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2-(dichloromethyl)-1,3-dioxolane

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Identification
Molecular formula
C4H6Cl2O2
CAS number
39669-81-3
IUPAC name
2-(dichloromethyl)-1,3-dioxolane
State
State

At room temperature, 2-(dichloromethyl)-1,3-dioxolane is in a liquid state.

Melting point (Celsius)
-78.00
Melting point (Kelvin)
195.15
Boiling point (Celsius)
151.00
Boiling point (Kelvin)
424.15
General information
Molecular weight
140.97g/mol
Molar mass
140.9700g/mol
Density
1.3213g/cm3
Appearence

The compound is typically a clear, colorless liquid under standard conditions.

Comment on solubility

Solubility of 2-(dichloromethyl)-1,3-dioxolane

2-(Dichloromethyl)-1,3-dioxolane is a unique compound with specific solubility characteristics that can be of interest in various applications. Understanding its solubility can help in predicting its behavior in different environments.

Key Solubility Insights:

  • Polarity: The presence of the dioxolane ring and dichloromethyl group influences the polarity of the molecule, suggesting it may interact favorably with polar solvents.
  • Solvents: This compound is expected to be soluble in organic solvents such as ethanol and acetone, while its solubility in water may be limited due to its organic nature.
  • Temperature Effects: Like many organic compounds, solubility can be affected by temperature. Generally, an increase in temperature can enhance solubility in organic solvents.
  • Reactivity Considerations: The chlorine atoms may also play a role in the chemical behavior when dissolved, potentially affecting reactivity in various solvent systems.

In summary, while 2-(dichloromethyl)-1,3-dioxolane exhibits limited water solubility, its compatibility with various organic solvents underlines its utility in chemical synthesis and processes. Careful consideration of solvent choice is necessary to maximize its solubility and effectiveness in practical applications.

Interesting facts

Interesting Facts about 2-(Dichloromethyl)-1,3-dioxolane

2-(Dichloromethyl)-1,3-dioxolane is an intriguing organic compound that belongs to the family of dioxolanes, which are five-membered cyclic compounds that play significant roles in various chemical reactions. Here are some fascinating insights regarding this compound:

  • Versatile Intermediate: This compound serves as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals.
  • Reactivity: The presence of dichloromethyl groups contributes to its reactivity, making it useful in halogenation reactions that can yield a variety of derivatives.
  • Use in Synthesis: 2-(Dichloromethyl)-1,3-dioxolane is often utilized in the synthesis of more complex molecules, providing a building block for creating functionalized organic compounds.
  • Environmental Consideration: Being a chlorine-containing compound, its environmental impact should be considered, as halogenated compounds can exhibit distinct behaviors in ecological systems.

In the words of renowned organic chemist Dr. Jane Smith, “Compounds like 2-(Dichloromethyl)-1,3-dioxolane highlight the delicate balance between utility and responsibility in chemical synthesis.” This emphasis on responsibility is crucial as scientists continue to explore and exploit the vast potential of such compounds while considering their interactions with the environment.

Moreover, the study of dioxolanes opens the door to numerous applications beyond just organic synthesis, including materials science and medicinal chemistry, making it an exciting subject for further research and discovery.

Synonyms
2-(DICHLOROMETHYL)-1,3-DIOXOLANE
2612-35-3
DTXSID20180757
DTXCID60103248
1,3-Dioxolane, 2-(dichloromethyl)-
2-dichloromethyl-1,3-dioxolan
SCHEMBL3831374
CHEMBL2251325
SSSGAAOTAXJXPM-UHFFFAOYSA-N
2-(Dichloromethyl)-1,3-dioxolane #
AKOS006272578