DMAPN
- Molecular formula
- C25H31NO2
- CAS Number
- 54932-56-4
- IUPAC Name
- phenyl 5-(dimethylamino)-2-isopropyl-2-(1-naphthyl)pentanoate
- Molecular Weight
- 353.50g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.0200g/cm3
- Synonyms
- 6779-74-4
Identification
Interesting Facts about Phenyl 5-(Dimethylamino)-2-Isopropyl-2-(1-Naphthyl)pentanoate
Pursuing the complexities of chemical compounds can often lead to the discovery of fascinating insights and applications. One such compound, phenyl 5-(dimethylamino)-2-isopropyl-2-(1-naphthyl)pentanoate, is a notable entity in the field of organic chemistry.
Structural Characteristics
This compound exhibits a unique structure characterized by:
- Phenyl Group: The presence of a phenyl group contributes to the compound’s hydrophobic properties, making it an intriguing candidate for various applications.
- Dimethylamino Group: The dimethylamino group confers basicity, allowing potential interactions in biological systems.
- Naphthyl Substituent: The naphthyl part adds aromatic character, influencing the compound's reactivity and stability.
Biological Relevance
This compound is of particular interest due to its potential applications in pharmacology. Here are some areas where it might play a role:
- Pharmaceutical Development: The unique structure may contribute to the development of novel therapeutics.
- Research in Neuroscience: The dimethylamino group suggests a possible activity related to neurotransmission, making it a subject of interest in studies of psychotropic compounds.
- Drug Design: The compound can serve as a lead structure or motif in designing new drugs targeting specific biological pathways.
Conclusion
In summary, phenyl 5-(dimethylamino)-2-isopropyl-2-(1-naphthyl)pentanoate stands out not only for its interesting synthetic attributes but also for its potential contributions to various scientific fields. As research into organic compounds continues to evolve, this compound may well unlock new avenues in both understanding and application.