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2-(4-Chlorophenyl)-1,3-oxathiolane

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Identification
Molecular formula
C9H9ClOS
CAS number
27314-13-2
IUPAC name
2-(4-chlorophenyl)-1,3-oxathiolane
State
State

At room temperature, 2-(4-Chlorophenyl)-1,3-oxathiolane is usually found in a solid state. The compound remains stable under typical conditions and should be handled with care to avoid exposure to moisture and humidity which could impact its stability and purity.

Melting point (Celsius)
56.00
Melting point (Kelvin)
329.00
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.00
General information
Molecular weight
204.68g/mol
Molar mass
204.6800g/mol
Density
1.3600g/cm3
Appearence

2-(4-Chlorophenyl)-1,3-oxathiolane typically appears as a solid compound. It may manifest in a crystalline form and has a clear to light yellow coloration depending on its purity and other factors related to its preparation.

Comment on solubility

Solubility of 2-(4-chlorophenyl)-1,3-oxathiolane

The solubility of 2-(4-chlorophenyl)-1,3-oxathiolane can be characterized as follows:

  • Polarity Considerations: Being an oxathiolane, the compound contains both sulfur and oxygen, contributing to its polar characteristics.
  • Solvent Interactions: Its solubility may vary significantly depending on the solvent used. For instance, it is likely to be more soluble in polar solvents such as ethanol or dimethyl sulfoxide (DMSO) than in non-polar solvents.
  • Hydrogen Bonding: The presence of heteroatoms suggests potential for hydrogen bonding, which can enhance solubility in polar solvents.
  • Temperature Effects: Like many organic compounds, the solubility of 2-(4-chlorophenyl)-1,3-oxathiolane may increase with rising temperatures due to greater molecular motion.
  • Concentration Factors: It might exhibit limited solubility at lower concentrations, becoming more soluble as the concentration increases, a typical behavior for many organic compounds.

In summary, while specific solubility values may not be readily available, understanding the intermolecular interactions and environmental conditions can provide valuable insights into the solubility behavior of 2-(4-chlorophenyl)-1,3-oxathiolane.

Interesting facts

Interesting Facts about 2-(4-Chlorophenyl)-1,3-oxathiolane

2-(4-Chlorophenyl)-1,3-oxathiolane is a fascinating compound that showcases the intricate world of organic chemistry and its applications. Here are some noteworthy aspects of this compound:

  • Structure and Function: The unique structure of 2-(4-chlorophenyl)-1,3-oxathiolane features an oxathiolane ring—a five-membered heterocyclic compound that includes both sulfur and oxygen. This arrangement contributes to its distinctive chemical behavior and makes it an intriguing subject for study in medicinal chemistry.
  • Biological Activity: Compounds containing oxathiolane structures have been investigated for their potential biological activities. Research has indicated that oxathiolanes may exhibit antiviral and anti-inflammatory properties, making them valuable for drug development.
  • Applications in Pharmaceuticals: The presence of the 4-chlorophenyl group enhances the compound's lipophilicity, which can influence its absorption and distribution in biological systems. This characteristic is crucial in the design of pharmaceuticals, allowing chemists to tailor compounds for specific therapeutic targets.
  • Research Significance: The study of compounds like 2-(4-chlorophenyl)-1,3-oxathiolane contributes fundamentally to our understanding of chemical interactions, synthetic pathways, and the development of innovative drugs that can combat various diseases.
  • Environmental Considerations: As with many synthetic compounds, understanding the environmental impact and the behavior of 2-(4-chlorophenyl)-1,3-oxathiolane is vital. Proper disposal and handling procedures are essential to minimize ecological risks, especially given its potential biological activity.

In conclusion, 2-(4-chlorophenyl)-1,3-oxathiolane is not just a chemical entity but a potential key player in the advancement of medicinal chemistry. Its intriguing characteristics and applications highlight the importance of continued research in this field.

Synonyms
2-(4-chlorophenyl)-1,3-oxathiolane
22391-05-5
DTXSID80945046
BRN 0141805
2-(p-Chlorophenyl)-1,3-oxathiolane
1,3-OXATHIOLANE, 2-(p-CHLOROPHENYL)-
RefChem:1061194
CHEMBL5278982
DTXCID801373373
MFCD01710281
AKOS024321214
A1-25788