5-Methoxy-N,N-dimethyltryptamine

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Identification

Molecular formula
C13H18N2S
CAS Number
1019-45-0
IUPAC Name
N-methyl-2-(5-methylsulfanyl-1H-indol-3-yl)ethanamine
Molecular Weight
218.36g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2400g/cm3
Synonyms
BRN 0394069
Interesting facts

Interesting Facts About N-methyl-2-(5-methylsulfanyl-1H-indol-3-yl)ethanamine

N-methyl-2-(5-methylsulfanyl-1H-indol-3-yl)ethanamine is a fascinating compound that belongs to the class of indole derivatives, which are notable for their extensive presence in natural products and biological systems. Here are some captivating insights about this compound:

  • Structural Significance: The indole ring structure plays a vital role in medicinal chemistry, often serving as a scaffold for various pharmacologically active compounds.
  • Biological Activity: Compounds containing indole moieties have been found to exhibit a wide range of biological activities, including anti-inflammatory, anti-cancer, and anti-viral properties.
  • Methylsulfanyl Group: The presence of the methylsulfanyl substituent adds unique properties to this compound, potentially affecting its reactivity and interaction with biological targets.
  • Research Applications: This compound is of significant interest in the pharmaceutical industry, where it might be explored for drug development due to its structural analogies with known therapeutic agents.
  • Challenges and Opportunities: While N-methyl-2-(5-methylsulfanyl-1H-indol-3-yl)ethanamine shows promise, challenges in synthesis and understanding its mechanism of action invite ongoing research in the field of organic and medicinal chemistry.

In summary, N-methyl-2-(5-methylsulfanyl-1H-indol-3-yl)ethanamine is not just a simple compound; it encapsulates a world of possibilities in the intersection of organic synthesis and drug discovery. As researchers delve deeper into its properties, we may uncover even more intriguing applications that could benefit science and medicine alike.

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