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(7-nitro-8-quinolyl) furan-2-carboxylate

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Identification
Molecular formula
C14H8N2O5
IUPAC name
(7-nitro-8-quinolyl) furan-2-carboxylate
State
State

At room temperature, (7-nitro-8-quinolyl) furan-2-carboxylate is generally a solid. It is stable under typical conditions.

Melting point (Celsius)
224.00
Melting point (Kelvin)
497.20
Boiling point (Celsius)
526.00
Boiling point (Kelvin)
799.20
General information
Molecular weight
336.27g/mol
Molar mass
336.2680g/mol
Density
1.4921g/cm3
Appearence

This compound typically appears as an orange to yellow crystalline solid.

Comment on solubility

Solubility of (7-nitro-8-quinolyl) furan-2-carboxylate

The solubility of (7-nitro-8-quinolyl) furan-2-carboxylate can be characterized by several factors that influence its behavior in various solvents. Overall, the solubility of this compound is primarily dictated by its molecular structure and functional groups:

  • Polarity: The presence of nitro (–NO2) groups enhances polarity, which can increase solubility in polar solvents such as water.
  • Hydrophobic regions: The quinolyl ring introduces hydrophobic character, potentially reducing solubility in highly polar solvents.
  • Solvent interactions: Solubility will vary significantly between different solvents (such as ethanol, acetone, or chloroform) due to unique interaction dynamics.
  • Temperature dependency: Generally, solubility increases with temperature; thus, this compound may have enhanced solubility in warm solvents.

As a summary, while (7-nitro-8-quinolyl) furan-2-carboxylate is predicted to exhibit moderate solubility in certain polar solvents due to its functional groups, exact solubility can only be definitively determined through experimental methods. Always consult experimental data for precise applications!

Interesting facts

Interesting Facts about (7-Nitro-8-quinolyl) furan-2-carboxylate

(7-Nitro-8-quinolyl) furan-2-carboxylate is a fascinating compound that exemplifies the intricate interplay between organic chemistry and medicinal applications. Its structure consists of a furan moiety combined with a quinoline derivative, which contributes to its unique chemical properties.

Key Features and Applications

  • Biological Activity: This compound has drawn attention for its potential biological activities, particularly in the realms of antimicrobial and antitumor research.
  • Fluorescent Properties: Due to its aromatic system, (7-nitro-8-quinolyl) furan-2-carboxylate exhibits notable fluorescent properties, making it useful in various imaging applications.
  • Potential as a Probe: Its ability to selectively bind to specific ions or biomolecules positions it as a possible candidate for use as a fluorescent probe in biological systems.

One of the most striking aspects of (7-nitro-8-quinolyl) furan-2-carboxylate is its structural diversity. The presence of both the nitrogen-containing ring and the furan ring makes this compound particularly intriguing for the synthesis of novel derivatives. Researchers often say, "The key to innovation in drug design lies within the diversity of chemical structures."

In summary, (7-nitro-8-quinolyl) furan-2-carboxylate is more than just a compound; it's a potential game-changer in drug discovery and biosensing technologies, making it a subject of ongoing research and interest in the scientific community.

Synonyms
BRN 1547144
2-FURANCARBOXYLIC ACID, 7-NITRO-8-QUINOLINYL ESTER
7-Nitro-8-quinolinyl 2-furancarboxylate
29007-34-9
DTXSID20183248
RefChem:261295
DTXCID30105739