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1,1,3-triphenylprop-2-en-1-ol

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Identification
Molecular formula
C21H18O
CAS number
65189-91-1
IUPAC name
1,1,3-triphenylprop-2-en-1-ol
State
State

At room temperature, 1,1,3-triphenylprop-2-en-1-ol is typically a solid, due to its crystalline form.

Melting point (Celsius)
160.00
Melting point (Kelvin)
433.15
Boiling point (Celsius)
420.00
Boiling point (Kelvin)
693.15
General information
Molecular weight
284.37g/mol
Molar mass
284.3680g/mol
Density
0.9978g/cm3
Appearence

1,1,3-Triphenylprop-2-en-1-ol typically appears as a white to off-white crystalline powder. The compound is often used in synthetic chemistry and can be characterized by its distinct crystalline structure.

Comment on solubility

Solubility of 1,1,3-Triphenylprop-2-en-1-ol

1,1,3-Triphenylprop-2-en-1-ol, with its complex structure, exhibits unique solubility characteristics that are influenced by its phenolic structure and hydrophobic side groups. Understanding its solubility is essential for applications in various fields, including organic synthesis and pharmaceuticals.

Key Points on Solubility:

  • Hydrocarbon Nature: The presence of three phenyl rings contributes significantly to its hydrophobic properties, making it less soluble in water.
  • Solvent Compatibility: This compound is more soluble in organic solvents such as ethanol, acetone, or chloroform due to its non-polar characteristics.
  • Temperature Influence: Increased temperature can enhance solubility in organic solvents, allowing for greater dissolution.
  • pH Effect: The hydroxyl group may exhibit varying degrees of solubility depending on the pH of the medium, with potential for increased solubility in alkaline conditions.

In conclusion, while 1,1,3-triphenylprop-2-en-1-ol is generally insoluble in polar solvents like water, it shows favorable solubility in different organic solvents, making it a versatile compound for chemical applications. Understanding these solubility dynamics is crucial for effective utilization in scientific research and industrial processes.

Interesting facts

Exploring 1,1,3-Triphenylprop-2-en-1-ol

1,1,3-Triphenylprop-2-en-1-ol is a fascinating compound that showcases the intricate world of organic chemistry. Often referred to as a stilbene derivative, this compound is notable for several key features:

  • Structure: The compound features a unique structure with three phenyl groups attached to a prop-2-en-1-ol backbone. This arrangement grants it interesting chemical and physical properties.
  • Applications: Derivatives of this compound can be utilized in various applications such as in the development of flavorings, fragrances, and even in the field of pharmaceuticals.
  • Reactivity: The presence of the olefinic bond (the double bond in the prop-2-en) makes it reactive and allows it to participate in various chemical reactions, including addition reactions which are significant in synthetic organic chemistry.

Biological Aspects

Research has indicated that polyphenolic compounds, similar to 1,1,3-triphenylprop-2-en-1-ol, may exhibit antioxidant properties. These compounds are believed to contribute to the health benefits of certain plants and could play a role in:

  • Reducing oxidative stress
  • Potential anti-inflammatory effects
  • Exhibiting antimicrobial activity

“Chemistry is the science of matter, but I prefer to see it as the science of change.” This quote by Wilhelmina Geddes aptly reflects the characteristics of 1,1,3-triphenylprop-2-en-1-ol, which changes its behavior and interacts with various substances. Scientists continue to study this compound, recognizing the potential it holds in both industrial and research settings.

Synonyms
Diphenylstyrylcarbinol
NCIOpen2_004453
Oprea1_155302
DTXSID401262366
1,1,3-Triphenyl-prop-2-en-1-ol
I+/--Phenyl-I+/--(2-phenylethenyl)benzenemethanol