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3-Acetylstilbene

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Identification
Molecular formula
C16H14O
CAS number
645-49-8
IUPAC name
1-(3-styrylphenyl)ethanone
State
State

At room temperature, 3-acetylstilbene is generally found in a solid state, appearing as white to light yellow crystals.

Melting point (Celsius)
89.00
Melting point (Kelvin)
362.15
Boiling point (Celsius)
387.00
Boiling point (Kelvin)
660.15
General information
Molecular weight
208.27g/mol
Molar mass
208.2650g/mol
Density
1.1124g/cm3
Appearence

3-Acetylstilbene is a solid compound that typically appears as white to light yellow crystals. The solid form is crystalline and may also sometimes be described as a powder.

Comment on solubility

Solubility of 1-(3-styrylphenyl)ethanone

1-(3-styrylphenyl)ethanone, a compound with intriguing structural characteristics, displays unique solubility properties. Understanding its solubility behavior is crucial for various applications in chemical processes and formulations.

In general, the solubility of this compound can be influenced by several factors:

  • Polarity: Due to the presence of both aromatic and carbonyl groups, 1-(3-styrylphenyl)ethanone is expected to exhibit moderate polarity, which can enhance its solubility in polar organic solvents.
  • Solvent Compatibility: It tends to be soluble in solvents like ethanol, acetone, and other similar polar organic solvents, while its solubility in water is likely to be limited.
  • Temperature Effects: As with many organic compounds, the solubility of 1-(3-styrylphenyl)ethanone can increase with temperature, making it easier to dissolve at elevated temperatures.

As a general rule, “like dissolves like,” so the choice of solvent is crucial when working with 1-(3-styrylphenyl)ethanone. If you want to explore potential reactions or formulations involving this compound, consider the solvent's polarity and temperature conditions to optimize solubility.

Interesting facts

Interesting Facts about 1-(3-Styrylphenyl)ethanone

1-(3-Styrylphenyl)ethanone, commonly known in chemical circles as a derivative of acetophenone, is a fascinating compound that captures the attention of many chemists due to its unique structure and potential applications. Here are some intriguing insights:

  • Structural Characteristics: This compound features an ethanone core with a styryl group substituted at the 3-position of the phenyl ring. Its geometric configuration allows for interesting reactivity and potential interactions with other molecules.
  • Applications in Organic Synthesis: The compound serves as a useful intermediate in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals. Its reactivity can lead to significant transformations that are valuable in chemical research.
  • Photophysical Properties: Due to its conjugated system, 1-(3-styrylphenyl)ethanone exhibits interesting photophysical properties, making it a candidate for applications in materials science, such as organic light-emitting diodes (OLEDs).
  • Biological Activities: Studies suggest that derivatives of this compound may exhibit biological activities, such as anti-inflammatory and anti-cancer properties, which make it a potential target in medicinal chemistry.

As chemists explore the flexibility and reactivity of 1-(3-styrylphenyl)ethanone, they continue to uncover new possibilities that may lead to innovative applications across various fields, including materials science and pharmaceuticals. This compound illustrates how small changes in molecular structure can have far-reaching effects in chemical properties and potential uses.

"The beauty of chemistry lies in its ability to turn complex substances into tools for innovation."

Synonyms
59089-10-0
1-[3-(2-PHENYLETHENYL)PHENYL]ETHANONE
Ethanone, 1-[3-(2-phenylethenyl)phenyl]-
DTXSID80274545