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Naphtho[2,3-f]quinoline

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Identification
Molecular formula
C17H11N
CAS number
135-19-3
IUPAC name
naphtho[2,3-f]quinoline
State
State

At room temperature, Naphtho[2,3-f]quinoline is in a solid state, typically found as a powder.

Melting point (Celsius)
120.00
Melting point (Kelvin)
393.00
Boiling point (Celsius)
540.90
Boiling point (Kelvin)
814.00
General information
Molecular weight
229.28g/mol
Molar mass
229.2820g/mol
Density
1.3210g/cm3
Appearence

Naphtho[2,3-f]quinoline typically appears as a pale yellow powder. This aromatic compound is characterized by its fused ring structure, contributing to its vibrant hue. The powder may exhibit some slight color variations based on purity and particle size.

Comment on solubility

Solubility of naphtho[2,3-f]quinoline

Naphtho[2,3-f]quinoline is a unique organic compound that exhibits specific solubility characteristics. Generally, the solubility of this compound can be defined based on several key factors:

  • Polarity: Naphtho[2,3-f]quinoline has a relatively low polarity, which typically results in limited solubility in polar solvents such as water.
  • Solvent Compatibility: It is more soluble in non-polar organic solvents, such as:
    • Hexane
    • Chloroform
    • Toluene
  • Temperature Influence: Solubility can be affected by temperature, with increased temperatures often enhancing the solubility of organic compounds.
  • Functional Groups: The presence of substituents or functional groups can significantly alter the solubility profile. For instance, electron-donating or withdrawing groups can impact hydrogen bonding and overall interactions with solvents.

In summary, "naphtho[2,3-f]quinoline is sparingly soluble in water but shows favorable solubility in organic solvents." This solubility behavior is crucial for various applications, particularly in fields like organic synthesis and material science. Understanding the solubility of naphtho[2,3-f]quinoline can aid scientists in effectively utilizing this compound in their research.

Interesting facts

Interesting Facts about Naphtho[2,3-f]quinoline

Naphtho[2,3-f]quinoline is a fascinating compound that belongs to the family of quinolines, which are known for their complex aromatic structures. This particular naphthoquinoline has unique properties and is studied for several significant reasons:

  • Structure and Stability: The fused ring system of naphtho[2,3-f]quinoline contributes to its stability, making it an intriguing subject of study in organic chemistry.
  • Potential Applications: Due to its aromatic character, this compound may exhibit fluorescence, making it useful in various applications such as organic light-emitting diodes (OLEDs) and as fluorescent probes in biological systems.
  • Biological Relevance: Compounds in the quinoline family have been investigated for their biological activities. Naphtho[2,3-f]quinoline could potentially have applications in pharmacology, particularly in the development of antimalarial and anticancer agents.
  • Research Interest: Its unique electronic properties can influence the development of organic semiconductors and materials science, sparking interest among materials chemists.

“The study of such structurally fascinating compounds can reveal much about the intricacies of organic chemistry and materials science.”

In summary, naphtho[2,3-f]quinoline serves as a prime example of how intricate organic compounds can lead to advances in various scientific fields, from medicinal chemistry to materials science.

Synonyms
Naphtho[2,3-f]quinoline
beta-Anthraquinoline
1,2(N)-Pyridinoanthracene
4-Azabenz(a)anthracene
4'-Aza-1,2-benzanthracene
NAPHTHO(2,3-f)QUINOLINE
224-98-6
SFK1GL5XQL
NSC 400548
BRN 0154950
UNII-SFK1GL5XQL
NSC-400548
DTXSID40176930
4-Azabenz[a]anthracene
anthrapyridine
NSC400548
.beta.-Anthraquinoline
SCHEMBL379402
DTXCID2099421
WLN: T D6 B666 ONJ