Indole-3-acetamide
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- Molecular formula
- C10H10N2O
- CAS Number
- 879-37-8
- IUPAC Name
- 2-(1H-indol-3-yl)acetamide
- Molecular Weight
- 160.20g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1809g/cm3
- Synonyms
- indole-3-acetamide
Identification
Interesting facts
Exploring 2-(1H-indol-3-yl)acetamide: A Unique Compound
2-(1H-indol-3-yl)acetamide is a fascinating compound that belongs to a larger class of molecules known as indole derivatives. As a scientist, you may find this compound intriguing due to its biochemical properties and potential applications. Here are some interesting facts:
- Origin: The indole structure, which is the backbone of this compound, is derived from the fusion of a benzene ring and a pyrrole ring. This unique structure contributes significantly to the biological activity of the compound.
- Biological Significance: Compounds derived from indoles, including 2-(1H-indol-3-yl)acetamide, are known for their role in various biological processes. They have been studied for effects on neurotransmitter activity, showcasing potential in the treatment of mood disorders.
- Potential Therapeutic Uses: Research has indicated that this compound may exhibit anti-inflammatory and analgesic properties. Its structural similarity to neurotransmitters allows it to interact with the brain's receptors, presenting possibilities for neuropharmacology.
- Versatile Synthesis: The synthesis of 2-(1H-indol-3-yl)acetamide can be accomplished through various methods, including the condensation of indole with acetyl chloride. This accessibility makes it an interesting target for organic synthesis and medicinal chemistry.
In summary, 2-(1H-indol-3-yl)acetamide is not just another compound; it embodies a rich tapestry of biochemical potential and synthetic versatility. As you delve into the world of indole derivatives, keep in mind that understanding such compounds can lead to major breakthroughs in medicinal chemistry and therapeutic development.