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1,2-Divinylcyclobutane

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Identification
Molecular formula
C8H12
CAS number
1551-01-3
IUPAC name
1,2-divinylcyclobutane
State
State

At room temperature, 1,2-Divinylcyclobutane is a liquid due to its low melting point.

Melting point (Celsius)
-85.00
Melting point (Kelvin)
188.15
Boiling point (Celsius)
97.00
Boiling point (Kelvin)
370.15
General information
Molecular weight
108.18g/mol
Molar mass
108.1810g/mol
Density
0.7663g/cm3
Appearence

1,2-Divinylcyclobutane is a clear, colorless liquid. It has a sharp, flammable odor characteristic of many hydrocarbons.

Comment on solubility

Solubility of 1,2-Divinylcyclobutane

1,2-Divinylcyclobutane is a unique compound with intriguing solubility characteristics. Its solubility can be influenced by several factors, primarily due to its molecular structure and the presence of multiple vinyl groups. Here’s a closer look at its solubility:

  • Polar vs. Non-Polar: 1,2-Divinylcyclobutane is generally considered non-polar due to its hydrocarbon structure. As a result, it tends to dissolve better in organic solvents rather than in polar solvents like water.
  • Solvent Compatibility: It is typically soluble in:
    • Hydrocarbons (e.g., hexane, octane)
    • Aromatic solvents (e.g., benzene, toluene)
  • Temperature Effects: The solubility may also increase with temperature, a common phenomenon in organic compounds.
  • Chemical Stability: When dissolved, it can still maintain its integrity, making it useful in various applications where a stable solution is required.

In summary, the solubility of 1,2-divinylcyclobutane is largely dictated by its non-polar nature, which favors dissolution in non-polar solvents. This compound exemplifies the principle of “like dissolves like,” reinforcing the importance of considering solvent properties in solubility assessments.

Interesting facts

Interesting Facts About 1,2-Divinylcyclobutane

1,2-Divinylcyclobutane is an intriguing compound that has captured the attention of chemists due to its unique structure and properties. Here are some fascinating insights:

  • Structural Features: This compound features a cyclobutane ring with two vinyl groups attached at the 1 and 2 positions. This configuration leads to interesting reactivity and stability patterns.
  • Polymerization Potential: 1,2-Divinylcyclobutane can undergo polymerization, making it a valuable monomer in the production of various polymers. Its ability to form cross-links contributes to the creation of strong, resilient materials.
  • Synthesis: The synthesis of this compound can include methods such as cycloaddition reactions or vinylation processes, showcasing the versatility of synthetic organic chemistry.
  • Applications in Research: The compound is not just a subject of academic curiosity; it has potential applications in fields such as materials science and organic electronics.
  • Reactivity: Due to the strained nature of the cyclobutane ring and the presence of the double bonds, 1,2-divinylcyclobutane exhibits a range of unique chemical properties, including susceptibility to undergo further reactions under certain conditions.
  • Future Directions: Ongoing research seeks to explore its potential in new applications, underlining the importance of compounds like this in advancing chemical science.

As chemists continue to investigate and understand such unique compounds, we unlock the door to innovations in various industrial applications, opening new avenues for exploration and discovery.

Synonyms
1,2-DIVINYLCYCLOBUTANE
2422-85-7
1,2-DIETHENYLCYCLOBUTANE
cis-1,2-Divinylcyclobutane
Cyclobutane, 1,2-divinyl-, trans-
trans-1,2-Divinylcyclobutane
cis-1,2-Diethenyl-cyclobutane
Cyclobutane, 1,2-divinyl-
Cyclobutane, 1,2-diethenyl-
Cyclobutane, 1,2-diethenyl-, trans-
DTXSID30871164
16177-46-1