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No common name

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Identification
Molecular formula
C22H34Cl3N2S
CAS number
104973-11-5
IUPAC name
2-[(3-chloro-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinolin-5-ium-11-yl)sulfanyl]ethyl-diethyl-ammonium;dichloride
State
State

At room temperature, it is in a solid state with a crystalline structure. The compound is typically stable at ambient conditions, though it should be kept away from sources of moisture and direct sunlight to prevent degradation.

Melting point (Celsius)
143.00
Melting point (Kelvin)
416.15
Boiling point (Celsius)
213.00
Boiling point (Kelvin)
486.15
General information
Molecular weight
456.88g/mol
Molar mass
456.8820g/mol
Density
1.2342g/cm3
Appearence

This compound is a crystalline solid with no distinct color. It appears as off-white or pale yellow crystals, depending on the purity and the presence of any impurities.

Comment on solubility

Solubility of 2-[(3-chloro-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinolin-5-ium-11-yl)sulfanyl]ethyl-diethyl-ammonium;dichloride

The compound 2-[(3-chloro-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinolin-5-ium-11-yl)sulfanyl]ethyl-diethyl-ammonium;dichloride exhibits unique solubility characteristics that can be understood through several key factors:

  • Polarity: The presence of multiple polar groups, including ammonium and sulfanyl functionalities, contributes to its solubility in polar solvents.
  • Solvent Interaction: This compound is particularly soluble in water due to hydrogen bonding capabilities and ionic interactions with the solvent molecules.
  • Concentration Dependency: As with many ionic compounds, solubility may increase with temperature; thus, higher temperatures can enhance the dissolution process.
  • Electrolytic Nature: The dichloride part of the compound indicates that it will dissociate in solution, increasing the ionic strength and improving solubility in aqueous environments.

In practice, the solubility of this compound suggests that researchers and practitioners might utilize it effectively in aqueous solutions when exploring its chemical properties and potential applications. As one might summarize, "the more polar and ionic the substance, the more likely it is to dissolve in polar solvents."

Overall, understanding the solubility of this compound opens avenues for its use in various chemical processes and applications.

Interesting facts

Interesting Facts about 2-[(3-chloro-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinolin-5-ium-11-yl)sulfanyl]ethyl-diethyl-ammonium;dichloride

This intriguing compound belongs to a class of chemical substances with a very unique structure, characterized by its complex cyclic systems and nitrogen-containing groups. Here are several noteworthy aspects that make this compound fascinating:

  • Cyclic Structures: The presence of a cyclohepta[b]quinoline framework indicates that this compound features multiple interconnected rings, which contribute to its stability and reactivity.
  • Quaternary Ammonium Compound: As a quaternary ammonium salt, it demonstrates unique ionic properties, making it interesting for various biological applications.
  • Sulfanyl Group: The incorporation of a sulfanyl (-S-) group can enhance the compound's biological activity, potentially increasing its effectiveness in medicinal chemistry.
  • Antimicrobial Potential: Many compounds with similar structures have been studied for their antimicrobial properties, suggesting this compound may have similar beneficial effects.

The compound's structure and chemical attributes highlight its potential for research and development, particularly in the field of medicinal chemistry. Scientists often quote that "the most exciting discoveries often come from the exploration of complex molecular architectures," and this compound certainly embodies that philosophy.
To utilize this compound effectively, researchers need to consider the intricate interplay of its functional groups, which influence not only its properties but also its applications in various fields, including pharmacology and materials science. It remains an outstanding example of how complexity in chemistry can lead to remarkable innovation.

Synonyms
18833-71-1
6H-Cyclohepta(b)quinoline, 3-chloro-11-((2-(diethylamino)ethyl)thio)-7,8,9,10-tetrahydro-, dihydrochloride