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Allyl ethylene glycol formal

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Identification
Molecular formula
C6H10O2
CAS number
4887-44-9
IUPAC name
2-prop-1-enyl-1,3-dioxolane
State
State

At room temperature, 2-prop-1-enyl-1,3-dioxolane is in a liquid state. This clear, colorless liquid is typically very fluid and can be poured easily due to its low viscosity and density compared to water.

Melting point (Celsius)
-75.00
Melting point (Kelvin)
198.15
Boiling point (Celsius)
108.50
Boiling point (Kelvin)
381.65
General information
Molecular weight
114.14g/mol
Molar mass
114.1440g/mol
Density
0.9518g/cm3
Appearence

2-Prop-1-enyl-1,3-dioxolane appears as a clear, colorless liquid. Its distinct characteristic is its clear transparency, making it easily distinguishable by its lack of color and typical liquid appearance.

Comment on solubility

Solubility of 2-prop-1-enyl-1,3-dioxolane

2-prop-1-enyl-1,3-dioxolane, a cyclic ether derivative, has a solubility profile that is influenced by its unique molecular structure. Here are some key points regarding its solubility:

  • Polarity: The presence of the dioxolane ring contributes to the compound's moderate polarity. This may enhance its solubility in polar solvents.
  • Solvent Compatibility: 2-prop-1-enyl-1,3-dioxolane is likely soluble in:
    • Water (to a limited extent)
    • Alcohols (e.g., ethanol, methanol)
    • Other polar organic solvents (e.g., acetone)
  • Hydrophobic Interactions: The aliphatic propene substituent may reduce solubility in highly polar solvents but can improve solubility in less polar organic compounds.

In conclusion, while the solubility of 2-prop-1-enyl-1,3-dioxolane can vary depending on environmental conditions such as temperature and pressure, understanding its polarity and functional groups can provide insight into its behavior in different solvents. As solubility is a critical aspect in many chemical processes, the application of this compound may rely heavily on its solubility characteristics.

Interesting facts

Interesting Facts about 2-prop-1-enyl-1,3-dioxolane

2-prop-1-enyl-1,3-dioxolane is an intriguing compound that belongs to the family of dioxolanes, which are cyclic compounds characterized by a five-membered ring featuring two oxygen atoms. Here are some fascinating aspects of this chemical:

  • Structural Versatility: The structure of 2-prop-1-enyl-1,3-dioxolane includes a vinyl group, which significantly enhances its reactivity. This feature makes it exceptionally useful in organic synthesis.
  • Applications in Synthesis: It serves as an important intermediate in the synthesis of various complex organic compounds. Its ability to participate in reactions such as ring-opening polymerization highlights its utility in creating polymers and related materials.
  • Reactivity: The presence of the dioxolane ring contributes to its reactivity, allowing it to stabilize carbocations and facilitating transformations that are crucial in synthetic chemistry.
  • Research Potential: Studies on dioxolane derivatives like 2-prop-1-enyl-1,3-dioxolane continue to reveal novel chemical properties and reactions, making it a subject of ongoing research in the field of organic chemistry.
  • Environmental Implications: Dioxolanes degrade more readily than other cyclic ethers, which is a relevant factor to consider in terms of environmental impact and sustainability in chemical applications.

In summary, 2-prop-1-enyl-1,3-dioxolane is not just another chemical compound; it's a gateway to understanding more complex organic transformations, with applications that can potentially shape innovate practices in materials science and environmental chemistry.

Synonyms
SCHEMBL3533683