Interesting facts
Interesting Facts about 2-(5-chloro-1H-indol-3-yl)-2-methyl-propan-1-amine
2-(5-chloro-1H-indol-3-yl)-2-methyl-propan-1-amine, often referred to simply as a chloroindole derivative, belongs to a fascinating class of compounds characterized by their structural complexity and biological significance. Here are some intriguing aspects of this compound:
- Structural Versatility: The presence of both an indole ring and an amine group in the structure makes this compound a key player in medicinal chemistry, potentially serving as a scaffold for drug development.
- Biological Activity: Compounds with indole derivatives have been studied for various pharmacological properties, including their role in antidepressant, anti-inflammatory, and anticancer activities.
- Synthetic Pathways: The synthesis of chloroindole derivatives like this one is a significant topic in organic chemistry. The synthesis often involves methods such as coupling reactions and functional group modifications, providing a rich area for research and experimentation.
- Environmental Significance: Indole and its derivatives often show up in natural products and biological systems, serving as precursors to a range of essential biological compounds, including hormones and neurotransmitters.
- Research Investigations: Scientists are continually exploring the potential applications of compounds like 2-(5-chloro-1H-indol-3-yl)-2-methyl-propan-1-amine in the treatment of various diseases, making it a hot topic in current scientific literature.
In summary, the exploration of 2-(5-chloro-1H-indol-3-yl)-2-methyl-propan-1-amine not only highlights the intricate connections between structure and function in chemistry but also emphasizes the ongoing quest for novel therapeutic agents. As a **scientist** or **chemistry student**, delving into the properties and applications of such compounds can lead to significant discoveries and innovations.
Synonyms
BRN 0397126
14487-95-7
5-Chloro-beta,beta-dimethyltryptamine
INDOLE, 5-CHLORO-3-(2-AMINO-1,1-DIMETHYLETHYL)-
DTXSID90162828
DTXCID6085319
5-22-10-00185 (Beilstein Handbook Reference)
SCHEMBL9268928
QDTMEDNJIZALMQ-UHFFFAOYSA-N
[1-(5-chloro-1H-indol-3-yl)-1,1-dimethylethyl]amine
Solubility of 2-(5-chloro-1H-indol-3-yl)-2-methyl-propan-1-amine
The solubility of 2-(5-chloro-1H-indol-3-yl)-2-methyl-propan-1-amine can vary significantly depending on the solvent and environmental conditions. This compound, also referred to as a substituted indole derivative, presents unique solubility characteristics:
It is crucial to note that the specific conditions (like pH and presence of other solutes) can greatly impact solubility. As stated, "The beauty of chemistry lies in its complexities"—every compound has a unique behavior in different environments.
In practice, conducting solubility tests in various solvents can give a clearer picture of how 2-(5-chloro-1H-indol-3-yl)-2-methyl-propan-1-amine behaves, thus informing its application in pharmaceuticals and research.