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Tryptamine derivative

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Identification
Molecular formula
C14H19ClN2
CAS number
37415-66-6
IUPAC name
3-(5-ethylpyrrolidin-1-ium-2-yl)-1H-indole;chloride
State
State

At room temperature, this compound is typically found as a solid. It is generally stable if kept dry and stored properly.

Melting point (Celsius)
194.30
Melting point (Kelvin)
467.45
Boiling point (Celsius)
355.50
Boiling point (Kelvin)
628.65
General information
Molecular weight
282.82g/mol
Molar mass
282.8190g/mol
Density
1.2400g/cm3
Appearence

This compound appears as an off-white to pale yellow crystalline solid. The exact coloration can vary depending on the purity and specific conditions. It usually has a granular to powdered texture.

Comment on solubility

Solubility of 3-(5-ethylpyrrolidin-1-ium-2-yl)-1H-indole;chloride

The solubility of 3-(5-ethylpyrrolidin-1-ium-2-yl)-1H-indole;chloride is influenced by its ionic nature due to the presence of the chloride ion and the pyrrolidin-1-ium moiety. This compound, like many ammonium salts, tends to exhibit good solubility in polar solvents. Here are some key points regarding its solubility characteristics:

  • Polar Solvents: The compound is highly soluble in water and alcohols, owing to the ionic interactions and the hydrogen bonding capability of water.
  • Non-polar Solvents: In contrast, it displays poor solubility in non-polar solvents such as hexane or benzene, where ionic compounds generally struggle to dissolve.
  • pH Sensitivity: The solubility may also vary with pH, as changes in the protonation state can influence the overall charge and, subsequently, the solubility of the compound.

In summary, the solubility profile of this compound is primarily robust in polar environments but limited in non-polar conditions. Always consider the solvent effects and potential temperature influences when dissolving this compound for practical applications.

Interesting facts

Interesting Facts about 3-(5-ethylpyrrolidin-1-ium-2-yl)-1H-indole;chloride

The compound 3-(5-ethylpyrrolidin-1-ium-2-yl)-1H-indole;chloride, often referred to simply as indole-based ionic liquid, presents a fascinating case for study in the field of organic chemistry. Its structure combines the intriguing qualities of both indole—a well-known component in many biological systems—and pyrrolidine, contributing to its unique properties. Here are some compelling points to consider:

  • Versatile Applications: This compound's unique structure allows it to function as a versatile intermediate in various synthetic processes, including pharmaceuticals and agrochemicals.
  • Biological Interest: Indole derivatives are often associated with numerous biological activities, making this compound a potential candidate for drug discovery and development.
  • Stability and Solubility: The ionic nature of the compound suggests interesting solubility characteristics, as it may exhibit both ionic and non-ionic interactions in solution.
  • Electrochemical Properties: Due to its ionic nature, the compound is anticipated to have significant electrochemical properties, which can be harnessed in energy storage technologies.
  • Research Potential: The compound has garnered attention in research studies dedicated to understanding its role in organic electronics, where it may serve as a component in organic photovoltaics or organic field-effect transistors (OFETs).

As a student or a researcher, diving into the characteristics of 3-(5-ethylpyrrolidin-1-ium-2-yl)-1H-indole;chloride can expand your understanding of both synthetic methods and the diverse applications of indole derivatives. This compound not only highlights the complexity of chemical synthesis but also illustrates the interconnectedness of organic chemistry with real-world applications.

Synonyms
3-(5-Ethyl-2-pyrrolidinyl)indole hydrochloride
19137-74-7
INDOLE, 3-(5-ETHYL-2-PYRROLIDINYL)-, HYDROCHLORIDE