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No common name

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Identification
Molecular formula
C14H23NO2
CAS number
16459-85-7
IUPAC name
6,7-dimethoxy-2,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-2-ium
State
State

At room temperature, this compound is generally found in a solid state.

Melting point (Celsius)
156.00
Melting point (Kelvin)
429.15
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.15
General information
Molecular weight
235.33g/mol
Molar mass
235.3270g/mol
Density
1.2459g/cm3
Appearence

The compound generally appears as a solid at room temperature. Its specific color and crystalline structure may vary depending on its purity and form.

Comment on solubility

Solubility of 6,7-dimethoxy-2,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-2-ium

The solubility of 6,7-dimethoxy-2,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-2-ium in various solvents can be quite intriguing due to its unique structural characteristics. Here are some key points to consider:

  • Polarity: The presence of methoxy groups (–OCH3) suggests moderate polarity, which can enhance solubility in polar organic solvents.
  • Hydrophobic regions: The multiple methyl groups contribute to hydrophobic interactions, influencing solubility behavior in non-polar solvents.
  • pH sensitivity: As a quaternary ammonium ion, this compound may exhibit varied solubility depending on the pH of the solution, potentially favoring solubility in alkaline environments.
  • Solvent selection: It is likely to be soluble in solvents such as:
    • Alcohols (e.g., methanol, ethanol)
    • Chloroform
    • Aqueous bases

In summary, the solubility of 6,7-dimethoxy-2,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-2-ium is influenced by both its polar and non-polar functional groups, making it favorable in specific non-aqueous solvents while potentially being versatile in alkaline solutions.

Interesting facts

Interesting Facts about 6,7-Dimethoxy-2,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-2-ium

The compound 6,7-dimethoxy-2,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-2-ium belongs to a fascinating class of organic molecules known as isoquinolines. These compounds are characterized by a six-membered aromatic ring fused to a five-membered nitrogen-containing ring.

Key Characteristics:

  • Diverse Applications: Isoquinolines are versatile structures often found in various natural products and medicinal compounds. They have been studied for their potential therapeutic properties, including antimicrobial and anti-cancer activities.
  • Structural Composition: The presence of multiple methyl and methoxy groups in this compound enhances its complexity and significantly influences its reactivity and stability. These substituents can alter the electronic properties of the molecule, impacting its behavior in biological systems.
  • Research Interest: Compounds like this isoquinolinium derivative are of interest in the field of synthetic organic chemistry. Researchers are continually exploring methods to synthesize these compounds efficiently, often leading to new synthetic strategies and insights into molecular design.
  • Synthesis Pathways: The synthesis of such isoquinolinium compounds generally involves innovative methods, including cyclization reactions and the use of various catalysts to facilitate the formation of the isoquinoline skeleton.

A Scientific Perspective:

For students and budding chemists, studying compounds like 6,7-dimethoxy-2,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-2-ium is invaluable. They not only provide insight into chemical reactivity and mechanisms but also contribute to a broader understanding of how structural modifications can impact bioactivity. As one famous chemist once said, "Chemistry is the science of transformation, allowing us to manipulate molecules for the betterment of society." This compound serves as a compelling example of such transformation and its potential applications in healthcare and pharmaceuticals.