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1-Phenylpyridinium-3-ol

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Identification
Molecular formula
C11H9NO
CAS number
60343-72-4
IUPAC name
1-phenylpyridin-1-ium-3-ol
State
State

This compound is typically a solid at room temperature.

Melting point (Celsius)
180.00
Melting point (Kelvin)
453.15
Boiling point (Celsius)
295.00
Boiling point (Kelvin)
568.15
General information
Molecular weight
185.21g/mol
Molar mass
185.2110g/mol
Density
1.2100g/cm3
Appearence

1-Phenylpyridinium-3-ol typically appears as a crystalline solid. The appearance of the compound can vary in color, but it often presents as a white or off-white powder.

Comment on solubility

Solubility of 1-phenylpyridin-1-ium-3-ol

1-phenylpyridin-1-ium-3-ol, characterized by its unique structure, exhibits intriguing solubility properties that can greatly affect its applications. Solubility is often influenced by various factors such as polarity, the presence of functional groups, and intermolecular interactions. Here are some key points regarding the solubility of this compound:

  • Polarity: The presence of the hydroxyl group (-OH) in 1-phenylpyridin-1-ium-3-ol enhances its polar character, suggesting that it may be soluble in polar solvents such as water.
  • Hydrogen Bonding: The -OH group can engage in hydrogen bonding, which typically increases solubility in polar environments while reducing solubility in nonpolar solvents.
  • Aromatic Stacking: Its phenyl group can engage in π-π stacking interactions, which may affect solubility in organic solvents.
  • pH Dependence: The solubility of ionic compounds such as 1-phenylpyridin-1-ium-3-ol can also be influenced by the pH of the solution, potentially leading to better solubility in acidic conditions.

In summary, while 1-phenylpyridin-1-ium-3-ol showcases a propensity towards solubility in polar solvents, it's essential to consider all influencing factors for a comprehensive understanding. As the famous saying goes, "The solution often lies within the structure itself."

Interesting facts

Interesting Facts about 1-Phenylpyridin-1-ium-3-ol

1-Phenylpyridin-1-ium-3-ol, a fascinating compound, belongs to the family of pyridinium derivatives. This compound features a pyridine ring, which is a six-membered aromatic ring with one nitrogen atom. The unique structure of this compound contributes to several intriguing properties and applications in various fields:

  • Biological significance: Studies have shown that pyridine derivatives can exhibit various biological activities, including antimicrobial, antifungal, and anti-inflammatory effects. This makes compounds like 1-phenylpyridin-1-ium-3-ol of great interest in medicinal chemistry.
  • Protonated form: The presence of the pyridin-1-ium moiety indicates that this compound can exist in a protonated form, making it a strong candidate for studies in proton transfer reactions and its behavior in different pH environments.
  • Synthetic versatility: This compound can serve as a versatile building block in organic synthesis, offering potential routes to more complex organic molecules. Its structure can be tailored for various applications in pharmaceuticals and agrochemicals.
  • Potential in materials science: Research is exploring the use of pyridinium derivatives in the development of ionic liquids and as functional materials for electronic devices due to their charge properties and thermal stability.
  • Fluorescent properties: Some pyridine derivatives display interesting fluorescence properties, which opens up new avenues in fields such as sensing and imaging technologies.

In summary, 1-phenylpyridin-1-ium-3-ol is more than just a chemical compound; it represents a versatile platform for further research and application across a spectrum of scientific disciplines. As researchers and practitioners in the field of chemistry continue to uncover its potential, the compound stands as a testament to the richness of organic chemistry and its impact on innovation.

Synonyms
3-hydroxy-1-phenylpyridinium
SCHEMBL17265782
AG-777/25006423