Interesting facts
Interesting Facts about N,N-Diethyl-2-(1H-Indol-3-yl)ethanamine
N,N-Diethyl-2-(1H-indol-3-yl)ethanamine, commonly known as a derivative of indole, is a fascinating compound that has garnered attention in both the fields of organic chemistry and pharmacology. Here are some noteworthy facts about this intriguing molecule:
- Structure and Function: This compound features an indole moiety, which is a bicyclic structure that comprises a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. Indole derivatives are important in medicinal chemistry due to their structural similarity with various neurotransmitters.
- Biological Activity: Compounds in this class are often studied for their potential pharmacological effects. Research shows that they may exhibit psychoactive properties, contributing to their investigation in the context of neurological disorders and mental health treatments.
- Applications in Research: Scientists are exploring N,N-diethyl-2-(1H-indol-3-yl)ethanamine for its potential as a tool in investigating the serotonin receptors. These receptors play a critical role in regulating mood, anxiety, and cognitive functions.
- Synthetic Routes: The synthesis of this compound can involve a series of chemical reactions, including alkylation and amination. The methods for its synthesis often emphasize the need for precision to achieve high purity and desired yields.
- Historical Significance: Indole derivatives have played a significant role in the discovery of various therapeutic agents, including antidepressants and anxiolytics, marking a historical connection between organic chemistry and modern medicine.
In summary, N,N-diethyl-2-(1H-indol-3-yl)ethanamine stands out not only for its unique structure and biological relevance but also for its potential implications in the broader fields of pharmacology and neuroscience. As research continues to unveil new properties and applications, this compound remains a subject of great interest for chemists and medical researchers alike.
Synonyms
N,N-Diethyltryptamine
Diethyltryptamine
61-51-8
3-(2-Diethylaminoethyl)indole
N,N-Diethyl-2-(1H-indol-3-yl)ethanamine
1H-Indole-3-ethanamine, N,N-diethyl-
INDOLE, 3-(2-(DIETHYLAMINO)ETHYL)-
BRN 0153320
916E8V4S2V
CHEMBL142936
D.E.T.
DTXSID9052763
5-22-10-00050 (Beilstein Handbook Reference)
3-(2-(DIETHYLAMINO)ETHYL)INDOLE
diethyl(2-(1H-indol-3-yl)ethyl)amine
diethyl[2-(1H-indol-3-yl)ethyl]amine
UNII-916E8V4S2V
DEA No. 7434
NN-Diethyltryptamine
Oprea1_105894
SCHEMBL517713
DTXCID7031373
CHEBI:184081
LSSUMOWDTKZHHT-UHFFFAOYSA-N
BDBM50094676
STK368075
AKOS005444987
DB01460
Diethyl-[2-(1H-indol-3-yl)-ethyl]-amine
NS00098694
1H-Indole-3-ethanamine, N,N-diethyl-(9CI)
N,N-Diethyl-2-(1H-indol-3-yl)ethanamine #
C22726
Q2617768
102-975-9
Solubility of N,N-Diethyl-2-(1H-Indol-3-yl)ethanamine
N,N-Diethyl-2-(1H-indol-3-yl)ethanamine, with the chemical formula C14H20N2, exhibits specific solubility characteristics that are noteworthy.
General Solubility Behavior
This compound primarily demonstrates moderate solubility in various organic solvents, often influenced by the presence of the indole structure which contributes to its non-polar character. The following points summarize its solubility:
Factors Affecting Solubility
Several factors can influence the solubility of N,N-diethyl-2-(1H-indol-3-yl)ethanamine, including:
This compound's solubility characteristics can make it a useful candidate in various applications, particularly in **pharmaceutical** formulations where solubility plays a critical role in bioavailability.