Interesting facts
Interesting Facts about 2-(1-methylindol-3-yl)ethanamine
2-(1-methylindol-3-yl)ethanamine, commonly referred to as Indoleethylamine, is a fascinating compound with intriguing characteristics and applications:
- Structural Significance: This compound features an indole ring, which is known for its presence in many biologically active compounds and natural products. The indole structure is believed to contribute to the molecule's unique chemical properties.
- Biological Relevance: Indole derivatives, including this compound, are often studied in relation to their roles in neurotransmission. They are thought to interact with various receptors in the brain, making them of interest in neurochemical research.
- Synthesis Pathways: The synthesis of 2-(1-methylindol-3-yl)ethanamine can involve multi-step chemical reactions, typically incorporating indole derivatives, amines, and various reagents. Exploring these methods can enhance one’s understanding of synthetic organic chemistry.
- Potential Applications: Given its structural framework, 2-(1-methylindol-3-yl)ethanamine may have applications in pharmacology, potentially serving as a template for developing new medications associated with mood disorders and psychoactive effects.
- Research Opportunities: This compound opens up a myriad of research avenues, particularly in the fields of medicinal chemistry, pharmacology, and neurochemistry. Scientists continue to investigate its properties, effects, and potential therapeutic uses.
In conclusion, 2-(1-methylindol-3-yl)ethanamine stands as a compelling subject for anyone fascinated by the intersection of chemistry and biology. Its structural elegance and potential impacts in neuroscience make it a noteworthy compound in modern chemical research.
Synonyms
7518-21-0
1-METHYLTRYPTAMINE
1-Methyl-1H-indole-3-ethylamine
EINECS 231-377-1
231-377-1
2-(1-methyl-1H-indol-3-yl)ethanamine
2-(1-methylindol-3-yl)ethanamine
1H-Indole-3-ethanamine,1-methyl-
2-(1-METHYL-1H-INDOL-3-YL)ETHAN-1-AMINE
3-(2-AMINOETHYL)-1-METHYLINDOLE
CHEMBL3330641
1-Methyltryptamine, free base
N-Methylisotryptamine
a-methyltryptamine
1H-Indole-2-ethanamine, 1-methyl-
BRN 0473426
Tryptamine, 1-methyl-
N-?-METHYLTRYPTAMINE
Oprea1_757922
SCHEMBL332959
DTXSID80991164
CHEBI:125627
2-(1-methyl-3-indolyl)ethanamine
BBL036339
BDBM50025215
MFCD00057093
STK367793
VT1228
AKOS000276207
FM52291
MB00487
1-Methyltryptamine, >=95.0% (GC)
1-METHYL-1H-INDOLE-3-ETHANAMINE
2-(1-methyl-1H-indol-3-yl)ethylamine
2-(1-methyl-1H-indol-3-yl)-ethylamine
AS-54752
NS00047653
EN300-139143
M-4645
5-22-10-00042 (Beilstein Handbook Reference)
AE-848/30742009
2-(1-METHYL-1H-INDOL-3-YL)-1-ETHANAMINE
BRD-K74773935-001-01-6
Q27216239
F2106-0181
55FC1B01-ABF5-490D-A277-3CF781E25C03
1ES
Solubility of 2-(1-methylindol-3-yl)ethanamine
The solubility of 2-(1-methylindol-3-yl)ethanamine in various solvents is an essential aspect to consider in both laboratory and practical applications. This compound is a substituted amine with an indole moiety, which significantly influences its solubility properties. Here are some key points regarding its solubility:
In summary, the solubility of 2-(1-methylindol-3-yl)ethanamine is quite interactive and depends on multiple factors, which makes it essential to consider the choice of solvent in practical applications.
Understanding these solubility properties can lead to improved handling and utilization of this compound in various chemical processes.