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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
State
State
This compound is a solid at room temperature.
Melting point (Celsius)
144.00
Melting point (Kelvin)
417.15
Boiling point (Celsius)
258.00
Boiling point (Kelvin)
531.15
General information
Molecular weight
168.20g/mol
Molar mass
168.1960g/mol
Density
1.3100g/cm3
Appearence

β-Carboline is typically a crystalline solid that may appear as colorless or slightly yellow crystals. These crystals can have a sheen and may form needle or plate-like structures depending on the specific form or salt of the compound.

Comment on solubility

Solubility of 1-vinyl-2H-pyrido[3,4-b]indol-8-ol

The solubility of 1-vinyl-2H-pyrido[3,4-b]indol-8-ol (C11H8N2O) can be intriguing due to its unique structural features. Understanding its solubility is key for applications in chemical synthesis and pharmaceuticals.

Key Factors Influencing Solubility

  • Polarity: As a nitrogen-containing heterocycle, its solubility may vary in polar and nonpolar solvents.
  • Hydroxyl Group: The presence of the hydroxyl (–OH) group typically enhances solubility in polar solvents like water.
  • Molecular Structure: The complex structure may affect how it interacts with various solvents, potentially leading to variable solubility behaviors.

Solvent Interaction

  • It may dissolve well in organic solvents such as ethanol and dimethyl sulfoxide (DMSO).
  • Contrarily, its solubility in water may be limited but could improve with temperature and pH adjustments.

In summary, the solubility of 1-vinyl-2H-pyrido[3,4-b]indol-8-ol is dictated by multiple factors, and understanding them allows for better utilization in various chemical processes. Further research may provide insights into optimizing its solubility for practical applications.

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.