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Naphtho[1,2-h]quinoline

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Identification
Molecular formula
C15H9N
CAS number
273-03-0
IUPAC name
naphtho[1,2-h]quinoline
State
State

At room temperature, Naphtho[1,2-h]quinoline exists in a solid state. The compound's aromatic nature contributes to its stable solid form. It does not volatilize easily, which is typical of larger aromatic compounds with extended conjugated systems.

Melting point (Celsius)
126.00
Melting point (Kelvin)
399.15
Boiling point (Celsius)
470.00
Boiling point (Kelvin)
743.15
General information
Molecular weight
217.27g/mol
Molar mass
217.2670g/mol
Density
1.3640g/cm3
Appearence

Naphtho[1,2-h]quinoline appears as a crystalline solid. These crystals can range from pale yellow to a brownish color, depending on the purity and specific batch of the compound. Its appearance is typical of many aromatic heterocyclic compounds, where intermolecular forces lead to the formation of crystalline structures.

Comment on solubility

Solubility of Naphtho[1,2-h]quinoline

Naphtho[1,2-h]quinoline, a polycyclic aromatic compound, demonstrates unique solubility characteristics that can significantly influence its behavior in different environments. Understanding its solubility is essential for applications in organic chemistry and material science. Here are some key points regarding the solubility of this compound:

  • Polar Solvents: Naphtho[1,2-h]quinoline exhibits limited solubility in polar solvents such as water due to its hydrophobic nature. Its complex aromatic structure tends to repel polar molecules.
  • Non-Polar Solvents: Conversely, it shows a higher solubility in non-polar solvents (e.g., hexane, toluene), making it suitable for processes requiring organic solvents.
  • Temperature Dependence: Like many organic compounds, its solubility can be affected by temperature changes, generally increasing as the temperature rises.
  • Concentration Limits: High concentrations can lead to saturation, where no further dissolution occurs, often resulting in precipitate formation.

As a result, when working with naphtho[1,2-h]quinoline, it is crucial to select the appropriate solvent to ensure optimal solubility and reactivity. Understanding these solubility dynamics can greatly enhance the effectiveness of your chemical applications.

Interesting facts

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

Naphtho[1,2-h]quinoline is a fascinating aromatic heterocycle with a rich history in both synthetic chemistry and organic materials. This compound belongs to the family of quinolines, which are known for their wide array of applications. Here are some intriguing insights into this compound:

  • Diverse Applications: Naphtho[1,2-h]quinoline finds its use in various fields, such as pharmaceuticals, agrochemicals, and material science, demonstrating its versatility.
  • Fluorescent Properties: Due to its unique structure, this compound exhibits interesting photophysical properties, making it a candidate for use in optical devices and fluorescent dyes.
  • Biological Significance: Some derivatives of naphtho[1,2-h]quinoline are known to have antimicrobial and anticancer properties, which makes it an area of interest for drug discovery.
  • Synthesis Challenges: The synthesis of naphtho[1,2-h]quinoline can present challenges due to the need for precise conditions to avoid undesired side reactions, making it a subject of study for organic chemists.

As the fields of chemistry and material science evolve, naphtho[1,2-h]quinoline continues to capture the attention of researchers worldwide. Its unique properties and potential applications ensure that it remains a vital compound for future studies.

Synonyms
4-Azachrysene
NAPHTHO(1,2-h)QUINOLINE
218-19-9
CCRIS 1606
Naphthochinolin
BRN 0154997
SCHEMBL686683
DTXSID80176212