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

Identification

Molecular formula

C₁₉H₁₄N₂O₅

CAS number

100414-06-4

IUPAC name

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

State

At room temperature, this compound is in a solid state. It is stable and non-volatile, typically utilized in laboratory and possibly pharmaceutical applications.

Melting point (Celsius)

192.00

Melting point (Kelvin)

465.15

Boiling point (Celsius)

405.00

Boiling point (Kelvin)

678.15

General information

Molecular weight

354.33g/mol

Molar mass

354.3460g/mol

Density

1.3400g/cm³

Appearence

The compound typically appears as a yellow to orange crystalline solid. Its solid-state form reflects its aromatic conjugation and inherent stability from the nitro and methoxy substitutions on the ring structure.

Comment on solubility

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

The solubility of (7-nitro-8-quinolyl) 3-(4-methoxyphenyl)prop-2-enoate can be characterized as relatively low in common solvents, which is often a common trait among compounds with complex aromatic structures. Its solubility properties can be discussed in a few key points:

Polar vs. Nonpolar Solvents: This compound tends to be soluble in nonpolar organic solvents due to the hydrophobic character of its aromatic groups. Typical nonpolar solvents include hexane and chloroform.
Water Solubility: It is generally insoluble in water, which is noteworthy considering its molecular complexity and functional groups. The presence of both a nitro and quinoline moiety contributes to its limited interaction with polar solvents like water.
Effect of Temperature: Some organic compounds can exhibit increased solubility at elevated temperatures. While specific data for this compound is scarce, it is often the case that higher temperatures can promote greater dissolution in organic solvents.
Potential Applications: Understanding its solubility behavior is crucial when considering its applications in pharmaceuticals or materials science, where formulation in an appropriate solvent can enhance bioavailability or processing.

In conclusion, solubility plays a vital role in the usability of (7-nitro-8-quinolyl) 3-(4-methoxyphenyl)prop-2-enoate, governing its application in various chemical processes. As emphasized by many researchers, "A solubility profile can define the pathway for compound utilization." Therefore, studying its solubility in different solvents is essential for maximizing its potential in scientific applications.

Interesting facts

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

(7-nitro-8-quinolyl) 3-(4-methoxyphenyl)prop-2-enoate, often referred to in the scientific community as a complex organic compound, holds fascinating properties and applications. This compound, which features a unique structure that includes a quinoline moiety, is of significant interest in various fields, including medicinal chemistry and materials science. Here are some highlights:

Biological Activity: Studies suggest that quinoline derivatives exhibit a wide range of biological activities, including antimicrobial, antimalarial, and even anticancer properties. These potential applications make (7-nitro-8-quinolyl) 3-(4-methoxyphenyl)prop-2-enoate a subject of ongoing research.
Synthetic Versatility: The synthesis of this compound emphasizes the versatility of synthetic organic chemistry. Chemists appreciate the compound for its ability to be modified further, allowing the exploration of various analogs with potentially improved pharmacological properties.
Pivotal Role in Drug Discovery: The incorporation of the nitro group and the quinoline moiety represents a strategic approach often employed in drug design, significantly impacting the compound's reactivity and binding interactions with biological targets.
Material Science Applications: Beyond its medicinal potential, compounds like (7-nitro-8-quinolyl) 3-(4-methoxyphenyl)prop-2-enoate can serve as building blocks for advanced materials, particularly in creating sensors and dyes due to their unique electronic properties.
Research Opportunities: Research surrounding this compound is still evolving, offering numerous opportunities for chemists and biochemists to explore new reactions, properties, and applications.

As you delve into the study of this compound, consider not only its immediate benefits but also the broader implications of its research in both the pharmaceutical and material sciences. The excitement surrounding such compounds lies in their potential to lead to significant advancements across various fields.