2578-41-8 Usage
General Description
1H-Imidazole-1-carboxamide, also known as imidazo[4,5-b]pyridin-2-amine, is an organic compound with the molecular formula C5H6N4O. It is a white crystalline powder that is commonly used in the pharmaceutical industry as a building block for the synthesis of various drugs including antifungal and antiparasitic agents. 1H-Imidazole-1-carboxamide has also been studied for its potential use as a corrosion inhibitor in industrial applications due to its ability to form stable complexes with metal ions. Additionally, it has been investigated for its potential as a flame retardant and as a precursor for the synthesis of functional materials. Overall, 1H-Imidazole-1-carboxamide is a versatile chemical with a wide range of potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 2578-41-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,7 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2578-41:
(6*2)+(5*5)+(4*7)+(3*8)+(2*4)+(1*1)=98
98 % 10 = 8
So 2578-41-8 is a valid CAS Registry Number.
2578-41-8Relevant articles and documents
3-(1-Hydroxyalkyl)-1,4,2-dioxazol-5-ones and 3-Hydroxyoxazolidine-2,4-diones from 2-Hydroxycarbohydroxamic Acids and 1,1'-Carbonyldiimidazole
Geffken, Detlef
, p. 211 - 218 (2007/10/02)
The reaction of 2-hydroxycarbohydroxamic acids 6 with 1,1'-carbonyldiimidazole produces 3-(1-hydroxyalkyl)-1,4,2-dioxazol-5-ones 7 and 3-hydroxyoxazolidine-2,4-diones 8.The formation of the heterocycles 7 and 8 depends largely on the substitution at C-2 of 6.Excess of imidazole causes rapid decomposition of 7 into carbonyl compound 9 and isocyanic acid, which yields the adduct 10 with imidazole.Benzylaminolysis of 7a gives 11 whereas the reaction of 7a with 3-chloroaniline produces the ureas 12 and 14 and benzophenone (9a).From the reaction of 7a with imidazole in a mole ratio of 1 : 1 the decomposition products 9a and 10 and 3-hydroxy-5,5-diphenyloxazolidine-2,4-dione (8a) are obtained.