2,3-dimethyl-7-phenylisoquinolinium

Identification

Molecular formula

C₁₉H₁₈N⁺

CAS number

4876-31-5

IUPAC name

2,3-dimethyl-7-phenyl-isoquinolin-2-ium

State

This compound is typically found as a solid at room temperature, indicating a well-organized crystalline structure. It does not readily melt or vaporize under normal atmospheric conditions, which suggests a fairly high melting and boiling point.

Melting point (Celsius)

267.00

Melting point (Kelvin)

540.00

Boiling point (Celsius)

570.00

Boiling point (Kelvin)

843.00

General information

Molecular weight

281.36g/mol

Molar mass

281.3590g/mol

Density

1.0200g/cm³

Appearence

2,3-Dimethyl-7-phenylisoquinolinium typically forms crystalline solids that can range in color from pale yellow to white. These crystals are generally shiny and exhibit a needle-like or amorphous formation, depending on the method of crystallization.

Comment on solubility

Solubility of 2,3-dimethyl-7-phenyl-isoquinolin-2-ium

The solubility of 2,3-dimethyl-7-phenyl-isoquinolin-2-ium is an intriguing aspect of its chemical behavior, influenced by various factors such as molecular structure, polarity, and temperature.

Factors Influencing Solubility

Polarity: The hydrophilicity or hydrophobicity of the compound plays a crucial role in determining its solubility in water or organic solvents. Isoquinolinium compounds often exhibit varying levels of polarity that can affect their solubility.
Temperature: Increased temperatures can lead to higher solubility for many compounds, including organic salts like this isoquinolinium derivative.
Interactions: The presence of functional groups may allow for hydrogen bonding or ionic interactions, enhancing solubility in specific solvents.

Typically, salts of isoquinolinium compounds tend to be soluble in polar solvents, while their neutral forms can show limited solubility. While detailed solubility data might not be readily available for 2,3-dimethyl-7-phenyl-isoquinolin-2-ium, it is essential to consider the general trends and the chemical environment when evaluating its solubility potential.

In conclusion, understanding solubility behaviors offers valuable insights into the application and synthesis of 2,3-dimethyl-7-phenyl-isoquinolin-2-ium, guiding researchers in selecting suitable solvents for reactions and extractions.

Interesting facts

Interesting Facts about 2,3-Dimethyl-7-phenyl-isoquinolin-2-ium

The compound 2,3-dimethyl-7-phenyl-isoquinolin-2-ium belongs to a fascinating class of compounds known as isoquinolines, which are derived from isoquinoline structures. These compounds have garnered interest due to their unique molecular configurations and biological activities.

Significance in Research

Medicinal Potential: Compounds related to isoquinolines, including this one, have been studied for their potential therapeutic activities. They exhibit a range of biological properties such as antimicrobial, anti-inflammatory, and anticancer effects.
Role in Organic Synthesis: Isoquinoline derivatives serve as valuable intermediates in the synthesis of more complex organic molecules. Their reactivity opens doors to various chemical transformations.
Pharmacophore Models: The specific arrangement of methyl and phenyl groups in 2,3-dimethyl-7-phenyl-isoquinolin-2-ium makes it an interesting candidate for studying structure-activity relationships in drug design.

Chemical Properties

While the chemical formula reveals its structure, the unique properties of the compound can lead to intriguing behaviors in different environments. Salts formed from such isoquinoline compounds often exhibit varied solubility in solvents, which can affect their overall utility in different applications.

Fun Fact

A notable aspect of isoquinoline derivatives is their colorful history in traditional medicine systems. Many similar compounds have been utilized for centuries in herbal remedies, showcasing the importance of studying such compounds to understand their historical and cultural significance.

As you delve deeper into this fascinating compound, remember that every structural variation, like the additions of methyl and phenyl groups, can dramatically influence its chemical behavior and potential applications in modern science!