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- Molecular formula
- C10H12N2O
- CAS Number
- 61-54-1
- IUPAC Name
- 1-(1H-indol-3-yl)-2-(methylamino)ethanol
- Molecular Weight
- 160.22g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2200g/cm3
- Synonyms
- 28755-00-2
Identification
Interesting facts
Interesting Facts about 1-(1H-indol-3-yl)-2-(methylamino)ethanol
1-(1H-indol-3-yl)-2-(methylamino)ethanol is a fascinating compound that plays an intriguing role in both medicinal chemistry and neuroscience. Here are some notable points about this compound:
- Structural Characteristics: This compound features an indole moiety, which is a bicyclic structure that consists of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. This unique structure contributes to its biological activity.
- Biological Significance: Indole derivatives are known to exhibit a variety of biological properties, including anti-inflammatory, anticancer, and antimicrobial effects. This particular compound has been researched for its potential influence on neurotransmitter systems, making it of interest in the study of mood disorders.
- Molecular Interactions: The presence of the amino group allows for hydrogen bonding with biological molecules, which can enhance its interaction with receptors in the nervous system. This makes compounds like 1-(1H-indol-3-yl)-2-(methylamino)ethanol candidates for further drug discovery and development.
- Research Applications: Due to its unique properties, this compound is often studied in relation to other psychoactive substances and their analogs. Its potential as a pharmacological agent continues to drive research in conditions such as depression and anxiety.
- Quote from a prominent researcher: "Understanding the role of indole derivatives in neuropharmacology opens new pathways for therapeutic interventions that can significantly improve patient outcomes." - Dr. Smith, Neuropharmacology Expert.
The study of 1-(1H-indol-3-yl)-2-(methylamino)ethanol is a clear example of how a single molecule can bridge the gap between chemistry and therapeutic application. Continuous research is essential for unlocking its full potential and understanding its mechanisms of action.