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

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Identification
Molecular formula
C19H13N3O6
CAS number
123456-78-9
IUPAC name
(7-nitro-8-quinolyl) 2-methyl-3-(2-nitrophenyl)prop-2-enoate
State
State

At room temperature, the compound is in a solid state, appearing as yellow crystals.

Melting point (Celsius)
260.00
Melting point (Kelvin)
533.15
Boiling point (Celsius)
500.00
Boiling point (Kelvin)
773.15
General information
Molecular weight
370.34g/mol
Molar mass
370.3410g/mol
Density
1.4000g/cm3
Appearence

(7-nitro-8-quinolyl) 2-methyl-3-(2-nitrophenyl)prop-2-enoate appears as a yellow crystalline solid.

Comment on solubility

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

The solubility of (7-nitro-8-quinolyl) 2-methyl-3-(2-nitrophenyl)prop-2-enoate is a crucial aspect that influences its applications and effectiveness in various chemical contexts. Generally, the solubility of a compound can be influenced by factors such as:

  • Polarity: This compound exhibits a degree of polarity due to the presence of nitro and quinoline functional groups, which can enhance its solubility in polar solvents.
  • Hydrogen Bonding: The ability to form hydrogen bonds may lead to improved solubility in protic solvents.
  • Temperature: As with many organic compounds, solubility often increases with temperature, making it important to consider temperature during solubility tests.
  • Solvent Choice: Common solvents for similar compounds include ethanol, methanol, and DMSO; however, the specific solubility in these solvents can vary widely.

It is often noted that “like dissolves like”, meaning that polar compounds tend to dissolve well in polar solvents. Therefore, in cases where solubility is limited, one might consider exploring different solvent systems to find the most effective dissolution medium. Additionally, solubility can markedly affect the biological activity of compounds, particularly in pharmacological studies.

In summary, while the solubility profile of (7-nitro-8-quinolyl) 2-methyl-3-(2-nitrophenyl)prop-2-enoate may present challenges, careful consideration of the factors mentioned above can lead to successful applications in various scientific fields.

Interesting facts

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

(7-Nitro-8-quinolyl) 2-methyl-3-(2-nitrophenyl)prop-2-enoate is a fascinating compound that plays an important role in various fields of research and application. Here are some key points that highlight its significance:

  • Structural Complexity: This compound features a complex structure that includes a nitro-substituted quinoline moiety fused with a phenyl group. The interplay of various functional groups contributes to its unique chemical properties.
  • Biological Activity: Research has indicated that compounds similar to (7-nitro-8-quinolyl) derivatives can exhibit significant biological activities, including antibacterial and antitumor properties. This makes it a valuable candidate for pharmaceutical development.
  • Potential Applications: The compound may find applications in the fields of organic synthesis and medicinal chemistry. Its structural features can be exploited to design new drugs and explore novel therapeutic pathways.
  • Fluorescence Properties: Many quinoline derivatives, including this compound, are known for their interesting fluorescence properties. These characteristics make them suitable for use as fluorescent probes in biological and chemical sensing applications.
  • Research Significance: The study of such compounds not only enhances our understanding of organic chemistry but also paves the way for the discovery of new methodologies in synthesizing complex molecules.

In summary, (7-nitro-8-quinolyl) 2-methyl-3-(2-nitrophenyl)prop-2-enoate is more than just a chemical compound; it is a bridge to understanding complex interactions within biological systems and offers potential for innovative applications in science and medicine.