111105-67-0 Usage
Derivative of imidazole
Imidazole is a heterocyclic aromatic organic compound, which is a building block for this chemical compound.
Contains amino and carbonyl functional groups
These functional groups contribute to the reactivity and potential biological activity of the compound.
Used in organic synthesis and pharmaceutical research
The versatile reactivity of this compound makes it useful in the synthesis of other compounds, and its potential biological activity makes it a valuable research tool.
Ethyl ester group
This group makes the compound easier to handle and transport.
Potential applications in drug development
The biological activity of this compound suggests that it could be used in the development of new drugs and therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 111105-67-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,1,0 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 111105-67:
(8*1)+(7*1)+(6*1)+(5*1)+(4*0)+(3*5)+(2*6)+(1*7)=60
60 % 10 = 0
So 111105-67-0 is a valid CAS Registry Number.
111105-67-0Relevant articles and documents
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.
