209251-84-3 Usage
Derivative of phenylamine
2-(4-METHYL-1H-IMIDAZOL-2-YL)-PHENYLAMINE is derived from phenylamine, which is a basic structure in the synthesis of various pharmaceutical compounds.
Imidazole ring attachment
The compound features an imidazole ring attached to the phenyl group, which contributes to its unique chemical properties and potential applications.
Pharmaceutical industry use
It is commonly used as a building block for the synthesis of various drugs and biologically active molecules, making it an important component in the development of new medications.
Medicinal chemistry applications
The compound has potential applications in the field of medicinal chemistry, particularly in the development of new therapeutic agents.
Exhibits different biological activities
2-(4-METHYL-1H-IMIDAZOL-2-YL)-PHENYLAMINE may display various biological activities, which makes it an interesting target for pharmacological research and drug discovery. This versatility allows for the exploration of its potential use in treating a range of medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 209251-84-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,2,5 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 209251-84:
(8*2)+(7*0)+(6*9)+(5*2)+(4*5)+(3*1)+(2*8)+(1*4)=123
123 % 10 = 3
So 209251-84-3 is a valid CAS Registry Number.
209251-84-3Relevant academic research and scientific papers
Imidazo[1,2-c]quinazolines with lipid peroxidation inhibitory effect
Domany, Gyoergy,Gizur, Tibor,Gere, Aniko,Takacs-Novak, Krisztina,Farsang, Gyoergy,Ferenczy, Gyoergy G.,Tarkanyi, Gabor,Demeter, Maria
, p. 181 - 187 (2007/10/03)
A series of imidazo[1,2-c]quinazolines of different lipophilic character was prepared. According to their antioxidant (cyclic voltammetry) properties they all should be potent inhibitors of lipid peroxidation. Under the given circumstances (NADPH-induced lipid peroxidation in rat brain microsomes and Fe2+-induced lipid peroxidation in rat brain homogenate), however, their lipid peroxidation inhibitory activity was strongly dependent on their lipophilicity.
