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
Molecular Weight
114.14g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
compared to water.
Synonyms
SCHEMBL3533683
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.

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