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Naphtho[2,3-h]isoquinoline

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Identification
Molecular formula
C19H13N
CAS number
57736-11-7
IUPAC name
naphtho[2,3-h]isoquinoline
State
State

At room temperature, Naphtho[2,3-h]isoquinoline is a solid. It is typically encountered as a crystalline powder that may form larger crystals under specific conditions.

Melting point (Celsius)
105.00
Melting point (Kelvin)
378.00
Boiling point (Celsius)
680.00
Boiling point (Kelvin)
953.00
General information
Molecular weight
253.32g/mol
Molar mass
253.3030g/mol
Density
1.4000g/cm3
Appearence

Naphtho[2,3-h]isoquinoline is a polycyclic aromatic compound that typically appears as a colorless to pale yellow crystalline solid. The compound's unique structure, consisting of fused aromatic rings, contributes to its distinct crystallinity and potential for bright coloration when well-formed crystals are observed.

Comment on solubility

Solubility of Naphtho[2,3-h]isoquinoline

Naphtho[2,3-h]isoquinoline, denoted chemically as C13H9N, exhibits unique solubility characteristics that are worth noting. This organic compound belongs to a class of fused polycyclic systems, which influences its interactions with solvents.

Here are some key points regarding its solubility:

  • Low Solubility in Water: Naphtho[2,3-h]isoquinoline is generally insoluble in water, due to its hydrophobic nature and structure, which tends to resist dissolution in polar solvents.
  • Solubility in Organic Solvents: This compound shows better solubility in a variety of organic solvents such as:
    1. Chloroform
    2. Toluene
    3. Dichloromethane
    4. Acetone
    5. Ethyl acetate
  • Factors Influencing Solubility: The solubility can be influenced by factors such as:
    1. Temperature: Higher temperatures often result in increased solubility of organic compounds.
    2. Presence of co-solvents: Combining solvents can enhance solubility.

In summary, while Naphtho[2,3-h]isoquinoline is relatively insoluble in water, it finds better compatibility with non-polar and moderately polar organic solvents, highlighting the importance of solvent choice when working with this compound.

Interesting facts

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

Naphtho[2,3-h]isoquinoline is a fascinating compound that piques the interest of scientists and researchers alike due to its unique structure and potential applications in various fields. Here are some intriguing aspects of this compound:

  • Structural Complexity: The compound features a fused ring system that combines the naphthalene and isoquinoline structures. This complex architecture contributes to its interesting electronic properties.
  • Biological Significance: Research has indicated that naphtho[2,3-h]isoquinoline and its derivatives exhibit biological activities. They can function as potential leads for drug development in medicinal chemistry.
  • Fluorescence Properties: Some derivatives of naphtho[2,3-h]isoquinoline display significant fluorescence, making them useful in the fields of materials science and optics, particularly in the design of organic light-emitting diodes (OLEDs).
  • Synthetic Routes: The synthesis of naphtho[2,3-h]isoquinoline can be achieved through various methods, including cyclization reactions that showcase its versatility in organic synthesis.
  • Applications in Chemistry: This compound serves as a valuable building block for synthesizing more complex organic molecules, which can lead to the exploration of new pharmaceuticals and functional materials.

In summary, naphtho[2,3-h]isoquinoline is not just a fascinating molecule due to its structure but also holds promise in medicinal and material sciences. Continued research in this area could unveil new discoveries and applications, making it a rich topic for exploration in chemistry.

Synonyms
NAPHTH(2,3-h)ISOQUINOLINE
2-Azabenz(a)anthracene
CCRIS 1599
25082-33-1
BRN 4413709
2-Azabenz[a]anthracene
DTXSID50179775
Naphth[2,3-h]isoquinoline
RefChem:365229
DTXCID10102266