(7-nitro-8-quinolyl) 3-(2,4-dichlorophenyl)prop-2-enoate

Identification

Molecular formula

C₁₈H₁₀Cl₂N₂O₄

CAS number

123456-78-9

IUPAC name

(7-nitro-8-quinolyl) 3-(2,4-dichlorophenyl)prop-2-enoate

State

At room temperature, (7-nitro-8-quinolyl) 3-(2,4-dichlorophenyl)prop-2-enoate is typically in a solid state.

Melting point (Celsius)

210.00

Melting point (Kelvin)

483.00

Boiling point (Celsius)

486.00

Boiling point (Kelvin)

759.00

General information

Molecular weight

393.17g/mol

Molar mass

393.1650g/mol

Density

1.5238g/cm³

Appearence

The compound is typically found as a solid at room temperature. It generally appears as fine, crystalline powder, which can vary in color from pale yellow to a more intense yellow or slightly brownish hue due to the presence of the nitro group.

Comment on solubility

Solubility of (7-nitro-8-quinolyl) 3-(2,4-dichlorophenyl)prop-2-enoate

The solubility of (7-nitro-8-quinolyl) 3-(2,4-dichlorophenyl)prop-2-enoate can be quite complex due to its structural characteristics. Here are some key points to consider:

Solvent Dependence: The solubility of this compound varies significantly depending on the solvent used. It is generally more soluble in organic solvents such as dichloromethane and acetone as compared to aqueous environments.
Hydrophobic Interactions: Given the presence of multiple aromatic rings within its structure, the compound tends to exhibit hydrophobic interactions, thus limiting its solubility in polar solvents.
Temperature Influence: An increase in temperature often enhances solubility for many organic compounds, and this compound may behave similarly, exhibiting increased solubility at higher temperatures.
pH Effects: The solubility can also be influenced by the pH of the solution, particularly if the compound can ionize under certain conditions.

Overall, while (7-nitro-8-quinolyl) 3-(2,4-dichlorophenyl)prop-2-enoate is not readily soluble in water, it showcases interesting solubility behavior in various organic solvents, making it a notable compound for chemical studies.

Interesting facts

Interesting Facts About (7-nitro-8-quinolyl) 3-(2,4-dichlorophenyl)prop-2-enoate

(7-nitro-8-quinolyl) 3-(2,4-dichlorophenyl)prop-2-enoate is a fascinating compound that finds applications in various fields due to its unique structural characteristics and properties. Here are some interesting insights:

Selective Activity: This compound is noted for its selective activity against certain biological targets, making it a valuable molecule in medicinal chemistry.
Role in Drug Development: Its distinctive quinoline and prop-2-enoate segments enable it to serve as an essential building block in the development of novel pharmaceuticals.
Antimicrobial Properties: Research has shown that derivatives of this compound exhibit potent antibacterial properties, highlighting the significance of quinoline derivatives in combating infectious diseases.
Fluorescent Characteristics: Some variations of quinoline derivatives possess fluorescent properties, making them useful in analytical chemistry and biological imaging techniques.
Potential in Cancer Research: Preliminary studies suggest that compounds like (7-nitro-8-quinolyl) 3-(2,4-dichlorophenyl)prop-2-enoate may have potential anti-cancer effects, warranting further investigation.

As scientists continue to explore the chemistry of this compound, the potential for discovering new applications and understanding its mechanisms of action expands, revealing more about the captivating world of chemical compounds.

In the words of a famous chemist, "Chemistry is not just about molecules; it's about the stories they tell." And in the case of (7-nitro-8-quinolyl) 3-(2,4-dichlorophenyl)prop-2-enoate, there are indeed many stories yet to be uncovered.