3413-73-8 Usage
Uses
Used in Pharmaceutical Industry:
(4E)-4-(3-ethyltriazanylidene)-4H-imidazole-5-carboxamide is used as a pharmaceutical intermediate for the development of drugs with antiviral, antibacterial, and antifungal properties. Its unique chemical structure allows it to target specific pathogens and inhibit their growth, making it a valuable asset in the fight against infectious diseases.
Used in Medicinal Chemistry Research:
(4E)-4-(3-ethyltriazanylidene)-4H-imidazole-5-carboxamide is used as a research compound in medicinal chemistry to explore its potential applications and optimize its properties for various therapeutic uses. Its diverse biological activities and unique structure make it an interesting candidate for further investigation and development in the field of drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 3413-73-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,1 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3413-73:
(6*3)+(5*4)+(4*1)+(3*3)+(2*7)+(1*3)=68
68 % 10 = 8
So 3413-73-8 is a valid CAS Registry Number.
3413-73-8Relevant academic research and scientific papers
Antitumour Imidazotetrazines. Part 12. Reactions of Mitozolomide and its 3-Alkyl Congeners with Oxygen, Nitrogen, Halogen, and Carbon Nucleophiles
Baig, Ghouse Unissa,Stevens, Malcolm F. G.
, p. 665 - 670 (2007/10/02)
Mitozolomide (1) and its 3-alkyl congeners ring-open in aqueous sodium carbonate to form 5-(3-alkyltriazen-1-yl)imidazole-4-carboxamides.The 3-methyl and 3-ethyl analogues of mitozolomide decompose in alcohols to form 2-azahypoxanthine and 5-amino-1-alkoxycarbonylimidazole-4-carboxamides.In hydrazine hydrate mitozolomide yields, principally, 5-azidoimidazole-4-carboxamide, whereas the 3-alkyl-derivatives form 5-amino-4-carbamoylimidazole-1-carbohydrazide. 5-Diazoimidazole-4-carboxamide, generated by thermolysis of mitozolomide in acetic acid or pyridine, can be trapped by reactive methylenic ketones, nitriles or esters to afford imidazotriazines.
