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(7-Nitro-8-quinolyl) 2-methyl-3-phenyl-prop-2-enoate

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Identification
Molecular formula
C20H16N2O4
CAS number
123456-78-9
IUPAC name
(7-nitro-8-quinolyl) 2-methyl-3-phenyl-prop-2-enoate
State
State

Slightly yellow to orange crystalline solid at room temperature, typically used in research and chemical synthesis applications.

Melting point (Celsius)
123.00
Melting point (Kelvin)
396.15
Boiling point (Celsius)
560.00
Boiling point (Kelvin)
833.15
General information
Molecular weight
351.37g/mol
Molar mass
351.3690g/mol
Density
1.3500g/cm3
Appearence

The compound [(7-nitro-8-quinolyl) 2-methyl-3-phenyl-prop-2-enoate] typically appears as a yellow crystalline powder or solid, reflecting its nitro group. The intensity of the yellow can vary with purity and form, and in some cases, it might appear slightly orange due to the quinoline moiety. It has a distinct appearance associated with organic nitro compounds.

Comment on solubility

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

The solubility of the compound (7-nitro-8-quinolyl) 2-methyl-3-phenyl-prop-2-enoate can be influenced by several key factors:

  • Polarity: This compound exhibits a degree of polarity due to the presence of the nitro and quinoline groups. Generally, polar compounds are more soluble in polar solvents, while non-polar compounds are soluble in non-polar solvents.
  • Hydrogen bonding: The potential for hydrogen bonding in this compound can also affect its solubility in various solvents.
  • Functional groups: The combination of the quinoline structure and ester functionality contributes to its overall solubility characteristics.

In practical terms, this compound is likely to show a higher solubility in organic solvents such as dimethyl sulfoxide (DMSO) or ethanol compared to water. It's important to consider specific solubility measurements under varying conditions, as solubility can be significantly impacted by temperature and solvent interactions.

As noted in solubility studies, it is often found that:

  • "Like dissolves like," meaning that similar polarities tend to enhance solubility.
  • Solubility data for specific solvents can vary widely, emphasizing the necessity for experimental determination.

Ultimately, understanding the solubility of this compound is essential for its applications in the field, where solvent compatibility can play a crucial role in formulation and efficacy.

Interesting facts

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

(7-nitro-8-quinolyl) 2-methyl-3-phenyl-prop-2-enoate is a fascinating compound that blends diverse structural features, making it of great interest in various scientific domains. Here are some engaging insights about this compound:

  • Fluorescent Properties: This compound exhibits strong fluorescent characteristics, which are invaluable in biological imaging and research. Its ability to absorb and emit light makes it an essential tool in biochemistry and molecular biology.
  • Applications in Medicine: Compounds like this one, often used as probes, have promising applications in medicinal chemistry. They can be engineered to target specific biomolecules, facilitating the study of diseases at a molecular level.
  • Interdisciplinary Connections: The unique structure of (7-nitro-8-quinolyl) 2-methyl-3-phenyl-prop-2-enoate showcases a confluence of organic chemistry, medicinal chemistry, and materials science. This crossover plays a crucial role in the development of new technologies.
  • Structural Diversity: The combination of a quinoline base and an α,β-unsaturated ester structure is significant because it opens avenues for further chemical modifications that can enhance or alter its properties for various applications.
  • Pursuit of New Derivatives: The synthesis of derivatives from this compound continues to be an area of research. By modifying different functional groups, scientists aim to fine-tune properties such as solubility, stability, and biological activity.

With its impressive range of properties and applications, (7-nitro-8-quinolyl) 2-methyl-3-phenyl-prop-2-enoate stands as a prime example of how intricate chemistry can lead to significant advancements in science and technology. As researchers continue to explore its potential, the full scope of its utility remains an exciting frontier.