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6,7-dimethoxy-2-pentyl-3,4-dihydroisoquinoline

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Identification
Molecular formula
C16H25NO2
CAS number
2097-18-9
IUPAC name
6,7-dimethoxy-2-pentyl-3,4-dihydro-1H-isoquinoline
State
State

At room temperature, 6,7-dimethoxy-2-pentyl-3,4-dihydro-1H-isoquinoline is typically a solid. Its physical state can shift to a liquid upon slight heating due to its relatively low melting point.

Melting point (Celsius)
57.00
Melting point (Kelvin)
330.15
Boiling point (Celsius)
327.00
Boiling point (Kelvin)
600.15
General information
Molecular weight
261.36g/mol
Molar mass
261.3550g/mol
Density
1.0456g/cm3
Appearence

6,7-Dimethoxy-2-pentyl-3,4-dihydro-1H-isoquinoline typically appears as an off-white to pale yellow solid, depending on its purity. It is a crystalline compound that may be available in powder form.

Comment on solubility

Solubility of 6,7-Dimethoxy-2-pentyl-3,4-dihydro-1H-isoquinoline

The solubility of 6,7-dimethoxy-2-pentyl-3,4-dihydro-1H-isoquinoline in various solvents is an intriguing topic due to its complex molecular structure. Understanding solubility is essential for applications in pharmacology and organic chemistry. Here are some key points regarding its solubility:

  • Polarity: The presence of methoxy groups enhances polarity, which may contribute to solubility in polar solvents like water or methanol. However, due to the larger hydrophobic pentyl chain, solubility in nonpolar solvents is also probable.
  • Temperature Dependence: Solubility can vary significantly with temperature, often increasing at elevated temperatures due to higher kinetic energy, facilitating solvation.
  • pH Sensitivity: The solubility may also be affected by the pH of the solution, with potential ionization at certain pH levels, leading to changes in solubility behavior.

In summary, the solubility of 6,7-dimethoxy-2-pentyl-3,4-dihydro-1H-isoquinoline is influenced by its molecular characteristics, solvent type, and environmental conditions. As with many organic compounds, predicting solubility requires a comprehensive understanding of these factors.

Interesting facts

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!

Synonyms
CHEMBL4292641
SCHEMBL10315942
BDBM50464785