5428-22-8 Usage
Uses
Used in Pharmaceutical Research:
1-(2,2-diphenylethyl)-4-(2-fluorophenyl)piperazine is used as a potential therapeutic agent for various psychiatric conditions due to its action as a serotonin and dopamine receptor antagonist. Its application aims to address conditions such as anxiety, depression, and schizophrenia, providing new avenues for treatment and management of these disorders.
Used in Neuropharmacology:
In the field of neuropharmacology, 1-(2,2-diphenylethyl)-4-(2-fluorophenyl)piperazine is utilized for its potential to contribute to the understanding of serotonin and dopamine receptor interactions. Its unique structure and pharmacological properties make it a valuable tool for further research and development, potentially leading to the creation of novel drugs targeting the central nervous system.
Used in Addiction Treatment Research:
1-(2,2-diphenylethyl)-4-(2-fluorophenyl)piperazine is also being studied for its potential use in the treatment of drug addiction and substance abuse disorders. As a compound with receptor antagonist properties, it may offer new insights and therapeutic approaches to combat addiction, aiding in the development of more effective treatment strategies.
Overall, 1-(2,2-diphenylethyl)-4-(2-fluorophenyl)piperazine's diverse applications in pharmaceutical research, neuropharmacology, and addiction treatment research highlight its potential as a versatile compound with significant implications for future drug development and therapeutic interventions.
Check Digit Verification of cas no
The CAS Registry Mumber 5428-22-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,2 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5428-22:
(6*5)+(5*4)+(4*2)+(3*8)+(2*2)+(1*2)=88
88 % 10 = 8
So 5428-22-8 is a valid CAS Registry Number.
5428-22-8Relevant academic research and scientific papers
Antimalarials. 10. Substituted 3 halo and 3 methoxy 2 aryl 4 quinoline (di n butylaminomethyl) methanols
Munson Jr.,Johnson,Sanders,Ohnmacht,Lutz
, p. 1232 - 1236 (2007/10/08)
Four 2 aryl 4 quinoline (di n butyl amino methyl) methanols with Br, Cl, F, or OMe in position 3 were synthesized by modifications of standard reactions. The antimalarial activity decreased with increased size of the 3 substituent. The 3 F 4',6,8 Cl3
