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2-Fluoro-1-(2,2-diphenylvinyl)benzene

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Identification
Molecular formula
C20H15F
CAS number
167306-28-1
IUPAC name
1-(2,2-diphenylvinyl)-2-fluoro-benzene
State
State

At room temperature, 2-Fluoro-1-(2,2-diphenylvinyl)benzene is typically found in a solid state.

Melting point (Celsius)
123.00
Melting point (Kelvin)
396.15
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
272.32g/mol
Molar mass
272.3190g/mol
Density
1.0880g/cm3
Appearence

2-Fluoro-1-(2,2-diphenylvinyl)benzene typically appears as a solid compound. Its color can range from white to off-white depending on its purity.

Comment on solubility

Solubility of 1-(2,2-diphenylvinyl)-2-fluoro-benzene

1-(2,2-diphenylvinyl)-2-fluoro-benzene exhibits an interesting profile when it comes to its solubility properties. Here are some key points to consider:

  • Polarity: The compound features a combination of aromatic rings and a fluorine atom, which can impact its solubility in different solvents.
  • Solvent Compatibility: Typically, compounds with significant aromatic content tend to be insoluble in polar solvents like water but may dissolve well in organic solvents, such as:
    • Hexane
    • Toluene
    • Chloroform
  • Hydrophobic Interactions: The substantial hydrophobic character of the diphenyl groups suggests that it prefers to interact with non-polar environments, reinforcing its low solubility in polar mediums.

In conclusion, while 1-(2,2-diphenylvinyl)-2-fluoro-benzene is likely to exhibit limited solubility in water, it shows a preference for dissolution in organic solvents, highlighting the importance of understanding a compound’s structure to predict its solubility behavior.

Interesting facts

Interesting Facts about 1-(2,2-Diphenylvinyl)-2-fluoro-benzene

1-(2,2-diphenylvinyl)-2-fluoro-benzene, an intriguing organic compound, is known for its unique structure and versatile applications. Here are some fascinating aspects of this compound:

  • Structural Complexity: The compound features a sophisticated arrangement characterized by a vinyl group bonded to a fluoro-substituted phenyl ring. This complexity opens doors to various chemical reactions and modifications.
  • Fluorine's Influence: The presence of the fluorine atom significantly affects the compound's reactivity and stability. Fluorine, being highly electronegative, can enhance certain chemical properties, making this compound interesting for synthetic applications.
  • Photophysical Properties: Compounds like 1-(2,2-diphenylvinyl)-2-fluoro-benzene often exhibit exceptional photophysical behaviors. They can show interesting photoluminescence characteristics, making them suitable candidates for optical devices and imaging technologies.
  • Potential Applications: This compound can serve as a building block for more complex structures in materials science and organic electronics, such as in light-emitting diodes (LEDs) and solar cells.
  • Research and Development: Ongoing research into compounds of this nature contributes to advancements in photonic materials and organic synthesis methodologies. Scientists continue to explore their properties to unlock new functionalities.

As a fascinating intersection of chemistry and technology, 1-(2,2-diphenylvinyl)-2-fluoro-benzene exemplifies the innovative spirit of materials science, encouraging further investigation into its potential applications and underlying mechanisms of behavior.

Synonyms
ETHYLENE, 1,1-DIPHENYL-2-(o-FLUOROPHENYL)-
1229-68-1
BRN 2530092
1,1-Diphenyl-2-(o-fluorophenyl)ethylene
DTXSID80153780