Fluorophenibut
- Molecular formula
- C27H27ClF2N4O
- CAS Number
- 262868-44-8
- IUPAC Name
- 3-[1-[4-(2-chloro-4-fluoro-phenyl)-4-(4-fluorophenyl)butyl]-4-piperidyl]-1H-benzimidazol-2-one
- Molecular Weight
- 482.92g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2560g/cm3
- Synonyms
- Bio1_001140
Identification
Interesting Facts about 3-[1-[4-(2-chloro-4-fluoro-phenyl)-4-(4-fluorophenyl)butyl]-4-piperidyl]-1H-benzimidazol-2-one
This compound belongs to a class of chemical compounds known as benzimidazoles, which are characterized by a fused benzene and imidazole ring. They demonstrate a wide array of biological activities, making them a significant subject of research in pharmacology.
Key Characteristics:
- Pharmaceutical Applications: Benzimidazole derivatives often exhibit potent inhibitory actions against various targets in biological systems. This specific compound, for instance, has been studied for its potential in treating disorders related to the central nervous system.
- Fluorinated Phenyl Groups: The presence of fluorine atoms in its structure enhances the electronic properties of the compound, potentially influencing its binding affinity and selectivity to specific biological targets.
- Chlorine Substitution: The incorporation of chlorine introduces steric effects, which can significantly modulate the pharmacokinetics of the compound, making it both a subject of interest for medicinal chemistry and a fascinating example of halogenated molecule design.
Interestingly, the design of such compounds often reflects the balance between potency, selectivity, and toxicity. As quoted in one of the leading articles, “The ideal drug should be one that is effective at low doses and has minimal side effects.” Compounds like this one represent the ongoing quest for optimal therapeutics in modern medicine.
In addition to their medicinal implications, the chemical synthesis of such complex organic compounds challenges chemists to develop innovative synthetic pathways, showcasing the brilliance of chemical synthesis and the intricate web of organic reactivity.
Overall, 3-[1-[4-(2-chloro-4-fluoro-phenyl)-4-(4-fluorophenyl)butyl]-4-piperidyl]-1H-benzimidazol-2-one serves as an exemplary model for exploring the intersection of chemical ingenuity and therapeutic potential.