6,7-Dimethoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline
- Molecular formula
- C12H17NO2
- CAS Number
- 33385-61-0
- IUPAC Name
- 6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinoline
- Molecular Weight
- 191.25g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1320g/cm3
- Synonyms
- 6, 7-DIMETHOXY-2-METHYL-1, 2, 3, 4-TETRAHYDRO-ISOQUINOLINE
Identification
Interesting Facts about 6,7-Dimethoxy-2-methyl-3,4-dihydro-1H-isoquinoline
6,7-Dimethoxy-2-methyl-3,4-dihydro-1H-isoquinoline is a fascinating chemical compound that belongs to a class of compounds known as isoquinolines. This particular isoquinoline derivative holds significant interest in various fields, especially in medicinal and organic chemistry. Here are some notable points:
- Natural Product Potential: Isoquinolines are often found in numerous natural products and alkaloids, which can exhibit diverse biological activities. This compound's structure suggests potential pharmacological properties, making it a subject of interest in drug discovery.
- Synthetic Versatility: The synthesis of 6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinoline provides an excellent example of complex organic synthesis techniques. Understanding the reaction pathways and mechanisms involved enhances a chemist's toolkit for creating similar compounds.
- Biological Interest: Compounds containing isoquinoline structures have been studied for their effects on the central nervous system. Some derivatives have shown promise as potential treatments for neurological disorders.
- Research Applications: This isoquinoline derivative can serve as a precursor in the synthesis of various bioactive molecules, aiding in the exploration of new medicinal agents.
- Structure-Activity Relationship (SAR): The presence of methoxy groups in the structure may influence the compound's reactivity and biological activity, offering chemists avenues to explore structure-activity relationships further.
In summary, 6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinoline displays a rich tapestry of chemical properties and potential applications. Its study not only contributes to our understanding of isoquinoline chemistry but also opens up exciting possibilities in medicinal chemistry and drug development. As a compound that bridges organic synthesis and biological activity, it remains an intriguing topic for both researchers and students alike.