64096-91-9 Usage
Uses
Used in Medicinal Chemistry:
4H-Pyrazolo[1,5-a]benzimidazole-3-carbonitrile(9CI) is used as a chemical scaffold for the development of new pharmaceutical agents due to its distinctive molecular architecture and the presence of the nitrile group, which can be further modified to enhance its biological activity.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4H-Pyrazolo[1,5-a]benzimidazole-3-carbonitrile(9CI) is utilized as a starting material or intermediate in the synthesis of various drug candidates. Its heterocyclic nature and the nitrile group provide opportunities for chemical modifications that can lead to the discovery of novel therapeutic agents with improved efficacy and selectivity.
Further studies are required to fully explore the properties and potential uses of 4H-Pyrazolo[1,5-a]benzimidazole-3-carbonitrile(9CI), as its current applications are based on its structural features and the possibilities they present in the realm of medicinal chemistry and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 64096-91-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,9 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 64096-91:
(7*6)+(6*4)+(5*0)+(4*9)+(3*6)+(2*9)+(1*1)=139
139 % 10 = 9
So 64096-91-9 is a valid CAS Registry Number.
64096-91-9Relevant academic research and scientific papers
Khan, Misbahul A.,Ribeiro, Vera L. T.
, p. 425 - 432 (1983)
The 4H-Pyrazolobenzimidazole ring system was prepared by an intramolecular Ullmann arylation of 4-substituted 1-(o-aminophenyl)pyrazole while other derivatives were obtained by functional group modifications.Some electrophilic substitutions (nitration, bromination) and alkylations were also carried out. - Keywords: Alkylation; Bromination; Nitration; Ullmann arylation
