6525-97-9

Usage

Chemical family

Quinazolinone

Structural features

Sulfanyl derivative with a 3,4-dichlorophenyl group and a phenyl group attached to a quinazolin-4-one moiety

Potential applications

Pharmaceutical, as a lead compound in drug discovery and development

Need for further studies

Yes, to explore the full potential of this chemical and its derivatives in various drug discovery and development programs.

Upstream product

• 14677-99-7 3-(p-methoxyphenyl)-2-propynenitrile 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 57466-68-9 3-chloro-3-(4-methoxyphenyl)acrylonitrile 
• 14063-79-7 3-chloro-3-(4-methoxyphenyl)acrylaldehyde 
• 768-60-5 4-methoxyphenylacetylen 
• 71707-37-4 2-chloro-3-(4-methoxyphenyl)acrylonitrile 

Relevant academic research and scientific papers

Novel benzenesulfonamide-bearing pyrazoles and 1,2,4-thiadiazoles as selective carbonic anhydrase inhibitors

Two series comprising 20 novel benzenesulfonamides bearing thioureido-linked pyrazole 8 and amino-1,2,4-thiadiazole 10 were synthesized and assayed as human carbonic anhydrase (hCA) inhibitors against isoforms I and II as well as the tumor-associated isof

The study of reactions of α-chlorocinnamonitriles with hydroxylamine

The E-isomers of α-chlorocinnamonitriles react with hydroxylamine to give a mixture of isomeric aminoisoxazoles, while the Z-isomers yield 3-aryl-2-chloroacrylamide oximes.