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2,2,3-Trichlorooxirane

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Identification
Molecular formula
C3H3Cl3O
CAS number
547-01-9
IUPAC name
2,2,3-trichlorooxirane
State
State

At room temperature, 2,2,3-Trichlorooxirane is a liquid. The presence of multiple chlorine atoms gives it a relatively high density compared to other organic liquids, and it will not solidify at standard ambient temperatures.

Melting point (Celsius)
-6.30
Melting point (Kelvin)
266.85
Boiling point (Celsius)
152.10
Boiling point (Kelvin)
425.25
General information
Molecular weight
145.43g/mol
Molar mass
145.4310g/mol
Density
1.5724g/cm3
Appearence

2,2,3-Trichlorooxirane typically appears as a colorless liquid with a pungent odor. It is an epoxide compound characterized by the presence of three chlorine atoms, contributing to its density and reactivity. In its pure form, it may be sensitive to light and can decompose upon exposure to heat or strong bases, leading to a loss of clarity and potential discoloration.

Comment on solubility

Solubility of 2,2,3-Trichlorooxirane

2,2,3-Trichlorooxirane, commonly known for its use in various chemical syntheses, exhibits noteworthy solubility characteristics that can influence its applications. Understanding the solubility of this compound is crucial for effectively utilizing it in practical scenarios.

Key Points about Solubility:

  • Polar Nature: The presence of multiple chlorine atoms introduces significant polarity, which enhances its solubility in polar solvents.
  • Solvent Compatibility: It tends to dissolve well in common organic solvents such as acetonitrile, acetone, and alcohols, contributing to its versatility in chemical reactions.
  • Water Solubility: While 2,2,3-trichlorooxirane is primarily insoluble in water, its significant density and structure allow for a degree of interaction with aqueous environments.
  • Concentration Impact: The solubility is also affected by temperature and concentration, with higher temperatures often leading to increased solubility in organic solvents.

In summary, the solubility profile of 2,2,3-trichlorooxirane is primarily influenced by its molecular structure and the nature of the solvent used. Understanding these factors is essential for chemists in optimizing reaction conditions and achieving desired outcomes in their work.

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.

Synonyms
Trichloroepoxyethane
Trichloroethylene epoxide
2,2,3-trichlorooxirane
Trichloro-oxirane
Trichloroethylene oxide
1,1,2-Trichloroepoxyethane
16967-79-6
Epoxy-1,1,2-trichloroethane
TRICHLOROOXIRANE
DXK2817N87
CHEBI:28888
DTXSID80937663
DTXCID101366220
Oxirane, trichloro-
TCE epoxide
TCEO
Ethane, trichloroepoxy-
UNII-DXK2817N87
2,2,3-trichloro-oxi-rane
SCHEMBL3842853
CMMXCVYESRODNH-UHFFFAOYSA-N
AKOS015951110
ETHANE, 1,1,2-TRICHLORO-1,2-EPOXY-
Q27103944