6,7-dimethoxy-2-pentyl-3,4-dihydroisoquinoline
- Molecular formula
- C16H25NO2
- CAS Number
- 2097-18-9
- IUPAC Name
- 6,7-dimethoxy-2-pentyl-3,4-dihydro-1H-isoquinoline
- Molecular Weight
- 261.36g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.0456g/cm3
- Synonyms
- CHEMBL4292641
Identification
Interesting Facts about 6,7-Dimethoxy-2-pentyl-3,4-dihydro-1H-isoquinoline
6,7-Dimethoxy-2-pentyl-3,4-dihydro-1H-isoquinoline is a fascinating compound that belongs to the isoquinoline family, which consists of bicyclic organic compounds featuring a benzene ring fused to a pyridine ring. This particular compound has sparked interest among researchers due to its various potential applications and unique structural properties.
Key Features
- Pharmacological Potential: Compounds in the isoquinoline class have been associated with a range of biological activities, including antimicrobial, anti-inflammatory, and anticancer properties. Research into this compound may yield insights beneficial for medical science.
- Structural Diversity: The presence of methoxy groups provides additional reactivity and potential for functionalization, making it an attractive subject for synthetic chemists aiming to explore new derivatives.
- Neuroscientific Implications: Isoquinolines often have neuroactive effects, which could suggest potential pathways for drug development targeting neurological disorders or enhancing cognitive function.
As noted by scientists, “The diversity within isoquinoline derivatives opens up a plethora of opportunities for exploration in medicinal chemistry.” This emphasizes the need for ongoing research into such compounds to fully understand their mechanisms and potential.
Applications and Research Directions
In addition to its potential role in pharmaceuticals, 6,7-dimethoxy-2-pentyl-3,4-dihydro-1H-isoquinoline can be valuable in:
- Synthetic Organic Chemistry: Utilizing its structural framework to design more complex molecules.
- Natural Product Synthesis: Exploring its synthesis in the context of natural product chemistry.
- Chemical Biology: Investigating its interactions with biological targets, leading to novel therapeutic strategies.
This compound exemplifies how even seemingly simple chemical structures can lead to significant discoveries and applications. Continued exploration into such compounds may inspire future innovations in various scientific fields!