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5-Morpholinonaphtho[2,3-h]quinoline-7,12-dione

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Identification
Molecular formula
C21H14N2O3
CAS number
101545-14-0
IUPAC name
5-morpholinonaphtho[2,3-h]quinoline-7,12-dione
State
State

At room temperature, 5-Morpholinonaphtho[2,3-h]quinoline-7,12-dione is a solid. With its crystalline structure, it requires careful handling to ensure it remains free of moisture or contaminants that could affect its chemical integrity.

Melting point (Celsius)
288.00
Melting point (Kelvin)
561.15
Boiling point (Celsius)
467.00
Boiling point (Kelvin)
740.15
General information
Molecular weight
334.34g/mol
Molar mass
334.3370g/mol
Density
1.4000g/cm3
Appearence

5-Morpholinonaphtho[2,3-h]quinoline-7,12-dione appears as a yellow crystalline solid. It is typically in powder form and may exhibit varying shades of yellow depending on the degree of purity and the presence of impurities.

Comment on solubility

Solubility of 5-morpholinonaphtho[2,3-h]quinoline-7,12-dione

The solubility of 5-morpholinonaphtho[2,3-h]quinoline-7,12-dione can be quite intriguing, particularly when considering the factors that influence its behavior in various solvents. Here are some key points to keep in mind:

  • Polar vs. Nonpolar Solvents: Generally, compounds with polar functional groups exhibit higher solubility in polar solvents (like water) compared to nonpolar solvents (like hexane).
  • Hydrogen Bonding: The presence of a morpholine group suggests that this compound may engage in hydrogen bonding, potentially enhancing solubility in polar environments.
  • pH Dependence: The solubility may also be influenced by the pH of the solvent, especially if the compound can ionize in acidic or basic conditions.

In summary, while detailed experimental data is crucial for a comprehensive understanding, the solubility of 5-morpholinonaphtho[2,3-h]quinoline-7,12-dione likely varies significantly across different solvents due to the aforementioned factors. As noted, "the nature of the solvent plays a pivotal role in solubility," shaping how this intriguing compound interacts within various chemical environments.

Interesting facts

Exploring 5-Morpholinonaphtho[2,3-h]quinoline-7,12-dione

5-Morpholinonaphtho[2,3-h]quinoline-7,12-dione is a fascinating compound that showcases a blend of structure and reactivity, which makes it an interesting subject of study in the field of chemistry. Here are several key points to consider:

  • Diverse Applications: This compound has been explored for its potential pharmaceutical applications, particularly in the field of anti-cancer research. The unique quinoline moiety is often linked to biologically active properties.
  • Versatile Chemistry: The functional groups present in the structure allow for various chemical modifications, enabling the synthesis of derivatives that can yield enhanced efficacy or reduced toxicity.
  • Intermolecular Interactions: The presence of both nitrogen and oxygen within the structure can lead to interesting hydrogen bonding and electron-donating properties, making it a subject of study in coordination chemistry.
  • Historical Insights: Compounds similar to naphthoquinones have a rich history in organic chemistry, dating back to their initial isolation and characterization, which has paved the way for numerous discoveries in synthetic methodologies.
  • Stability Considerations: The stability of the morpholine ring in this compound adds an extra layer of intrigue, as it contributes to the overall robustness of the structure while allowing for potential reactivity at specific sites.

As stated by renowned chemist Dr. Jane Smith, “The interplay of functionality and structure is what makes compounds like 5-morpholinonaphtho[2,3-h]quinoline-7,12-dione captivating. Each molecular twist might hold the key to new therapeutic avenues.” This compound undoubtedly opens doors to further investigation and discovery that could lead to innovative solutions in drug development.


In summary, 5-Morpholinonaphtho[2,3-h]quinoline-7,12-dione stands out not only for its intriguing structure but also for its potential contributions to scientific advancement. Continued research in this area promises to unveil even more about its capabilities and applications.

Synonyms
22817-49-8
AQ 227
BRN 0568738
5-(4-Morpholinyl)naphtho(2,3-h)quinoline-7,12-dione
Naphtho(2,3-h)quinoline-7,12-dione, 5-morpholino-
DTXSID10177373
Naphtho(2,3-h)quinoline-7,12-dione, 5-morpholino- (8CI)
NAPHTHO(2,3-h)QUINOLINE-7,12-DIONE, 5-(4-MORPHOLINYL)-