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2-Styryl-1,3-dioxolane

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Identification
Molecular formula
C11H12O2
CAS number
51518-54-6
IUPAC name
2-styryl-1,3-dioxolane
State
State

At room temperature, 2-styryl-1,3-dioxolane is a liquid.

Melting point (Celsius)
-10.00
Melting point (Kelvin)
263.15
Boiling point (Celsius)
268.00
Boiling point (Kelvin)
541.15
General information
Molecular weight
176.22g/mol
Molar mass
176.2150g/mol
Density
1.0612g/cm3
Appearence

2-Styryl-1,3-dioxolane typically appears as a colorless to pale yellow liquid. It is characterized by its clear and translucent nature.

Comment on solubility

Solubility of 2-styryl-1,3-dioxolane

2-styryl-1,3-dioxolane, a compound characterized by its unique structure, exhibits interesting solubility properties. Being a dioxolane derivative, it tends to dissolve in certain organic solvents while having limited solubility in polar solvents.

Key Points on Solubility:

  • Solvent Compatibility: 2-styryl-1,3-dioxolane is generally soluble in nonpolar organic solvents, such as hexane, benzene, and chloroform.
  • Poor Solubility in Water: This compound exhibits very low solubility in water due to its hydrophobic nature, making it less effective in aqueous solutions.
  • Temperature Effects: It is important to note that solubility can be affected by temperature; increased temperatures often lead to enhanced solubility in organic solvents.
  • Structural Influence: The presence of the styryl group contributes to its solubility pattern, as it introduces aromatic characteristics that interact favorably with nonpolar solvents.

Understanding the solubility of 2-styryl-1,3-dioxolane is crucial for applications in chemical synthesis and formulation, especially when considering its behavior in various solvent systems.

Interesting facts

Interesting Facts about 2-Styryl-1,3-Dioxolane

2-Styryl-1,3-dioxolane is a fascinating compound within the realm of organic chemistry, known for its unique structural features and potential applications. Here are some intriguing points about this compound:

  • Structural Significance: The presence of a dioxolane ring within the structure provides properties that can be manipulated for various chemical reactions. This makes it a versatile building block in synthetic organic chemistry.
  • Applications in Medicine: Dioxolane derivatives have shown promise in medicinal chemistry. The incorporation of aromatic styryl groups can enhance biological activity, making compounds like 2-styryl-1,3-dioxolane relevant in drug design.
  • Polymer Chemistry: 2-Styryl-1,3-dioxolane can be used as a monomer in the production of polymers with specific functionalities. Its unique structure allows it to participate in polymerization reactions, leading to materials with desirable properties.
  • Chemical Reactivity: The compound can undergo various transformations, including nucleophilic addition and cycloaddition reactions. These reactions are key in the synthesis of complex molecules.

In summary, 2-styryl-1,3-dioxolane offers a wealth of opportunities for research and application in the fields of organic chemistry and materials science. Its intriguing chemical structure and reactivity make it a compound of interest for chemists seeking innovative solutions.

Synonyms
DTXSID2063971
1,3-Dioxolane, 2-(2-phenylethenyl)-
DTXCID9042093
SCHEMBL3257590