6,7-Dimethoxy-1-pentyl-3,4-dihydroisoquinoline

Identification

Molecular formula

C₁₆H₂₃NO₂

CAS number

10543-57-4

IUPAC name

6,7-dimethoxy-1-pentyl-3,4-dihydroisoquinoline

State

At room temperature, 6,7-Dimethoxy-1-pentyl-3,4-dihydroisoquinoline is in a liquid state.

Melting point (Celsius)

-17.50

Melting point (Kelvin)

255.65

Boiling point (Celsius)

274.30

Boiling point (Kelvin)

547.45

General information

Molecular weight

247.34g/mol

Molar mass

247.3390g/mol

Density

1.0023g/cm³

Appearence

6,7-Dimethoxy-1-pentyl-3,4-dihydroisoquinoline is typically a colorless to pale yellow liquid.

Comment on solubility

Solubility of 6,7-Dimethoxy-1-pentyl-3,4-dihydroisoquinoline

The solubility of 6,7-dimethoxy-1-pentyl-3,4-dihydroisoquinoline can present unique characteristics due to its complex structure and functional groups. Understanding its solubility profile is essential for applications in chemistry and pharmacology. Here are some key points regarding its solubility:

Polarity: The presence of methoxy groups likely contributes to some polar characteristics, which may enhance solubility in polar solvents such as water to a certain extent.
Solvent Compatibility: Generally, compounds with large hydrophobic alkyl chains tend to be more soluble in organic solvents like ethanol, methanol, or dimethyl sulfoxide (DMSO).
Temperature Influence: Solubility can be affected by temperature; with increased temperatures, many organic compounds tend to become more soluble.
pH Sensitivity: The solubility could vary with changes in pH, especially if the compound has functional groups that can ionize under different pH conditions.

In conclusion, the overall solubility of 6,7-dimethoxy-1-pentyl-3,4-dihydroisoquinoline is likely to depend on a delicate balance of its molecular structure and the nature of the solvent used. As with many organic compounds, experimental data is crucial for confirming these solubility assumptions.

Interesting facts

Interesting Facts About 6,7-Dimethoxy-1-pentyl-3,4-dihydroisoquinoline

6,7-Dimethoxy-1-pentyl-3,4-dihydroisoquinoline is a fascinating compound that has drawn the attention of researchers and chemists alike. Here are some compelling points about this intriguing chemical:

Structural Uniqueness: This compound belongs to the isoquinoline family, known for its complex ring structure. The presence of methoxy groups at the 6 and 7 positions adds to its versatility and potential reactivity.
Pharmacological Interest: Compounds in the isoquinoline class have been studied extensively for their biological activities, including their potential as analgesics, anti-inflammatory agents, and even in treating neurodegenerative diseases. The specific modifications in 6,7-dimethoxy-1-pentyl-3,4-dihydroisoquinoline may enhance these properties.
Role in Synthesis: The unique structure of this compound can serve as a starting point for synthesizing other complex molecules. Its dimethoxy and pentyl substitutions allow chemists to explore various synthetic routes and develop novel compounds for medicinal chemistry.
Natural Occurrence: Isoquinoline derivatives can be found in a variety of natural products. Investigating whether 6,7-dimethoxy-1-pentyl-3,4-dihydroisoquinoline can be isolated from natural sources is an exciting avenue for future research.
Potential Applications: With ongoing research, compounds like this may find applications in pharmacology, potentially leading to the development of new therapeutic agents or tools in drug discovery.

The intricate interplay of its chemical structure and biological potential makes 6,7-dimethoxy-1-pentyl-3,4-dihydroisoquinoline a standout compound worthy of study. As ongoing research continues to unveil the secrets of such compounds, the scientific community remains excited about the possibilities they hold in both academia and industry.