Tryptamine hydrochloride
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- Molecular formula
- C11H15ClN2
- CAS Number
- 72-04-8
- IUPAC Name
- 3-(1,4-dimethylpyrrolidin-1-ium-2-yl)-1H-indole;chloride
- Molecular Weight
- 218.71g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1100g/cm3
- Synonyms
- 3-(1, 4-Dimethyl-2-pyrrolidinyl)indole hydrochloride
Identification
Interesting facts
Interesting Facts About 3-(1,4-Dimethylpyrrolidin-1-ium-2-yl)-1H-indole; Chloride
The compound 3-(1,4-dimethylpyrrolidin-1-ium-2-yl)-1H-indole; chloride is a fascinating example of how organic chemistry blends complexity and functionality. Here are some interesting aspects:
- Structural Diversity: The presence of both the pyrrolidine and indole moieties enhances the structural diversity of this compound. This unique combination leads to numerous potential biological activities and applications in medicinal chemistry.
- Biological Relevance: Indole derivatives are widely recognized for their bioactivity, including roles in neurotransmission and as building blocks for many natural products. Thus, compounds like this one may hold potential in pharmaceuticals aimed at treating neurological disorders.
- Ionic Relationship: The chloride ion plays a crucial role in solubility and reactivity. As a counterion, it can significantly influence the molecular interactions and biological effectiveness of the compound.
- Research Potential: There is an increasing interest in synthesizing and studying similar compounds for their potential as ion channel modulators. This could lead to advances in the development of drugs targeting specific receptors.
- Synthesizing Challenges: The synthesis of complex organic molecules like 3-(1,4-dimethylpyrrolidin-1-ium-2-yl)-1H-indole; chloride often poses challenges, making it a compelling subject for developing new synthetic methodologies in organic chemistry.
In summary, 3-(1,4-dimethylpyrrolidin-1-ium-2-yl)-1H-indole; chloride serves as an intriguing subject for scientists looking to explore the intersections of structure, reactivity, and biological function. Its role in expanding the library of bioactive compounds only emphasizes the importance of continued research in this area.