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2,2,3,3-Tetrachlorooxirane

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Identification
Molecular formula
C2HCl4O
CAS number
1189-68-4
IUPAC name
2,2,3,3-tetrachlorooxirane
State
State
This compound is generally in a liquid state at room temperature, typically clear to pale yellow.
Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
139.00
Boiling point (Kelvin)
412.15
General information
Molecular weight
187.83g/mol
Molar mass
187.8330g/mol
Density
1.7310g/cm3
Appearence

2,2,3,3-Tetrachlorooxirane is a colorless or pale yellow liquid. It is important to handle it with care due to its reactive nature and potential as a halogenated epoxide.

Comment on solubility

Solubility of 2,2,3,3-Tetrachlorooxirane

2,2,3,3-Tetrachlorooxirane, known for its distinct structure, exhibits some interesting solubility characteristics. Understanding its solubility is pivotal in various chemical applications and reactions.

General Solubility Profile:

  • Polar Solvents: It shows decent solubility in polar solvents, such as water, due to the presence of chlorine atoms, which enhance its interactions through dipole-dipole moments.
  • Non-Polar Solvents: Conversely, it is more soluble in non-polar solvents like hexane or benzene, owing to its hydrophobic characteristics.
  • Effect of Temperature: Generally, an increase in temperature may lead to enhanced solubility for many organic compounds, and 2,2,3,3-tetrachlorooxirane is no exception.

Key Considerations:

When working with 2,2,3,3-tetrachlorooxirane, consider the following:

  • Always assess the compatibility of solvents to ensure effective dissolution.
  • Be aware of its potential toxicity and handle with appropriate safety measures.
  • Due to its chemical structure, 2,2,3,3-tetrachlorooxirane can engage in various chemical reactions, impacting its solubility further.

In conclusion, 2,2,3,3-tetrachlorooxirane's solubility can be nuanced and is a fundamental aspect influencing its application in chemical research and industrial processes.

Interesting facts

Interesting Facts about 2,2,3,3-Tetrachlorooxirane

2,2,3,3-Tetrachlorooxirane, often regarded as a significant compound in organic chemistry, is notable for its unique structure and properties. This compound belongs to a family of cyclic ethers, specifically epoxides, which play a crucial role in various chemical reactions. Below are some fascinating aspects of 2,2,3,3-tetrachlorooxirane:

  • Chemical Reactivity: The presence of multiple chlorine substituents drastically alters the reactivity profile of this compound, making it an interesting subject for study in environmental and synthetic chemistry.
  • Applications: It finds use in the synthesis of other chemicals, particularly as an intermediate in the production of chlorinated compounds, which are significant in various industrial processes.
  • Environmental Impact: As a chlorinated compound, it poses potential environmental risks, including persistence in the environment and bioaccumulation, a topic of interest for chemists focusing on green chemistry and sustainability.
  • Structural Characteristics: The epoxide functional group in its structure allows for ring-opening reactions, which are pivotal in creating more complex molecular architectures.
  • Historical Significance: Its discovery marked a notable advancement in the field of synthetic organic chemistry, demonstrating how halogenation can affect molecular stability and reactivity.

As a compound that encapsulates both the potential for utility and the need for careful handling, 2,2,3,3-tetrachlorooxirane serves as a prime example of the dual nature of synthetic chemicals in modern research.

Synonyms
TETRACHLOROETHYLENE OXIDE
Tetrachlorooxirane
2,2,3,3-tetrachlorooxirane
16650-10-5
2PJ36AO63Q
PCEO
Epoxyperchlorovinyl
Tetrachloroepoxyethane
Oxirane, tetrachloro-
Ethane, tetrachloroepoxy-
BRN 0104771
UNII-2PJ36AO63Q
tetrachloroxirane
5-17-01-00009 (Beilstein Handbook Reference)
SCHEMBL5945078
DTXSID60168115
AKOS006277380
Q27255418