Tryptamine
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- Molecular formula
- C10H12N2
- CAS Number
- 61-54-1
- IUPAC Name
- 4-(1H-indol-3-yl)butan-2-amine
- Molecular Weight
- 160.22g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1690g/cm3
- Synonyms
- 4-(1H-indol-3-yl)butan-2-amine
Identification
Interesting facts
Interesting Facts about 4-(1H-indol-3-yl)butan-2-amine
4-(1H-indol-3-yl)butan-2-amine, also known as 4-(Indol-3-yl)butan-2-amine, is a fascinating compound that falls within the category of indole derivatives. These types of compounds exhibit a wide range of biological activities and have made a significant impact in medicinal chemistry. Here are some intriguing aspects of this compound:
- Biological Relevance: Compounds that feature an indole moiety are often found in various natural products, particularly those that exhibit important pharmacological effects. Indoles are known for their roles in neurotransmission, inflammation, and as potential antidepressants.
- Potential Therapeutic Uses: 4-(1H-indol-3-yl)butan-2-amine has garnered attention for its possible application in treating neurological disorders, with studies suggesting it may have neuroprotective properties.
- Research Highlights: A multitude of studies are dedicated to understanding the mechanisms of indole derivatives. Specific investigations explore their interactions with serotonin receptors, which are critical for mood regulation.
- Structural Significance: The unique structure of 4-(1H-indol-3-yl)butan-2-amine, characterized by the combination of the indole ring and the aliphatic amine group, contributes to its chemical reactivity and biological interactions, making it an interesting target for synthetic chemists.
- Synthetic Pathways: Chemists have devised several synthetic methods to produce this compound, many of which emphasize the importance of protecting functional groups during reactions to achieve high yields and purity.
As a compound with connections to both natural and synthetic chemistry, 4-(1H-indol-3-yl)butan-2-amine continues to be a rich subject for research. Its exploration not only helps us better understand complex biochemical pathways but also opens up avenues for the development of novel therapeutic agents.