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(7-nitro-8-quinolyl) 4-phenylbenzoate

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Identification
Molecular formula
C22H14N2O4
CAS number
87386-72-5
IUPAC name
(7-nitro-8-quinolyl) 4-phenylbenzoate
State
State

Solid at room temperature. It generally exists in a stable form under standard conditions but should be stored in a cool, dry place away from light and moisture to prevent degradation.

Melting point (Celsius)
184.00
Melting point (Kelvin)
457.15
Boiling point (Celsius)
310.00
Boiling point (Kelvin)
583.15
General information
Molecular weight
348.36g/mol
Molar mass
348.3560g/mol
Density
1.3600g/cm3
Appearence

(7-nitro-8-quinolyl) 4-phenylbenzoate generally appears as a crystalline solid. The crystals are typically pale yellow to light yellow, owing to the presence of the nitro and quinolyl groups which can impart such coloration due to their aromatic and electron-withdrawing nature, respectively.

Comment on solubility

Solubility of (7-nitro-8-quinolyl) 4-phenylbenzoate

The solubility of (7-nitro-8-quinolyl) 4-phenylbenzoate can be influenced by several factors due to its complex molecular structure. Here are some insights regarding its solubility characteristics:

  • Solvent Compatibility: This compound exhibits varying solubility in organic solvents, particularly in non-polar and moderately polar environments. It is likely to be soluble in solvents such as ethanol, methanol, and dichloromethane.
  • Water Solubility: The compound's solubility in water is expected to be very low. This is typical for many organic compounds that lack sufficient polar functional groups to interact favorably with water molecules.
  • Temperature Influence: As with many organic compounds, an increase in temperature may enhance solubility, allowing for greater dissolution rates in organic solvents.
  • pH Sensitivity: Changes in pH can affect the solubility of (7-nitro-8-quinolyl) 4-phenylbenzoate, especially if ionization occurs at different pH levels, thus impacting its interaction with solvents.

Overall, it is crucial to evaluate the specific solvent environment, as the physical and chemical nature of this compound can greatly influence its solubility behavior. As such, "understanding solubility is just as important as knowing the structure" for practical applications in various fields, including pharmaceuticals and materials science.

Interesting facts

Interesting Facts about (7-nitro-8-quinolyl) 4-phenylbenzoate

(7-nitro-8-quinolyl) 4-phenylbenzoate is a fascinating compound that has intrigued chemists and researchers alike due to its unique structure and properties. Here are some key points that make this compound particularly interesting:

  • Dual Functionality: The presence of both a quinoline and benzoate moiety suggests a versatility in chemical reactivity, allowing it to participate in a variety of reactions.
  • Fluorescent Properties: Compounds similar to this structure often exhibit fluorescence, making them useful in photochemical applications, including fluorescence microscopy and solar energy conversion.
  • Biological Relevance: Quinoline derivatives are known for their biological activities. They can act as antimicrobial, antiviral, and anticancer agents, sparking interest in medicinal chemistry.
  • Research Applications: Due to its structural characteristics, this compound is often utilized in research concerning organic synthesis and material chemistry, potentially leading to new discoveries.
  • Recent Studies: Recent literature has shown that derivatives of quinoline such as this one can act as effective ligands in coordination chemistry, forming complexes with various metal ions.

The property of selectivity in reactions involving quinolines has paved the way for the development of new methodologies in organic synthesis, enabling the formation of complex molecular architectures with high yields. Researchers are excited about exploring the myriad applications of (7-nitro-8-quinolyl) 4-phenylbenzoate, further expanding its role in both practical and theoretical chemistry.

In conclusion, the structure and functional capabilities of (7-nitro-8-quinolyl) 4-phenylbenzoate make it a compound worth studying, combining aesthetics with scientific significance. Whether used in laboratories for practical applications or as a model for understanding complex chemical phenomena, its impact is undeniable.

Synonyms
BRN 1552521
29002-03-7
4-BIPHENYLCARBOXYLIC ACID, 7-NITRO-8-QUINOLYL ESTER
7-Nitro-8-quinolyl 4-biphenylcarboxylate
8-Quinolinol, 7-nitro-, 4-biphenylcarboxylate
DTXSID30183198
RefChem:290382
DTXCID40105689
SCHEMBL4459176
4-BIPHENYLCARBOXYLIC ACID,7-NITRO-8-QUINOLYL ESTER