2,2,3,3-Tetrachlorooxirane
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- Molecular formula
- C2HCl4O
- CAS Number
- 1189-68-4
- IUPAC Name
- 2,2,3,3-tetrachlorooxirane
- Molecular Weight
- 187.83g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.7310g/cm3
- Synonyms
- TETRACHLOROETHYLENE OXIDE
Identification
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.