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4-Vinylphenol

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Identification
Molecular formula
C8H8O
CAS number
2628-17-3
IUPAC name
4-but-2-enylphenol
State
State

At room temperature, 4-vinylphenol exists as a liquid. Although it may partially crystallize near or below its melting point, slight variations in temperature around room temperature can influence its physical state.

Melting point (Celsius)
10.00
Melting point (Kelvin)
283.15
Boiling point (Celsius)
225.00
Boiling point (Kelvin)
498.15
General information
Molecular weight
120.15g/mol
Molar mass
120.1510g/mol
Density
1.0440g/cm3
Appearence

4-Vinylphenol is typically characterized as a colorless to pale yellow liquid. Due to its phenolic structure, it can also exhibit mild to moderate aromatic odors reminiscent of natural phenols.

Comment on solubility

Solubility of 4-but-2-enylphenol (C8H8O)

4-but-2-enylphenol, with the chemical formula C8H8O, exhibits interesting solubility characteristics that are influenced by its molecular structure. Here are some key points regarding its solubility:

  • Polarity: Due to the presence of the hydroxyl (-OH) group in its structure, 4-but-2-enylphenol demonstrates moderate polarity. This makes it somewhat soluble in polar solvents.
  • Solvent Compatibility: It is more soluble in organic solvents, such as ethanol and acetone, compared to water. This is indicative of its compatibility with non-polar solvents.
  • Temperature Dependency: The solubility can vary with temperature; as the temperature increases, solubility in organic solvents may also increase, facilitating better dissolution.
  • Hydroxyl Effects: The hydroxyl group can engage in hydrogen bonding, further enhancing interactions with other molecules which may aid solubility in specific conditions.

In summary, while 4-but-2-enylphenol shows moderate solubility in polar solvents, its best solubility is achieved in organic solvents, making it versatile for various applications in chemical processes. This compound's solubility behavior exemplifies the crucial role of functional groups in determining interactions in different solvent environments.

Interesting facts

Interesting Facts about 4-But-2-enylphenol

4-But-2-enylphenol is a fascinating compound that belongs to the family of phenolic compounds, which are crucial in various biological and chemical processes. Here are some intriguing insights about this compound:

  • Versatile Applications: 4-But-2-enylphenol plays a significant role in the synthesis of various chemicals and pharmaceuticals, often being used as an intermediate in organic reactions.
  • Natural Sources: This compound can be found in certain plants where it may contribute to their unique properties, including flavors and fragrances.
  • Functional Groups: The presence of the vinyl group (double bond) makes 4-but-2-enylphenol quite reactive, allowing it to participate in a range of organic reactions such as polymerization and cross-coupling.
  • Biological Relevance: The phenolic structure is essential in medicinal chemistry, with related compounds having antioxidant and antimicrobial properties. While specific studies on 4-but-2-enylphenol are limited, its structural analogs are indeed known for these beneficial effects.
  • Research Potential: There is ongoing research into the applications of this compound in materials science and nanotechnology, exploring its potential in creating new and innovative materials.

In summary, 4-but-2-enylphenol not only demonstrates the diverse chemistry of phenolic compounds but also highlights the continuous pursuit of scientists to unlock their potential in various fields. Research into this compound opens avenues for discovering new applications that could benefit multiple sectors.

Synonyms
p-2-Butenylphenol
SCHEMBL111720
SCHEMBL11829476