N/A

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Identification

Molecular formula
C16H17NO3
CAS Number
459868-92-9
IUPAC Name
2-(1,8-diethyl-4,9-dihydro-3H-pyrano[3,4-b]indol-1-yl)acetic acid
Molecular Weight
271.32g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2700g/cm3
Appearance
could vary slightly depending on the form used, but it generally retains a fine crystalline or powder-like appearance.
Synonyms
etodolac
Interesting facts

Interesting Facts about 2-(1,8-diethyl-4,9-dihydro-3H-pyrano[3,4-b]indol-1-yl)acetic Acid

This intriguing compound, known scientifically as 2-(1,8-diethyl-4,9-dihydro-3H-pyrano[3,4-b]indol-1-yl)acetic acid, is notable for its unique structure and potential applications in various fields. Here are some fascinating insights:

  • Complex Structure: The compound features a multi-ring structure that provides stability and may influence its reactivity. The pyranoindole framework is particularly significant due to its incorporation of nitrogen in a heterocyclic system.
  • Potential Therapeutic Applications: Compounds like this one may have implications in medicinal chemistry, particularly in developing drugs targeting neurological or psychological disorders, owing to their indole-like structure, which is often found in many biologically active substances.
  • Synthetic Interest: The synthesis of this compound could represent challenges and opportunities for chemists. Researchers may explore innovative synthetic routes that could lead to the discovery of new analogs with enhanced activity.
  • Natural Product Inspiration: The design of this compound may draw inspiration from natural products known for their psychoactive properties. Understanding its mechanism of action could unveil new pathways for drug development.

As you explore this compound further, consider the broader implications of its structure and potential applications in both pharmaceutical sciences and organic chemistry. The intersection of synthetic methods and biological activity remains a thrilling area of study for advancing scientific knowledge.

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