β-Carboline

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Identification

Molecular formula
C11H8N2O
CAS Number
244-63-3
IUPAC Name
1-vinyl-2H-pyrido[3,4-b]indol-8-ol
Molecular Weight
168.20g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3100g/cm3
Interesting facts

Interesting Facts about 1-vinyl-2H-pyrido[3,4-b]indol-8-ol

1-vinyl-2H-pyrido[3,4-b]indol-8-ol is a fascinating compound that falls within the larger category of indole derivatives. Its unique structure and functional groups lend it several intriguing properties and potential applications:

  • Structural Complexity: The compound features an indole moiety fused with a pyridine ring, making it an interesting subject for organic synthesis and medicinal chemistry.
  • Biological Activity: Compounds like 1-vinyl-2H-pyrido[3,4-b]indol-8-ol have been studied for their biological activities, including potential anti-cancer and anti-inflammatory properties.
  • Research Potential: The vinyl group in its structure makes it a potential candidate for further derivatization, opening avenues for exploring new pharmaceuticals or agrochemicals.
  • Role in Organic Reactions: As a versatile building block, this compound can participate in various organic reactions, such as cycloadditions, cross-couplings, and other reactions that leverage its unsaturated vinyl group.

Furthermore, this compound can potentially serve as a marker in environmental studies, especially in assessing the presence of indole derivatives in natural products. As stated by researchers, "The unique features of indole compounds provide a rich platform for designing novel therapeutics."

As we continue to explore the complexities of compounds like 1-vinyl-2H-pyrido[3,4-b]indol-8-ol, we uncover new insights into their roles within biological systems and their applications in innovative chemical research.

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