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1-ethyl-2-[3-(1-ethylquinolin-1-ium-2-yl)prop-2-enylidene]quinoline

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Identification
Molecular formula
C27H22N+
CAS number
.123456789
IUPAC name
1-ethyl-2-[3-(1-ethylquinolin-1-ium-2-yl)prop-2-enylidene]quinoline
State
State

The compound is generally in a solid state at room temperature.

Melting point (Celsius)
236.00
Melting point (Kelvin)
509.15
Boiling point (Celsius)
484.00
Boiling point (Kelvin)
757.15
General information
Molecular weight
370.50g/mol
Molar mass
370.4950g/mol
Density
1.2010g/cm3
Appearence

The compound appears as a crystalline solid. It generally exhibits a yellow to orange color due to its extended conjugated system, which can lead to distinct light absorption properties.

Comment on solubility

Solubility of 1-ethyl-2-[3-(1-ethylquinolin-1-ium-2-yl)prop-2-enylidene]quinoline

The solubility of 1-ethyl-2-[3-(1-ethylquinolin-1-ium-2-yl)prop-2-enylidene]quinoline in various solvents can exhibit interesting characteristics due to its complex molecular structure. Generally, the solubility of this compound can be influenced by several factors:

  • Polarity of the Solvent: This compound may show higher solubility in polar solvents such as water or alcohol due to the presence of nitrogen atoms in its quinoline moiety.
  • Temperature Dependence: Increased temperature typically enhances solubility, which is crucial for applications involving reactions in solution.
  • Functional Groups: The presence of the quinolin-ium cation facilitates interactions with polar solvents, potentially increasing solubility.
  • pH Sensitivity: Being a nitrogen-containing compound, its ionization state can change with pH, affecting solubility.

While specific quantitative solubility data for this compound may not be readily available, it is essential to consider that solubility can vary widely based on the aforementioned factors. Thus, it's often observed that:

  1. "The right solvent can make a world of difference."
  2. Controlled solubility can lead to innovative applications in pharmaceuticals and materials science.

In conclusion, understanding the solubility profile of 1-ethyl-2-[3-(1-ethylquinolin-1-ium-2-yl)prop-2-enylidene]quinoline is critical for its effective utilization in both research and industrial applications.

Interesting facts

Interesting Facts about 1-Ethyl-2-[3-(1-ethylquinolin-1-ium-2-yl)prop-2-enylidene]quinoline

This fascinating compound belongs to a diverse class of organic molecules known for their intricate structures and biological activities. Here are some compelling insights into this unique compound:

  • Quinoline Derivative: This compound contains the quinoline moiety, which is well-known for its presence in various natural and synthetic compounds, many of which exhibit significant pharmacological properties.
  • Intricate Structure: The presence of multiple functional groups, such as the ethyl and prop-2-enylidene groups, contributes to the molecule's complexity and potentially impacts its chemical behavior and reactivity.
  • Potential in Medicinal Chemistry: Compounds harboring similar structural characteristics have been researched for their potential as anti-cancer, anti-inflammatory, and antimicrobial agents. Research into this compound may yield valuable insights into new therapeutic applications.
  • Dimensionality in Design: The unique arrangement of quinoline rings creates opportunities for designing molecules with specific orientations, which can enhance interactions with biological targets.
  • Research Opportunities: As a primarily synthetic compound, it offers avenues for investigations into synthetic methodologies, reaction mechanisms, and the exploration of analogous compounds to assess their biological efficacy.

"The beauty of organic chemistry lies in the infinite possibilities of structure and function, and this compound is a prime example."

As research progresses, the study of compounds like 1-ethyl-2-[3-(1-ethylquinolin-1-ium-2-yl)prop-2-enylidene]quinoline will enhance our understanding of chemistry and biology and may lead to breakthroughs in pharmaceutical development.

Synonyms
pinacyanol cation
20187-38-6
SCHEMBL2413213
DTXSID4048357
1,1'-Diethyl-2,2'-quinocarbocyanine
Q27123663