5-Benzyl-3-(2-ammonioethyl)sulfanyl-1H-indole chloride
- Molecular formula
- C17H19ClN2S
- CAS Number
- 374060-34-9
- IUPAC Name
- 2-(5-benzylsulfanyl-1H-indol-3-yl)ethylammonium;chloride
- Molecular Weight
- 334.87g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2800g/cm3
- Synonyms
- 5-Benzylthiotryptamine hydrochloride
Identification
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.