5433-44-3 Usage
Description
1,3-di(4-sulfamoylphenyl)triazene is a triazene derivative with the molecular formula C12H14N6O4S2, featuring two sulfamoylphenyl groups. It belongs to a class of compounds known for their antineoplastic, antitumor, and antiviral properties, attributed to their capacity to release toxic radicals in the presence of biological reducing agents. The presence of sulfamoylphenyl groups indicates potential medicinal applications, as sulfonamide-containing compounds have been utilized in the development of drugs with antibacterial, anti-inflammatory, and antitumor properties.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 5433-44-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5433-44:
(6*5)+(5*4)+(4*3)+(3*3)+(2*4)+(1*4)=83
83 % 10 = 3
So 5433-44-3 is a valid CAS Registry Number.
5433-44-3Relevant articles and documents
Electrochemical investigation of some potential antibacterials, II
Jain, Rajeev,Padmaja,Gupta, Seema
, p. 567 - 574 (1997)
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.
