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Naphtho[2,1-f]isoquinoline

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Identification
Molecular formula
C17H11N
CAS number
522-60-1
IUPAC name
naphtho[2,1-f]isoquinoline
State
State

At room temperature, Naphtho[2,1-f]isoquinoline is typically a solid. Its structure provides stability up to its respective melting and boiling points.

Melting point (Celsius)
108.00
Melting point (Kelvin)
381.15
Boiling point (Celsius)
476.00
Boiling point (Kelvin)
749.15
General information
Molecular weight
215.27g/mol
Molar mass
215.2630g/mol
Density
1.2360g/cm3
Appearence

Naphtho[2,1-f]isoquinoline typically appears as a colorless to pale yellow solid. Its crystalline structure can sometimes impart a slightly lustrous finish.

Comment on solubility

Solubility Characteristics of Naphtho[2,1-f]isoquinoline

Naphtho[2,1-f]isoquinoline, a polycyclic aromatic compound, exhibits unique solubility behavior that is influenced by its structural properties. Here are some key points regarding its solubility:

  • Solvent Compatibility: This compound is generally insoluble in water due to its nonpolar aromatic nature. It shows a higher affinity for nonpolar solvents.
  • Solubility in Organic Solvents: Naphtho[2,1-f]isoquinoline is soluble in a variety of organic solvents such as:
    • Chloroform
    • Benzene
    • Toluene
  • Temperature Effects: As with many organic compounds, its solubility may increase with temperature, making heating a potential method to enhance dissolution in organic solvents.
  • Applications and Implications: Understanding the solubility profile is crucial for its use in various chemical applications, including:
    • Organic synthesis
    • Pharmaceutical formulations
    • Materials science

In conclusion, while naphtho[2,1-f]isoquinoline demonstrates significant solubility in nonpolar organic solvents, it remains largely insoluble in polar solvents like water. This solubility behavior is essential to consider for effective application and handling in laboratory settings.

Interesting facts

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

Naphtho[2,1-f]isoquinoline is a fascinating organic compound that belongs to a class of polycyclic aromatic hydrocarbons. Here are some intriguing highlights about this compound:

  • Structure and Formation: This compound features a unique fused ring structure that combines elements of naphthalene and isoquinoline. The specific arrangement of these rings contributes to its interesting chemical properties.
  • Potential Applications: Naphtho[2,1-f]isoquinoline is of interest in medicinal chemistry, particularly for its potential *antitumor* and *antiviral* activities. Research is ongoing to explore its therapeutic benefits in various contexts.
  • Reactivity: The presence of multiple aromatic rings makes this compound a versatile building block in organic synthesis. It can undergo various reactions, including electrophilic aromatic substitution, making it valuable in materials science.
  • Research Focus: Scientists are currently investigating its electronic properties and how they may differ from related structures. Such investigations are crucial for developing new materials in electronics and photonics.

The beauty of compounds like naphtho[2,1-f]isoquinoline lies in their complexity and the possibilities they represent for future discoveries. As researchers continue to unlock the secrets of these molecules, they open doors to innovations that could have lasting impacts in fields ranging from healthcare to materials engineering.

In the words of chemists, *“Every compound tells a story; it’s up to us to decipher it.”* Continue exploring the world of organic chemistry, and you may just uncover the next big breakthrough!

Synonyms
2-Azachrysene
Naphth(2,1-f)isoquinoline
3K6PRD9P0K
CCRIS 1605
218-02-0
UNII-3K6PRD9P0K
NSC 117035
NSC-117035
Naphth[2,1-f]isoquinoline
BRN 0154998
DTXSID60176210
4-20-00-04295 (Beilstein Handbook Reference)
NSC117035
SCHEMBL2930993
DTXCID1098701