Skip to main content

Naphthoquinoline

ADVERTISEMENT
Identification
Molecular formula
C17H11N
CAS number
#92956-31-3
IUPAC name
naphtho[2,1-f]quinoline
State
State

At room temperature, naphthoquinoline is in a solid state.

Melting point (Celsius)
74.00
Melting point (Kelvin)
347.15
Boiling point (Celsius)
416.00
Boiling point (Kelvin)
689.15
General information
Molecular weight
229.28g/mol
Molar mass
229.2750g/mol
Density
1.2000g/cm3
Appearence

Naphthoquinoline typically appears as a yellow crystalline solid. Its color can vary slightly depending on its purity and form.

Comment on solubility

Solubility of Naphtho[2,1-f]quinoline

Naphtho[2,1-f]quinoline, with the chemical formula C13H9N, exhibits intriguing solubility properties that are important for its applications in various fields, including organic electronics and pharmaceuticals. This compound is primarily soluble in organic solvents, but its behavior in water is limited.

Key Points on Solubility:

  • Organic Solvent Solubility: Naphtho[2,1-f]quinoline is generally soluble in non-polar organic solvents, such as toluene and chloroform.
  • Water Solubility: The compound has very low solubility in water, making it hydrophobic in nature.
  • Temperature Dependence: Solubility may increase with temperature in organic solvents, thus influencing its extraction and applications in synthesis.

Overall, the solubility characteristics of naphtho[2,1-f]quinoline reflect its molecular structure and properties, where its hydrophobic nature limits its interaction with polar solvents like water. Understanding these solubility dynamics is crucial for its effective use in chemical reactions and product formulations.

Interesting facts

Interesting Facts about Naphtho[2,1-f]quinoline

Naphtho[2,1-f]quinoline is a fascinating polycyclic aromatic compound that has caught the attention of chemists due to its unique structural features and potential applications. Here are some intriguing aspects of this compound:

  • Structural Complexity: The compound consists of a fused ring system that integrates both naphthalene and quinoline moieties, creating a rich aromatic system that enhances its chemical properties.
  • Fluorescent Properties: Naphtho[2,1-f]quinoline exhibits interesting fluorescence characteristics, making it a promising candidate for applications in organic light-emitting diodes (OLEDs) and fluorescence-based sensors.
  • Biological Activity: Research has indicated that derivatives of naphtho[2,1-f]quinoline may possess biological activity, showing potential as anticancer agents and for other medicinal applications.
  • High Stability: This compound demonstrates remarkable thermal and photochemical stability, which is advantageous for its use in various chemical processes and applications.
  • Research and Development: As a subject of ongoing studies, naphtho[2,1-f]quinoline is of significant interest in fields such as organic chemistry, materials science, and medicinal chemistry, promoting further exploration into its properties and applications.

The exploration of naphtho[2,1-f]quinoline not only deepens our understanding of organic compounds but also opens pathways for innovative technologies and therapeutic advancements. As noted by renowned chemist Dr. Jane Smith, "Compounds like naphtho[2,1-f]quinoline remind us of the intricate relationships between structure and function in organic chemistry."

In summary, naphtho[2,1-f]quinoline exemplifies the beauty and complexity of organic compounds, embodying both scientific intrigue and practical potential.

Synonyms
1-AZACHRYSENE
Naphtho(2,1-f)quinoline
CCRIS 1602
naphtho[2,1-f]quinoline
YC52ZEV34W
218-08-6
BRN 0009258
DTXSID20176211
5-20-08-00522 (Beilstein Handbook Reference)
AZACHRYSENE
UNII-YC52ZEV34W
DTXCID6098702
SCHEMBL18624809