2,2,3-Trichlorooxirane

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Identification

Molecular formula
C3H3Cl3O
CAS Number
547-01-9
IUPAC Name
2,2,3-trichlorooxirane
Molecular Weight
145.43g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
compared to other organic liquids, and it will not solidify at standard ambient temperatures.
Synonyms
Trichloroepoxyethane
Interesting facts

Interesting Facts about 2,2,3-Trichlorooxirane

2,2,3-Trichlorooxirane, commonly known as a chlorinated epoxide, is a fascinating compound with various applications in both industrial settings and scientific research. Here are some engaging points about this unique molecule:

  • Structural Significance: This compound belongs to the epoxide family, characterized by a three-membered cyclic ether. The presence of three chlorine atoms attached to the carbon framework makes it particularly noteworthy.
  • Reactivity: The epoxide functional group enhances the reactivity of the molecule, enabling it to participate in various chemical reactions, including ring-opening reactions and nucleophilic substitutions.
  • Applications: 2,2,3-Trichlorooxirane is used as an intermediate in organic synthesis, helping to produce a range of chemical products, including pesticides, pharmaceuticals, and specialty chemicals.
  • Toxicity Considerations: As a chlorinated compound, it’s essential to handle this molecule with care. It poses potential health risks, and its toxicity necessitates proper safety measures during experiments and usage.
  • Environmental Impact: The production and degradation of chlorinated epoxides are subjects of ongoing research due to their potential effects on the environment and human health.

In the words of renowned chemist Linus Pauling, “The best way to have a good idea is to have lots of ideas.” This insight applies to the exploration of compounds like 2,2,3-trichlorooxirane, highlighting the dynamic nature of chemistry and the surprising roles such compounds can play in various fields.

Overall, 2,2,3-trichlorooxirane is a compound that exemplifies the intersection of reactivity, utility, and caution within the broader context of chemical science.

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