(7-nitro-8-quinolyl) 3-(3-chlorophenyl)prop-2-enoate

Identification

Molecular formula

C₁₈H₁₁ClNO₄

CAS number

IUPAC name

(7-nitro-8-quinolyl) 3-(3-chlorophenyl)prop-2-enoate

State

This compound is typically a solid at room temperature, indicating a stable molecular structure and possibly a crystalline form.

Melting point (Celsius)

108.00

Melting point (Kelvin)

381.15

Boiling point (Celsius)

474.00

Boiling point (Kelvin)

747.15

General information

Molecular weight

370.78g/mol

Molar mass

370.7800g/mol

Density

1.3400g/cm³

Appearence

(7-Nitro-8-quinolyl) 3-(3-chlorophenyl)prop-2-enoate typically appears as a solid compound due to its complex organic structure. It may exhibit crystalline or powder form under standard laboratory conditions. The precise coloration can vary and might range from yellowish to off-white, depending on purity and specific sample history.

Comment on solubility

Solubility of (7-nitro-8-quinolyl) 3-(3-chlorophenyl)prop-2-enoate

The solubility of (7-nitro-8-quinolyl) 3-(3-chlorophenyl)prop-2-enoate can be influenced by various factors, making it an intriguing compound to study. Here are some key points regarding its solubility:

Solvent Compatibility: This compound typically demonstrates variable solubility across different solvents; it may be more soluble in organic solvents such as dimethyl sulfoxide (DMSO) and acetone.
Temperature Influence: Heating the solvent can enhance the solubility of the compound, which is a common phenomenon observed in many organic substances.
pH Sensitivity: As a compound with both a quinoline moiety and an ester functionality, its solubility might be affected by the pH of the solution, especially in aqueous environments.
Crystal Structure: The crystalline nature of the compound may impact its dissolution; a more crystalline solid often exhibits lower solubility.

In summary, understanding the solubility of (7-nitro-8-quinolyl) 3-(3-chlorophenyl)prop-2-enoate is essential for predicting its behavior in various chemical reactions and applications. It's vital to consider the solvent, temperature, pH, and crystalline structure for a comprehensive insight into its solubility profile.

Interesting facts

Interesting Facts about (7-nitro-8-quinolyl) 3-(3-chlorophenyl)prop-2-enoate

(7-nitro-8-quinolyl) 3-(3-chlorophenyl)prop-2-enoate is a fascinating compound with a unique structure and intriguing properties. Here are some enlightening facts about it:

Pharmacological Potential: This compound belongs to a class of chemicals known for their biological activities. It has been studied for its potential applications in medicinal chemistry, particularly in the development of anti-cancer agents and antimicrobial properties.
Structural Significance: The presence of the quinoline ring system in its structure makes it interesting. Quinoline derivatives have been extensively researched for their diverse pharmacological activities, including anti-inflammatory and anti-viral effects.
Electrophilic Reactivity: The nitro group at position 7 of the quinoline ring enhances the compound's electrophilic character, potentially increasing its reactivity in various chemical reactions, especially in nucleophilic substitutions.
Research Applications: This compound is often utilized in laboratory settings for synthetic organic chemistry research. Its reactivity makes it a useful intermediate for synthesizing other complex molecules.
Analytical Studies: Due to its unique composition, it serves as a subject in analytical chemistry, where researchers explore methods for its detection and quantification in various samples.

The study of (7-nitro-8-quinolyl) 3-(3-chlorophenyl)prop-2-enoate opens up numerous avenues in scientific research and application. As noted by one researcher, *"Compounds like these not only expand our understanding of chemical reactivity but also bring us one step closer to innovative therapeutics."*
Continued exploration of such compounds is essential for advancing our knowledge in both chemistry and medicine.