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Dioxolane

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Identification
Molecular formula
C4H8O2
CAS number
646-06-0
IUPAC name
2-(1,3-dioxolan-2-yl)-1,3-dioxolane
State
State

At room temperature, dioxolane is a liquid. It is known for being a highly volatile compound.

Melting point (Celsius)
-95.00
Melting point (Kelvin)
178.15
Boiling point (Celsius)
75.90
Boiling point (Kelvin)
349.05
General information
Molecular weight
90.08g/mol
Molar mass
90.0800g/mol
Density
1.0600g/cm3
Appearence

Dioxolane is a clear, colorless liquid with a faint, pleasant odor. Its appearance can be likened to that of common ethers.

Comment on solubility

Solubility of 2-(1,3-dioxolan-2-yl)-1,3-dioxolane

2-(1,3-dioxolan-2-yl)-1,3-dioxolane is a fascinating compound when it comes to its solubility characteristics. The solubility of a compound largely depends on its molecular structure, and this molecule is no exception. Here are some key points to consider:

  • Polarity: Due to the presence of multiple ether functionalities, the compound exhibits a degree of polar character. This polarity often contributes to its solubility in polar solvents.
  • Solvent Compatibility: 2-(1,3-dioxolan-2-yl)-1,3-dioxolane is likely to be soluble in common polar solvents such as water, alcohols, and acetonitrile. Conversely, its solubility in non-polar solvents may be limited.
  • Hydrogen Bonding: The structure allows for potential hydrogen bonding, which enhances solubility in polar environments. This is particularly important when considering interactions with solvent molecules.
  • Temperature Effects: Like many chemical compounds, solubility can be temperature-dependent. An increase in temperature often leads to higher solubility for many solutes.

As a general rule, compounds with significant functional groups promoting solubility will fare better in interacting with solvents that share similar properties. In summary, the solubility of 2-(1,3-dioxolan-2-yl)-1,3-dioxolane indicates that it would behave well in aqueous or polar conditions, but caution should be taken when examining its behavior in a non-polar solvent environment.

Interesting facts

Interesting Facts about 2-(1,3-dioxolan-2-yl)-1,3-dioxolane

2-(1,3-dioxolan-2-yl)-1,3-dioxolane, often referred to in the scientific community as a fascinating cyclic organic compound, presents a unique structure with multiple dioxolane rings. Here are some intriguing aspects of this compound:

  • Structural Complexity: The presence of two fused dioxolane rings contributes significantly to its reactivity and potential applications in organic synthesis.
  • Solvent Properties: This compound has been studied for its potential as a solvent or reaction medium due to its unique polarity and ability to stabilize charged intermediates.
  • Application in Green Chemistry: Dioxolane derivatives, including this compound, are noteworthy for their roles as environmentally friendly solvents and reactants in green chemistry initiatives, aligning with sustainable practices.
  • Synthetic Versatility: The multifunctionality of the dioxolane moiety allows for various chemical transformations, making it a valuable building block in the synthesis of pharmaceuticals and agrochemicals.
  • Intriguing Reactivity: Due to its structure, 2-(1,3-dioxolan-2-yl)-1,3-dioxolane might participate in unique reactions, such as ring-opening or polymerization, encouraging innovative research avenues.

In summary, the study of 2-(1,3-dioxolan-2-yl)-1,3-dioxolane offers a promising look into the world of dioxolane compounds, where the balance between structure and reactivity can lead to advancements in organic synthesis and sustainable chemistry. As a chemist, one can appreciate how the intricate interplay of rings and functional groups provides both challenges and opportunities for exploration.

Synonyms
2,2'-BIS(1,3-DIOXOLANE)
2-(1,3-dioxolan-2-yl)-1,3-dioxolane
6705-89-1
2,2'-Bis[1,3-dioxolane]
2,2'-Bi-1,3-dioxolane
2,2'-Bi
bis(1,3-dioxolan-2-yl)
Bi-1,3-dioxacyclopentyl-(2)
SCHEMBL3069575
DTXSID60217339
AKOS006295793
Ethanedial, cyclic 1,1:2,2-bis(1,2-ethanediyl acetal)