Interesting facts
Interesting Facts About (7-nitro-8-quinolyl) 2-oxochromene-3-carboxylate
(7-nitro-8-quinolyl) 2-oxochromene-3-carboxylate is a fascinating compound that has garnered interest in various fields, particularly in medicinal chemistry and organic synthesis. Here are some engaging insights about this intriguing molecule:
- Origin of the Name: The compound's name reveals its structural components, highlighting the presence of a nitro group and quinoline derivative along with chromene and carboxylate functionalities. Each fragment hints at its unique chemical properties.
- Fluorescent Properties: Compounds within the chromene family often exhibit interesting photophysical properties. These features make them valuable for applications in fluorescence imaging and sensors.
- Bioactivity: The presence of the quinoline moiety in this compound has been linked to various biological activities, including antimicrobial and anticancer properties, making it a potential candidate for drug development.
- Synthetic Versatility: The methodology used to synthesize such compounds often involves intricate organic reactions. This molecule can serve as an important intermediate in the synthesis of more complex organic materials.
- Potential Applications: Research continues to explore the use of (7-nitro-8-quinolyl) 2-oxochromene-3-carboxylate in the fields of organic electronics, particularly in the creation of organic light-emitting diodes (OLEDs) and photovoltaic devices.
In conclusion, (7-nitro-8-quinolyl) 2-oxochromene-3-carboxylate showcases the remarkable intersection of chemistry and application, providing a rich area for study and innovation. As scientists delve deeper into its properties and applications, this compound is likely to hold significant promise for future developments in both industry and research.
Synonyms
BRN 1555008
2H-1-BENZOPYRAN-3-CARBOXYLIC ACID, 2-OXO-, 7-NITRO-8-QUINOLINYL ESTER
29007-40-7
DTXSID70183253
2-Oxo-2H-1-benzopyran-3-carboxylic acid 7-nitro-8-quinolinyl ester
RefChem:268333
DTXCID80105744
Solubility of (7-nitro-8-quinolyl) 2-oxochromene-3-carboxylate
The solubility of the compound (7-nitro-8-quinolyl) 2-oxochromene-3-carboxylate can be quite intriguing due to its unique molecular structure. Understanding its solubility behavior is critical for applications in various chemical and pharmaceutical processes.
Key Factors Influencing Solubility:
As a general observation, compounds similar to (7-nitro-8-quinolyl) 2-oxochromene-3-carboxylate are often more soluble in organic solvents than in water, largely attributed to their aromatic character, which can decrease solubility in polar solvents like water. However, it's essential to conduct experimental evaluations to determine its exact solubility profile under various conditions.
In conclusion, while the precise solubility of (7-nitro-8-quinolyl) 2-oxochromene-3-carboxylate can depend on multiple factors, it is clear that its intricate structure presents opportunities for tailored solubility in both organic and aqueous environments, making it a subject of interest in both research and application domains.