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1,2-Dichloro-1-methylsulfonyl-ethylene

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Identification
Molecular formula
C3H4Cl2O2S
CAS number
1746-01-6
IUPAC name
1,2-dichloro-1-methylsulfonyl-ethylene
State
State

At room temperature, 1,2-Dichloro-1-methylsulfonyl-ethylene is a liquid. It is typically handled in controlled environments to prevent evaporation due to its volatility.

Melting point (Celsius)
1.50
Melting point (Kelvin)
274.65
Boiling point (Celsius)
172.00
Boiling point (Kelvin)
445.15
General information
Molecular weight
177.03g/mol
Molar mass
177.0270g/mol
Density
1.3578g/cm3
Appearence

1,2-Dichloro-1-methylsulfonyl-ethylene is a colorless to pale yellow liquid with a distinct odor. It typically appears clear and is available in various levels of purity depending on its industrial or laboratory use.

Comment on solubility

Solubility of 1,2-Dichloro-1-methylsulfonyl-ethylene

1,2-Dichloro-1-methylsulfonyl-ethylene, with the chemical formula C3H4Cl2O2S, exhibits notable characteristics regarding its solubility:

  • Polar Solvent Compatibility: This compound is likely to show solubility in polar solvents due to the presence of the sulfonyl group (-SO2), which enhances its interaction with polar molecules.
  • Limited Solubility in Nonpolar Solvents: Because of its polar functional groups, its solubility in nonpolar solvents (like hexane or toluene) is expected to be quite low.
  • Hydrophobic and Hydrophilic Balance: The dichloro groups may impart some hydrophobic character, influencing its overall solubility behavior in various media.

In summary, 1,2-dichloro-1-methylsulfonyl-ethylene demonstrates selective solubility predominantly in polar environments, making it an interesting compound for various chemical applications. Researchers often emphasize understanding such solubility characteristics as they play a crucial role in formulations and reactivity.

Interesting facts

Interesting Facts About 1,2-Dichloro-1-methylsulfonyl-ethylene

1,2-Dichloro-1-methylsulfonyl-ethylene is a fascinating compound that plays an intriguing role in various fields of chemistry and material science. Here are some compelling points that reveal its significance:

  • Versatile Intermediate: This compound is often utilized as an intermediate in organic synthesis, providing a building block for the formation of more complex molecules.
  • Reactive Nature: It contains both chlorine and sulfonyl functional groups, making it highly reactive. This property allows it to engage in a variety of chemical reactions, such as nucleophilic substitutions and coupling reactions.
  • Applications in Agrochemicals: One of the notable applications of this compound is in the agrochemical industry. It is studied for its potential use as a herbicide, contributing to the development of more effective weed control methods.
  • Insight into Structure-Activity Relationships: The presence of the sulfonyl group provides valuable insights into structure-activity relationships in medicinal chemistry, helping researchers design more efficient pharmaceuticals.
  • Environmental Considerations: As with many synthetic compounds, understanding the environmental impact of 1,2-dichloro-1-methylsulfonyl-ethylene is crucial. Research into its degradation pathways is ongoing to ensure that its use does not pose long-term ecological risks.

This compound illustrates the complexity and depth of synthetic organic chemistry, where small structural modifications can lead to significant changes in chemical behavior and applications. As tools and techniques continue to advance, the exploration of such compounds opens up new avenues for innovation in science.

Synonyms
1,2-Dichloro-1-(methylsulfonyl)ethene
2700-89-2
SCHEMBL11116682
DTXSID201031109