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5-Benzyl-3-(2-ammonioethyl)sulfanyl-1H-indole chloride

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Identification
Molecular formula
C17H19ClN2S
CAS number
374060-34-9
IUPAC name
2-(5-benzylsulfanyl-1H-indol-3-yl)ethylammonium;chloride
State
State

At room temperature, this compound is typically in a solid state, specifically as a crystalline solid or powder.

Melting point (Celsius)
185.00
Melting point (Kelvin)
458.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
334.87g/mol
Molar mass
334.8700g/mol
Density
1.2800g/cm3
Appearence

This compound typically appears as an off-white to pale yellow powder or crystalline solid. It may appear slightly different depending on the method of preparation and purity.

Comment on solubility

Solubility of 2-(5-benzylsulfanyl-1H-indol-3-yl)ethylammonium;chloride

The solubility of a compound can often serve as a pivotal factor in determining its practical applications and behavior in various environments. In the case of 2-(5-benzylsulfanyl-1H-indol-3-yl)ethylammonium;chloride, several key points regarding its solubility can be considered:

  • Polarity: The presence of an ammonium group suggests potential for high solubility in polar solvents such as water.
  • Chloride Ion: The chloride anion is typically soluble in water, which can enhance the solubility of the compound.
  • Organic Solvents: The benzylsulfanyl group may impart additional solubility in certain organic solvents, allowing for versatility in different solvent systems.
  • pH Dependence: The solubility may also be influenced by the pH of the solution, where varying acidity or basicity could affect ionization states.

As noted, solubility can be a complex interplay of molecular structure and environmental conditions. Therefore, it is not solely dependent on one factor but rather an amalgamation of several contributing elements. Understanding the solubility can lead to better applications in drug formulation, biochemical interactions, and more.

In conclusion, while the exact solubility parameters may require experimental determination, the characteristics of 2-(5-benzylsulfanyl-1H-indol-3-yl)ethylammonium;chloride suggest promising potential for solubility in both aqueous and organic environments.

Interesting facts

Interesting Facts about 2-(5-benzylsulfanyl-1H-indol-3-yl)ethylammonium Chloride

This compound, known as 2-(5-benzylsulfanyl-1H-indol-3-yl)ethylammonium chloride, presents a unique structure that piques the interest of many chemists and scientists alike due to its intriguing features:

  • Biological Relevance: Compounds containing the indole structure are often linked to important biological activities. Indole derivatives have been shown to display a variety of pharmacological properties, making them valuable in medicinal chemistry.
  • Sulfanyl Group: The presence of the sulfanyl (-S-) group contributes to the reactivity of this compound, leading to potential applications in organic synthesis and as a biological probe.
  • Ammonium Ion: The quaternary ammonium feature might make this compound useful in drug formulation, as it can enhance solubility and biological uptake in various systems.
  • Versatile Applications: Due to its multifaceted structure, this compound may have potential uses in developing new drugs, agrochemicals, or even as a research tool in biochemical studies.

As a scientist, it's fascinating to consider how the combination of the indole and ammonium characteristics could lead to novel pathways in therapeutic interventions. Moreover, understanding how modifications in the chemical structure influence the biological activity can inspire future research directions.
In a world of chemical diversity, compounds like 2-(5-benzylsulfanyl-1H-indol-3-yl)ethylammonium chloride remind us of the intricate relationships between structure and function in chemistry.

Synonyms
5-Benzylthiotryptamine hydrochloride
INDOLE, 3-(2-AMINOETHYL)-5-BENZYLTHIO-, HYDROCHLORIDE
3373-15-7