5433-44-3

Usage

Uses

Used in Pharmaceutical Industry:
1,3-di(4-sulfamoylphenyl)triazene is used as a potential antineoplastic and antitumor agent for its ability to release toxic radicals that can target cancer cells. The sulfamoylphenyl groups present in the compound suggest it may have applications similar to those of sulfonamide-containing drugs, which are known for their antibacterial, anti-inflammatory, and antitumor properties.
Further research is necessary to explore the full potential uses and effects of 1,3-di(4-sulfamoylphenyl)triazene, as its specific applications and mechanisms of action in medicinal chemistry are not yet fully understood.

Upstream product

• 63-74-1 sulfanilamide 

Relevant academic research and scientific papers

Electrochemical investigation of some potential antibacterials, II

The electrochemical behaviour of 2-(4'-sulphonamoyl)hydrazonobutyrate- 1,3-diones and sulphonamoylazoaminobenzenes has been studied over a wide range of pH at dropping mercury as well as glassy carbon electrodes. Both types of compounds exhibited a 4c- reduction reaction at both electrodes. At pH > 4.5; 2-(4'-sulphonamoyl)hydrazonobutyrate-1,3-diones exhibited a 2e- reduction wave at higher potentials. Both compounds undergo a 2e- oxidation reaction. On the basis of polarography, linear and cyclic voltammetry, controlled potential electrolysis, coulometry, and spectral analysis, a detailed mechanism has been postulated for the reduction as well as the oxidation. The electrochemical behaviour of 2-(4′-sulphonamoyl)hydrazonobutyrate-1,3-diones and sulphonamoylazoaminobenzenes has been studied over a wide range of pH at dropping mercury as well as glassy carbon electrodes. Both types of compounds exhibited a 4e- reduction reaction at both electrodes. At pH>4.5, 2-(4′-sulphonamoyl)hydrazonobutyrate-1,3-diones exhibited a 2e- reduction wave at higher potentials. Both compounds undergo a 2e- oxidation reaction. On the basis of polarography, linear and cyclic voltammetry, controlled potential electrolysis, coulometry, and spectral analysis, a detailed mechanism has been postulated for the reduction as well as the oxidation.