1-(benzothiophen-3-yl)-2-(1-piperidyl)ethanone

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Identification

Molecular formula
C15H17NOS
CAS Number
171068-86-9
IUPAC Name
1-(benzothiophen-3-yl)-2-(1-piperidyl)ethanone
Molecular Weight
245.37g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1563g/cm3
Interesting facts

Exploring 1-(Benzothiophen-3-yl)-2-(1-piperidyl)ethanone

1-(Benzothiophen-3-yl)-2-(1-piperidyl)ethanone is a fascinating compound with several intriguing characteristics and potential applications. As a derivative of benzothiophene, it incorporates a benzothiophene moiety, which is well-known for its diverse biological activities. Here are some interesting facts about this compound:

  • Biological Significance: Compounds containing benzothiophene structures have been reported to exhibit a variety of pharmacological effects, including anti-inflammatory, antioxidant, and anticancer properties.
  • Neurochemical Potential: The presence of the piperidine ring opens avenues for research into neurochemical interactions, suggesting possible benefits in the field of neuropharmacology.
  • Synthetic Versatility: The synthesis of such aromatic compounds can often be approached with various synthetic methodologies, showcasing the flexibility in organic chemistry.
  • Research Interest: Given the compound's structural features, it's a subject of interest in drug development, particularly for targeting specific enzymes or receptors in biological systems.

In conclusion, 1-(benzothiophen-3-yl)-2-(1-piperidyl)ethanone stands at the crossroads of organic chemistry and pharmacological research. As scholars delve into its properties and potential applications, the compound serves as a reminder of the complex relationships between chemical structure and biological activity, inviting further exploration and discovery.

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