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6,7-Dimethoxy-1-pentylisoquinoline

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Identification
Molecular formula
C16H23NO2
CAS number
27512-49-6
IUPAC name
6,7-dimethoxy-1-pentyl-isoquinoline
State
State

At room temperature, 6,7-Dimethoxy-1-pentylisoquinoline is in a liquid state.

Melting point (Celsius)
-15.00
Melting point (Kelvin)
258.15
Boiling point (Celsius)
305.00
Boiling point (Kelvin)
578.15
General information
Molecular weight
275.37g/mol
Molar mass
275.3740g/mol
Density
1.1120g/cm3
Appearence

6,7-Dimethoxy-1-pentylisoquinoline typically appears as a colorless to pale yellow liquid, depending on the purity and specific preparation conditions. It is moderately viscous and has a characteristic aromatic odor.

Comment on solubility

Solubility of 6,7-dimethoxy-1-pentyl-isoquinoline

The solubility of 6,7-dimethoxy-1-pentyl-isoquinoline can be particularly interesting due to its unique chemical structure and the presence of methoxy groups. Understanding its solubility profile can help predict its behavior in various environments.

Factors Affecting Solubility

This compound exhibits solubility characteristics influenced by several key factors:

  • Polarity: The presence of the methoxy groups may enhance the compound's overall polarity, affecting how it interacts with solvents.
  • Hydrophilicity vs. Hydrophobicity: The balance between the hydrophilic methoxy groups and the hydrophobic isoquinoline backbone plays a critical role in its solubility in polar or non-polar solvents.
  • Temperature: Like many organic compounds, solubility often increases with temperature; hence, this could be an important factor in solubility testing.
  • pH Levels: The ionization state of the compound may change in different pH environments, which can influence solubility in aqueous solutions.

In practical terms, 6,7-dimethoxy-1-pentyl-isoquinoline is likely to be more soluble in organic solvents such as ethanol or DMSO compared to water, primarily due to its hydrophobic characteristics stemming from the isoquinoline structure. For experimental purposes, it is advisable to test solubility in various solvents to confirm these theoretical predictions.

Conclusion

Understanding the solubility of 6,7-dimethoxy-1-pentyl-isoquinoline is essential for its application in medicinal chemistry and other fields, as it can impact bioavailability, formulation, and overall efficacy. As always, further experimental data will provide the most accurate insights.

Interesting facts

Interesting Facts about 6,7-Dimethoxy-1-pentyl-isoquinoline

6,7-Dimethoxy-1-pentyl-isoquinoline is a compound that piques the interest of both scientists and enthusiasts in the field of chemistry due to its unique structure and potential applications. Here are some intriguing aspects of this compound:

  • Structural Complexity: The presence of an isoquinoline skeleton combined with methoxy and pentyl side chains makes this compound particularly interesting. Its structural arrangement allows for various interactions and modifications, opening doors for further chemical exploration.
  • Psychoactive Properties: Isoquinolines are known for their diverse biological activities, including potential psychoactive effects. Some derivatives of isoquinoline structures have been studied for their interaction with neurotransmitter systems, suggesting possible therapeutic applications.
  • Synthetic Routes: The synthesis of 6,7-dimethoxy-1-pentyl-isoquinoline poses challenges and offers learning opportunities. Chemists often utilize innovative methods such as multicomponent reactions or ring closure reactions to create this compound, which can be a fascinating subject for students and researchers alike.
  • Research Interest: Due to its unique chemical characteristics, there is ongoing research exploring the implications of 6,7-dimethoxy-1-pentyl-isoquinoline in medicinal chemistry and pharmacology. This research may lead to the discovery of new therapeutic agents.
  • Fun Fact: Within the realm of organic compounds, isoquinolines have shown promising results in various drug discovery processes, amplifying the relevance of studying derivatives such as 6,7-dimethoxy-1-pentyl-isoquinoline.

In summary, the compound not only serves as an intriguing subject of study in chemistry but also fuels curiosity regarding its potential applications in the broader context of drug discovery and development. As such, it remains a fascinating focal point for both seasoned chemists and students eager to delve into the world of organic compounds.