Sodium 2-phenylquinoline-4-carboxylate

Identification

Molecular formula

C₁₆H₁₀NNaO₂

CAS number

22318-61-2

IUPAC name

sodium;2-phenylquinoline-4-carboxylate

State

At room temperature, sodium 2-phenylquinoline-4-carboxylate is typically a solid. It is stable under normal conditions but should be stored in a cool, dry place to maintain its stability and efficacy.

Melting point (Celsius)

220.00

Melting point (Kelvin)

493.15

Boiling point (Celsius)

315.00

Boiling point (Kelvin)

588.15

General information

Molecular weight

285.30g/mol

Molar mass

285.2980g/mol

Density

1.2350g/cm³

Appearence

The compound typically appears as a crystalline powder. Its color may range from off-white to a pale yellow, depending on its purity and specific structure.

Comment on solubility

Solubility of Sodium 2-Phenylquinoline-4-Carboxylate

Sodium 2-phenylquinoline-4-carboxylate, a salt formed from the carboxylic acid and sodium, exhibits intriguing solubility characteristics that are worth exploring:

Soluble in Water: Due to the presence of the sodium ion and the carboxylate group, sodium 2-phenylquinoline-4-carboxylate is generally soluble in water. This characteristic can be attributed to the ion-dipole interactions between the sodium ions and water molecules.
Polarity Effect: The polar nature of the carboxylate group increases its ability to interact with polar solvents, further enhancing its solubility in such environments.
Organic Solvents: Although primarily soluble in water, this compound may show limited solubility in non-polar organic solvents, owing to its relatively large hydrophobic phenyl group.
pH Dependency: The solubility can also be influenced by the pH of the solution; in more alkaline environments, the anionic form is more prevalent, promoting higher solubility.

In summary, the solubility profile of sodium 2-phenylquinoline-4-carboxylate illustrates the interplay between its molecular structure and environmental conditions:

High solubility in water due to ionic and polar interactions.
Limited solubility in non-polar solvents, underscoring the impact of hydrophobic character.

Understanding the solubility of this compound is crucial for its applications in various fields, such as medicinal chemistry and materials science.

Interesting facts

Interesting Facts about Sodium 2-Phenylquinoline-4-Carboxylate

Sodium 2-phenylquinoline-4-carboxylate is a fascinating compound owing to its unique chemical structure and potential applications in various fields. Here are some compelling aspects to consider:

Structural Diversity: This compound belongs to the quinoline family, which is known for its complex ring structures. Its architecture is not only aesthetically appealing but also contributes to its chemical reactivity.
Biological Activity: Compounds like sodium 2-phenylquinoline-4-carboxylate have been studied for their potential antimicrobial and antioxidant properties. Such activities make them of high interest in medicinal chemistry.
Synthetic Pathways: The synthesis of sodium 2-phenylquinoline-4-carboxylate involves intriguing organic reactions, showcasing the importance of understanding organic synthesis techniques for generating complex molecules.
Potential Uses: Beyond their biological implications, compounds in the quinoline family are often explored for applications in materials science, including their roles as dyes or catalysts.
Research Opportunities: The unique characteristics of sodium 2-phenylquinoline-4-carboxylate present numerous avenues for further research. Scientists are continually uncovering new aspects of its reactivity and utility in different fields, from pharmaceuticals to organic electronics.

As a scientist, the study of compounds like sodium 2-phenylquinoline-4-carboxylate underscores the intricate connections between molecular structure and function. Such relationships are central to the ongoing advancement of both theoretical and applied chemistry.