3-Methyl-1H-indole-1-ethanone

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Identification

Molecular formula
C11H11NO
CAS Number
38097-16-0
IUPAC Name
1-(3-methylindol-1-yl)ethanone
Molecular Weight
173.22g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1458g/cm3
Synonyms
N-Acetyl-3-methylindole
Interesting facts

Interesting Facts About 1-(3-methylindol-1-yl)ethanone

1-(3-methylindol-1-yl)ethanone, also known as a derivative of indole, holds significant importance in various fields of chemistry and biochemistry. Here are some intriguing insights about this compound:

  • Structural Significance: The presence of the indole ring—a bicyclic structure consisting of a benzene fused to a pyrrole—enriches its chemical properties. This unique structure allows for diverse interactions with biological systems.
  • Biological Relevance: Compounds derived from indole are well-known for their various biological activities. They can exhibit anti-cancer, anti-inflammatory, and anti-microbial properties, marking them as valuable targets in the development of pharmaceuticals.
  • Synthesis Enthusiasm: The synthesis of 1-(3-methylindol-1-yl)ethanone can be an exciting challenge for chemists. In particular, it typically involves approaches like the Friedel-Crafts acylation, which is a fundamental reaction in organic synthesis.
  • Flavor and Aroma: Some indole derivatives, including those related to 1-(3-methylindol-1-yl)ethanone, are known for their distinct scents. Indole itself can impart a floral or fecal aroma depending on concentration, showcasing its versatility in flavor chemistry.
  • Research Applications: The study of indole derivatives is a hot topic in medicinal chemistry. Their role in neurotransmission and modulation of certain dopamine receptors has sparked interest among researchers studying neurochemistry and psychology.

As the vast array of applications and properties associated with this compound continues to unfold, 1-(3-methylindol-1-yl)ethanone stands as a testament to the richness of organic chemistry and its pivotal role in drug discovery and development.


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