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Ethylene sulfite

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Identification
Molecular formula
C2H4O3S
CAS number
3749-67-5
IUPAC name
1,3,2-dioxathiolane 2,2-dioxide
State
State

At room temperature, ethylene sulfite is a liquid.

Melting point (Celsius)
21.00
Melting point (Kelvin)
294.15
Boiling point (Celsius)
136.00
Boiling point (Kelvin)
409.15
General information
Molecular weight
108.10g/mol
Molar mass
108.0990g/mol
Density
1.4056g/cm3
Appearence

Ethylene sulfite is a clear, colorless liquid with a mild aromatic odor.

Comment on solubility

Solubility of 1,3,2-Dioxathiolane 2,2-Dioxide

1,3,2-Dioxathiolane 2,2-dioxide is a fascinating compound with unique solubility properties. Understanding its solubility is crucial for various chemical applications. Here’s a breakdown of key points regarding its solubility:

  • Solvent Compatibility: This compound is typically soluble in polar organic solvents, such as methanol and water, due to the presence of oxygen atoms that can form interactions with solvent molecules.
  • Temperature Dependency: Like many organic compounds, its solubility may increase with temperature. Higher temperatures can enhance molecular motion, leading to better solvation.
  • pH Influence: The solubility of 1,3,2-dioxathiolane 2,2-dioxide can also be influenced by the pH of the solution, especially if any protonation or deprotonation reactions occur, affecting interactions with the solvent.

Furthermore, it is essential to note that the solubility of this compound may exhibit variability depending on the specific conditions and the presence of other solutes in the solution. As a general rule, compounds containing heteroatoms, such as those in 1,3,2-dioxathiolane 2,2-dioxide, often demonstrate enhanced solubility due to their ability to interact with polar solvents.

In summary, the solubility of 1,3,2-dioxathiolane 2,2-dioxide can be described as:

  1. Poorly soluble in non-polar solvents
  2. Soluble in polar solvents
  3. Affected by temperature and pH

By considering these factors, researchers can better predict its behavior in various chemical environments.

Interesting facts

Interesting Facts About 1,3,2-Dioxathiolane 2,2-Dioxide

The compound known as 1,3,2-dioxathiolane 2,2-dioxide is a fascinating subject of study in the field of organic chemistry. Here are some engaging insights about this intriguing compound:

  • Unique Structure: This compound features a dioxathiolane ring, which is characterized by its unusual arrangement of oxygen and sulfur atoms. Such cyclic structures are often associated with diverse reactivity patterns.
  • Reactivity: The presence of both sulfur and oxygen in the molecular framework makes this compound a potential candidate for various chemical reactions, including nucleophilic attacks and oxidation processes.
  • Applications in Organosilicon Chemistry: Due to its unique chemical properties, 1,3,2-dioxathiolane 2,2-dioxide has found potential applications in organosilicon chemistry, contributing to synthesizing innovative materials.
  • Environmental Impact: Compounds like this may play roles in contaminant degradation and environmental remediation, highlighting the importance of studying synthetic organic compounds for ecological applications.
  • Modern Research: Current studies are exploring its use in drug development and agricultural chemistry, showcasing its versatility beyond traditional chemical applications.

In summary, 1,3,2-dioxathiolane 2,2-dioxide is not just a simple compound; it embodies a rich tapestry of chemical interactions, potential applications, and scientific inquiry. Its unique properties and structural characteristics make it a subject of ongoing research and discovery!

Synonyms
1,3,2-Dioxathiolane 2,2-dioxide
1,2-Ethylene sulfate
Glycol sulfate
1,3,2-DIOXATHIOLANE, 2,2-DIOXIDE
Sulfuric acid, cyclic ethylene ester
BRN 1237731
3-01-00-02110 (Beilstein Handbook Reference)
600-809-4
1072-53-3
Ethylenesulfate
Ethylene sulfate
Ethylene glycol, cyclic sulfate
1,3,2-DIOXATHIOLANE-2,2-DIOXIDE
DTXSID3020598
[1,3,2]dioxathiolane 2,2-dioxide
1,3,2-Dioxathiolane,2,2-dioxide; Ethyleneglycol, cyclic sulfate (8CI)
C2H4O4S
ethosulfate
ethylene sulphate
1,3,2??-DIOXATHIOLANE-2,2-DIONE
SCHEMBL52208
DTXCID70598
Ethylene glycol cyclic sulfate
CHEMBL3186939
Tox21_200498
MFCD00221769
NSC526594
AKOS015855774
CS-W007741
FE29776
NSC-526594
1,3,2lambda6-dioxathiolane-2,2-dione
NCGC00248660-01
NCGC00258052-01
AS-20144
CAS-1072-53-3
1,3,2-Dioxathiolane 2,2-dioxide, 98%
D2830
NS00023449
EN300-365581
Q63088203
1,3,2-Dioxathiolane 2,2-dioxide;Ethylene glycol cyclic sulfate;DTD