group

Potential use

synthesis of various medicinal products

Safety precaution

handle with caution and according to safety guidelines

Upstream product

• 605-65-2 5-(dimethylamino)naphth-1-ylsulfonyl chloride 
• 64-04-0 phenethylamine 
• 126402-46-8 4-(4,8-Dimethoxy-naphthalen-1-ylmethyl)-N-phenethyl-benzenesulfonamide 

Relevant academic research and scientific papers

LIBRARIES OF N-SUBSTITUTED-N-PHENYLETHYLSULFONAMIDES FOR DRUG DISCOVERY

New compounds are continually being sought for the treatment and prevention of disorders. The invention relates to N-substituted-N-phenylethylsulfonamides libraries which can be used in the search for, and identification of, new lead compounds that could

N-SUBSTITUTED-N-PHENYLETHYLSULFONAMIDES FOR THE IDENTIFICATION OF BIOLOGICAL AND PHARMACOLOGICAL ACTIVITY

Novel compounds are continually sought after to treat and prevent diseases and disorders. The invention relates to N-substituted-N-phenylethylsulfonamides useful for being biologically and pharmacologically screened, and to contribute to the exploration and identification of new lead molecules that are capable of modulating the functional activity of a biological target.

N-SUBSTITUTED-N-PHENYLETHYLSULFONAMIDES FOR THE IDENTIFICATION OF BIOLOGICAL AND PHARMACOLOGICAL ACTIVITY

Novel compounds are continually sought after to treat and prevent diseases and disorders. The invention relates to N-substituted-N-phenylethylsulfonamides of formula (I) useful for being biologically and pharmacologically screened, and to contribute to th

A NEW AMINO PROTECTING GROUP READILY REMOVABLE WITH NEAR ULTRAVIOLET LIGHT AS AN APPLICATION OF ELECTRON-TRANSFER PHOTOCHEMISTRY

As an extension of organic photochemistry via intermolecular electron-transfer in donor-acceptor pair systems between electron-rich aromatic compounds and electron-deficient tosyl groups, we report here a new protecting group for the amino-function, 4-(4,8-dimethoxy-naphthylmethyl)benzenesulfonyl (DNMBS) group, which is readily removed, via an intramolecular electron-transfer followed by hydrolysis, with a high quantum efficiency on irradiation with light longer than 300 nm.