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3-Phenyl-1-butene

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Identification
Molecular formula
C10H12
CAS number
768-65-8
IUPAC name
but-3-enylbenzene
State
State

3-Phenyl-1-butene is a liquid at room temperature.

Melting point (Celsius)
-75.00
Melting point (Kelvin)
198.15
Boiling point (Celsius)
185.00
Boiling point (Kelvin)
458.15
General information
Molecular weight
130.19g/mol
Molar mass
130.1870g/mol
Density
0.8645g/cm3
Appearence

3-Phenyl-1-butene is a colorless liquid. It has a characteristic aromatic odor typical of simple hydrocarbons.

Comment on solubility

Solubility of But-3-enylbenzene

But-3-enylbenzene, known for its unique structure, displays several intriguing characteristics regarding its solubility. This compound, which contains both a but-3-enyl group and a benzene ring, is primarily characterized by its hydrophobic nature.

Key Solubility Points:

  • Nonpolar Nature: The presence of the large benzene ring contributes to the nonpolar characteristics of but-3-enylbenzene, making it less soluble in polar solvents like water.
  • Solubility in Organic Solvents: This compound shows good solubility in various organic solvents such as alcohols, ethers, and hydrocarbons. Some typical examples include:
    • Ether
    • Benzene
    • Acetone
  • Influence of Temperature: Like many organic compounds, the solubility of but-3-enylbenzene tends to increase with temperature, indicating a thermodynamic dependency on solvation processes.

In summary, while but-3-enylbenzene is insoluble in water due to its nonpolar nature, it readily dissolves in a range of organic solvents, making it versatile for various chemical applications and reactions.

Interesting facts

Interesting Facts about But-3-enylbenzene

But-3-enylbenzene, also known as 3-butenylbenzene, is a fascinating compound that belongs to the family of aromatic hydrocarbons. This compound is notable for its unique structure and potential applications in various fields.

Key Features

  • Subclass of Aromatic Compounds: It combines the properties of both alkenes and aromatic compounds, offering a rich area of study for chemists interested in reaction mechanisms.
  • Reactivity: The presence of the vinyl group (but-3-enyl) allows for interesting reactivity, particularly in polymer chemistry and as a precursor in synthesizing other complex molecules.
  • Applications: But-3-enylbenzene is being explored in the development of advanced materials, including specialty polymers and as an additive in pharmaceuticals.

Practical Implications

Its unique structure leads to intriguing properties; for example, the allylic position adjacent to the double bond can be engaged in various reactions, making it a valuable building block in organic synthesis.

Research and Development

Current studies are focusing on the compound's behavior in different catalytic processes, as well as its potential uses in creating new materials with enhanced properties. The field of green chemistry also shows promise, with interest in sustainable pathways for its synthesis.

In conclusion, but-3-enylbenzene extends beyond just being an organic compound; it presents a multitude of opportunities for research and application, inviting chemists to explore its potential in innovative ways.

Synonyms
4-PHENYL-1-BUTENE
768-56-9
3-Butenylbenzene
3-buten-1-ylbenzene
Benzene, 3-buten-1-yl-
NSC 65603
UNII-58584HOZ1Z
58584HOZ1Z
NSC-65603
DTXSID80227612
EC 405-980-7
DTXCID30150103
pbgvmidtggtbfs-uhfffaoysa-n
but-3-enylbenzene
Benzene, 3-butenyl-
1-Phenyl-3-butene
1-Butene, 4-phenyl-
4-Phenylbutene-1
4-Phenylbut-1-ene
(but-3-en-1-yl)benzene
but-3-enyl-benzene
but-3-en-1-ylbenzene
MFCD00026111
4-phenyl butene
NCIOpen2_000307
4-Phenyl-1-butene, 99%
WLN: 1U3R
AAA76856
NSC65603
AKOS009156430
AC-16193
LS-13774
DB-056146
NS00005147
P0161
D91916
EN300-134660
Q27261558
YGM