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5-Phenylisoquinoline chloride

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Identification
Molecular formula
C15H12ClN
CAS number
2942-22-5
IUPAC name
5-phenylisoquinolin-2-ium;chloride
State
State

At room temperature, 5-Phenylisoquinoline chloride is in a solid state, typically found in crystalline form.

Melting point (Celsius)
161.00
Melting point (Kelvin)
434.15
Boiling point (Celsius)
275.00
Boiling point (Kelvin)
548.15
General information
Molecular weight
249.72g/mol
Molar mass
249.7190g/mol
Density
1.2250g/cm3
Appearence

5-Phenylisoquinoline chloride typically appears as a white to pale yellow crystalline solid.

Comment on solubility

Solubility of 5-phenylisoquinolin-2-ium chloride

The solubility of 5-phenylisoquinolin-2-ium;chloride, also known as a quaternary ammonium compound, showcases unique properties due to its structural characteristics.

Key factors influencing solubility include:

  • Polarity: The presence of the quaternary ammonium group typically enhances solubility in polar solvents, especially water.
  • Ionic Nature: As a chloride salt, it can often dissolve well in aqueous solutions as it dissociates into ions.
  • Hydrogen Bonding: The potential for hydrogen bonding with water molecules can further increase its solubility.

In general, quaternary ammonium chlorides are known for their good solubility in water and other polar solvents, making 5-phenylisoquinolin-2-ium;chloride likely to follow similar patterns.
However, the specific solubility can depend on various factors such as temperature and the presence of other ions in solution. It is always recommended to conduct empirical solubility tests for precise determination.

Interesting facts

Interesting Facts about 5-phenylisoquinolin-2-ium;chloride

5-phenylisoquinolin-2-ium;chloride is a fascinating compound with unique properties that make it a noteworthy subject of study in the field of organic chemistry. Here are some engaging insights:

  • Structure and Stability: This compound features an isoquinoline framework, which is a bicyclic structure that contains a nitrogen atom. Its stability is attributed to the resonance forms that contribute to its aromatic character. This makes it a good candidate for various chemical reactions.
  • Applications in Research: 5-phenylisoquinolin-2-ium;chloride plays a significant role in synthetic organic chemistry. It is often utilized in the development of new materials and can serve as a precursor in synthesizing more complex organic molecules.
  • Biological Activity: Compounds with isoquinoline structures have been studied for their biological activities. Research suggests that derivatives of this compound may exhibit antimicrobial and antifungal effects, making them valuable in pharmaceutical applications.
  • Fluorescence Properties: This compound has been observed to possess fluorescence properties, enabling it to be used in optical applications. Its ability to emit light upon excitation opens doors for its use in sensors and imaging technologies.
  • Synthetic Pathways: The synthesis of 5-phenylisoquinolin-2-ium;chloride can involve various techniques, including cyclization reactions. Understanding these pathways is essential for chemists aiming to modify the compound for specific applications.

In summary, the compound 5-phenylisoquinolin-2-ium;chloride represents an intersection of organic chemistry and applied sciences, with its diverse applications and interesting structural characteristics making it a subject of continuous research and exploration.

Synonyms
24464-07-1
DTXSID00947345
5-Phenylisoquinoline--hydrogen chloride (1/1)
RefChem:1073234
DTXCID301375605
5-Phenylisoquinoline hydrochloride
5-phenylisoquinolinium chloride
ISOQUINOLINE, 5-PHENYL-, HYDROCHLORIDE