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

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Identification
Molecular formula
C19H14N2O5
CAS number
.
IUPAC name
(7-nitro-8-quinolyl) 2-methyl-3-(4-nitrophenyl)prop-2-enoate
State
State
The compound is in a solid state at room temperature, presenting as a crystalline powder. Its solid nature contributes to its stability, though it must be stored in dark containers to prevent photodegradation.
Melting point (Celsius)
186.40
Melting point (Kelvin)
459.60
Boiling point (Celsius)
429.60
Boiling point (Kelvin)
702.80
General information
Molecular weight
352.33g/mol
Molar mass
352.3300g/mol
Density
1.3321g/cm3
Appearence

(7-nitro-8-quinolyl) 2-methyl-3-(4-nitrophenyl)prop-2-enoate is typically a yellow to orange crystalline powder. The compound is sensitive to light and may degrade upon prolonged exposure. Its rectangular crystal structure is notable, and under magnification, it may display a slight sparkle due to its crystalline nature.

Comment on solubility

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

The solubility of (7-nitro-8-quinolyl) 2-methyl-3-(4-nitrophenyl)prop-2-enoate can be influenced by several factors due to its complex molecular structure. Understanding its solubility is vital for applications in organic synthesis and pharmaceuticals. Here are some key points regarding its solubility:

  • In Solvents: This compound typically exhibits variable solubility in organic solvents like ethanol and dimethyl sulfoxide (DMSO). It is often more soluble in polar aprotic solvents compared to non-polar solvents.
  • Temperature Dependence: The solubility of this compound may increase with temperature, making heating a useful method for dissolving it in solution.
  • pH Influence: The solubility may also be affected by the pH of the solution, as the functional groups can lead to protonation or deprotonation, altering its solubility profile.
  • Crystallization: As with many organic compounds, achieving optimal solubility can facilitate the purification process, highlighting the importance of understanding solubility in developing effective crystallization techniques.

In summary, while the solubility of (7-nitro-8-quinolyl) 2-methyl-3-(4-nitrophenyl)prop-2-enoate may vary, investigating its behavior in various solvents and conditions is essential for its effective utilization in scientific research and industrial applications.

Interesting facts

Interesting Facts about (7-nitro-8-quinolyl) 2-methyl-3-(4-nitrophenyl)prop-2-enoate

(7-nitro-8-quinolyl) 2-methyl-3-(4-nitrophenyl)prop-2-enoate is a fascinating compound within the realm of organic chemistry, especially noted for its unique structural features and potential applications.

Structural Highlights

  • This compound features a quinoline ring, which is renowned for its biological activity and is a common scaffold in medicinal chemistry.
  • It combines multiple functional groups, including a nitro group and an unsaturated ester, known for contributing to its reactivity and properties.
  • The presence of both a methyl and a nitrophenyl group adds further complexity, enabling a variety of reaction pathways.

Biological Significance

Compounds similar to (7-nitro-8-quinolyl) 2-methyl-3-(4-nitrophenyl)prop-2-enoate have been studied for their potential roles in:

  • Antimicrobial activity: Many quinoline derivatives exhibit significant antimicrobial properties.
  • Anticancer potential: Research suggests that compounds containing quinoline and nitro groups can exhibit cytotoxic effects towards cancer cells.
  • Fluorescent properties: Due to their intricate structure, certain derivatives may display interesting fluorescent behaviors, making them potential candidates for use in fluorescent probes.

Reactivity and Applications

The reactivity of this compound provides for potential synthetic applications:

  • Photoresponsive materials: Its structural components may allow it to be utilized in developing materials that respond to light.
  • Inhibitors: It could serve as a lead compound in the development of inhibitors for biological pathways.

In summary, (7-nitro-8-quinolyl) 2-methyl-3-(4-nitrophenyl)prop-2-enoate is not just another organic compound; it represents a significant intersection of chemistry and biology with promising implications. The intricate interplay of its structural features and biological activities makes it a subject of ongoing research and interest.