1571-93-3 Usage
Uses
Used in Pharmaceutical Research and Development:
2-Methyl-1H-benzoimidazol-5-ylamine hydrochloride is used as a research compound for exploring its potential applications in the pharmaceutical industry. Its diverse biological activities make it a promising candidate for the development of new drugs and therapeutic agents.
Used in Chemical Synthesis:
In the field of organic chemistry, 2-Methyl-1H-benzoimidazol-5-ylamine hydrochloride is used as a synthetic intermediate for the preparation of other complex molecules and compounds. Its unique structure and reactivity contribute to the synthesis of various chemical entities.
Used in Biological Studies:
2-Methyl-1H-benzoimidazol-5-ylamine hydrochloride is employed as a tool compound in biological research to investigate its interactions with biological systems and to understand its potential effects on cellular processes. This can provide insights into its possible therapeutic applications and mechanisms of action.
Check Digit Verification of cas no
The CAS Registry Mumber 1571-93-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,7 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1571-93:
(6*1)+(5*5)+(4*7)+(3*1)+(2*9)+(1*3)=83
83 % 10 = 3
So 1571-93-3 is a valid CAS Registry Number.
1571-93-3Relevant academic research and scientific papers
Hydrogenation on palladium-containing granulated catalysts 3. Synthesis of aminobenzimidazoles by catalytic hydrogenation of dinitroanilines
Elkin,Tolkacheva,Chernysheva,Karmanova,Konyushkin,Semenov
, p. 1216 - 1226 (2008/09/19)
Efficient hydrogenation of o-aminonitrobenzenes on palladium-containing granulated carbon catalysts in carboxylic acid solutions was accompanied by cyclization into aminobenzimidazoles. A simple hydrogenation reactor with a fixed gauze holding a reusable granulated catalyst was designed. Acylated and sulfonylated 4(7)-aminobenzimidazoles were obtained. In terms of electronic and geometrical parameters, they are close analogs of biologically active imidazo[1,5,4-e,f ][1,5]benzodiazepines.
