Fluorobutyrylfentanyl Chloride
- Molecular formula
- C19H23ClFNO
- CAS Number
- 1185887-21-1
- IUPAC Name
- 4-(3a,4,7,7a-tetrahydro-1H-isoindol-2-ium-2-yl)-1-(4-fluorophenyl)butan-1-one;chloride
- Molecular Weight
- 371.87g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2500g/cm3
Identification
Interesting Facts about 4-(3a,4,7,7a-Tetrahydro-1H-Isoindol-2-Ium-2-Yl)-1-(4-Fluorophenyl)Butan-1-One;Chloride
The compound 4-(3a,4,7,7a-tetrahydro-1H-isoindol-2-ium-2-yl)-1-(4-fluorophenyl)butan-1-one; chloride is a fascinating molecule that draws interest from various branches of chemistry, particularly medicinal chemistry and pharmacology. Here are some compelling aspects of this compound:
- Structural Complexity: The presence of the isoindolin substructure gives this compound unique properties, characterized by a fused ring system. This structure can contribute to various biological activities and interactions.
- Fluorine Substitution: The inclusion of a fluorine atom in the para position of the phenyl group significantly enhances the molecular stability and lipophilicity of the compound, potentially increasing its bioavailability.
- Psychoactive Potential: Compounds featuring the isoindoline moiety have been noted for their diverse pharmacological profiles. They are often studied for various neurological effects and may impact neurotransmitter systems.
- Electrophilic Interactions: The positively charged nitrogen center in the isoindolium structure allows for interesting interactions with nucleophiles, making it a versatile candidate for chemical modification and further derivatization.
By studying this compound, researchers can gain insights into the design of new therapeutic agents. The fusion of aromaticity with aliphatic chains allows scientists to explore tailored properties that may optimize drug interaction profiles.
In conclusion, this compound exemplifies the intricate balance between chemical structure and biological function, making it a subject of great interest for future research in drug discovery.