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2,3-dichloro-1,4-dioxane

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Identification
Molecular formula
C4H6Cl2O2
CAS number
33816-85-0
IUPAC name
(3S)-2,3-dichloro-1,4-dioxane
State
State

At room temperature, 2,3-dichloro-1,4-dioxane is a liquid. Despite being clear, it might take on a slightly yellow hue if impurities are present. It is typically liquid under standard conditions with a relatively low viscosity.

Melting point (Celsius)
-0.95
Melting point (Kelvin)
272.20
Boiling point (Celsius)
173.50
Boiling point (Kelvin)
446.65
General information
Molecular weight
155.99g/mol
Molar mass
155.9920g/mol
Density
1.3847g/cm3
Appearence

2,3-Dichloro-1,4-dioxane is a colorless liquid. It can appear as a clear or slightly yellowish fluid and is often noted for its characteristic ether-like odor.

Comment on solubility

Solubility of (3S)-2,3-dichloro-1,4-dioxane

The solubility of (3S)-2,3-dichloro-1,4-dioxane can be characterized by several key aspects:

  • Polar Nature: Due to the presence of chlorine atoms and the dioxane ring, (3S)-2,3-dichloro-1,4-dioxane is polar, which typically enhances its solubility in polar solvents.
  • Solvent Interactions: This compound is expected to be more soluble in organic solvents such as ethanol or acetone, as well as in water to some extent, given the polar functional groups.
  • Temperature Dependence: Like many organic compounds, its solubility may increase with temperature, allowing for greater molecular mobility and interaction with solvent molecules.
  • Applications: The solubility properties often dictate its utility in various chemical processes, ranging from pharmaceuticals to polymer applications.

In summary, the solubility of (3S)-2,3-dichloro-1,4-dioxane offers interesting opportunities in both research and application, influenced by its molecular characteristics and environmental factors.

Interesting facts

Interesting Facts about (3S)-2,3-Dichloro-1,4-Dioxane

(3S)-2,3-Dichloro-1,4-dioxane is a unique chemical compound that belongs to the dioxane family, characterized by its intriguing structure and properties. Here are some noteworthy aspects of this compound:

  • Synthetic Applications: This compound plays a significant role in organic synthesis, serving as an intermediate in the production of various chemicals.
  • Chlorine Substitution: The presence of chlorine atoms on the dioxane ring enhances its reactivity, making it valuable in substitution reactions.
  • Chirality: Being optically active due to its chiral center at the 3-position offers opportunities for the study and application of stereochemistry.
  • Environmental Impact: Chlorinated compounds are often scrutinized for their environmental impact, making (3S)-2,3-dichloro-1,4-dioxane an interesting subject for discussions on green chemistry.

As a compound with potential applications in drug development and industrial processes, (3S)-2,3-dichloro-1,4-dioxane underscores the importance of understanding chemical behavior for innovation in the field of chemistry. Its intriguing structure coupled with the biological implications of its chlorinated form makes it an exciting topic for both academics and industry professionals.

“The beauty of chemistry lies in the unexpected connections between structure and reactivity.”