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Naphthoquinoline

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Identification
Molecular formula
C16H11N
CAS number
841-97-8
IUPAC name
naphtho[2,3-h]quinoline
State
State

At room temperature, naphthoquinoline is a solid. It maintains a crystalline structure which is common among many polycyclic aromatic compounds. The solid state allows for its practical uses in laboratories and industrial applications.

Melting point (Celsius)
139.00
Melting point (Kelvin)
412.15
Boiling point (Celsius)
403.00
Boiling point (Kelvin)
676.15
General information
Molecular weight
229.27g/mol
Molar mass
229.2720g/mol
Density
1.2400g/cm3
Appearence

Naphthoquinoline is a solid compound that typically appears as a yellowish crystalline powder. It retains the structural characteristics of both naphthalene and quinoline, giving it a distinct aromatic odor.

Comment on solubility

Solubility of Naphtho[2,3-h]quinoline

Naphtho[2,3-h]quinoline, a polycyclic aromatic compound, exhibits unique solubility characteristics that are important to its chemical behavior and applications. Understanding its solubility is crucial for various fields, including organic chemistry and materials science. Here are some key aspects:

  • Solvent Interaction: Naphtho[2,3-h]quinoline is generally soluble in organic solvents such as ethanol, acetone, and chloroform, due to its hydrophobic nature.
  • Water Solubility: This compound has poor solubility in water, which is typical for many polycyclic aromatic hydrocarbons.
  • Temperature Dependence: Solubility can also be affected by temperature, with higher temperatures typically increasing solubility in organic solvents.
  • Applications: Its solubility properties make it suitable for applications in organic synthesis and in the development of organic electronic materials.

In conclusion, the solubility of naphtho[2,3-h]quinoline reflects its non-polar character, necessitating the use of suitable organic solvents for effective dissolution. Understanding these properties is essential for manipulating this compound in various scientific pursuits.

Interesting facts

Interesting Facts About Naphtho[2,3-h]quinoline

Naphtho[2,3-h]quinoline is a fascinating compound that falls under the category of heterocycles, specifically aromatic compounds. Here are some intriguing aspects of this compound:

  • Aromatic Structure: The compound’s unique structure comprises fused rings, which contributes to its stability and distinct chemical properties.
  • Biological Significance: Naphtho[2,3-h]quinoline derivatives have been studied for their potential pharmacological activities. They exhibit various biological effects, making them candidates for research in medicinal chemistry.
  • Photophysical Properties: Many quinoline compounds, including naphtho[2,3-h]quinoline, exhibit interesting photophysical properties that can be utilized in developing organic electronic materials, fluorescent probes, and dyes.
  • Research Applications: The compound serves as a structural framework in organic synthesis and can also be utilized in the development of materials for organic light-emitting diodes (OLEDs) and photovoltaic cells.

As a **chemistry enthusiast**, one can delve into the diverse applications and implications of naphtho[2,3-h]quinoline. Here are a couple of notable quotes to consider:

"The beauty of chemistry lies in the relationships we forge with compounds and their reactions." - Anonymous
"Every chemical reaction is a step towards understanding the universe." - Anonymous

In conclusion, naphtho[2,3-h]quinoline embodies a composite of stability, biological relevance, and innovative applications, making it a compound worth exploring further in both academic and practical contexts.

Synonyms
1-Azabenz(a)anthracene
naphtho[2,3-h]quinoline
Naphtho(2,3-h)quinoline
84-56-0
CCRIS 1607
BRN 0155002
1-AZABENZ[A]ANTHRACENE
DTXSID40232888
1-Azabenzo[a]anthracene
AEQ2MZ5K5V
AZABENZ(A)ANTHRACENE
SCHEMBL5821259
DTXCID70155379