Skip to main content

2-chloroethyl 2-phenoxyacetate

ADVERTISEMENT
Identification
Molecular formula
C10H11ClO3
CAS number
3763-23-1
IUPAC name
2-chloroethyl 2-phenoxyacetate
State
State
The compound is a liquid at room temperature.
Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
310.00
Boiling point (Kelvin)
583.15
General information
Molecular weight
228.64g/mol
Molar mass
228.6590g/mol
Density
1.2182g/cm3
Appearence

2-chloroethyl 2-phenoxyacetate appears as a colorless to pale yellow liquid. It may have a sweet, ether-like odor due to the presence of the ester functional group.

Comment on solubility

Solubility of 2-chloroethyl 2-phenoxyacetate

2-chloroethyl 2-phenoxyacetate, known for its unique applications, exhibits moderate solubility characteristics in various solvents.

  • Polar Solvents: This compound tends to show reasonable solubility in polar solvents such as ethanol or methanol, likely due to dipole interactions.
  • Non-Polar Solvents: Conversely, it has limited solubility in non-polar solvents, indicating a lack of favorable interactions.
  • Water Solubility: 2-chloroethyl 2-phenoxyacetate displays low solubility in water, often attributed to its hydrophobic aromatic structure.

Overall, understanding the solubility of this compound is crucial, as it influences its bioavailability and potential applications in various fields. As a general rule, it's essential to perform solvent compatibility tests when working with this compound to ensure optimal performance in formulations.

Interesting facts

Interesting Facts about 2-chloroethyl 2-phenoxyacetate

2-chloroethyl 2-phenoxyacetate, also known as an important intermediate in organic synthesis, is noteworthy for a variety of reasons:

  • Use in Pharmaceuticals: This compound is often explored for its potential applications in the pharmaceutical industry, particularly in the synthesis of various medicinal agents. Its structure allows for modifications that can lead to new therapeutic compounds.
  • Agricultural Applications: The phenoxyacetate group can confer herbicidal properties, making it valuable in the development of agricultural chemicals. Compounds with this functional group are often studied for their ability to control weed growth effectively.
  • Synthetic Versatility: The presence of both chloro and phenoxy groups in the molecule makes it a versatile building block in organic synthesis. Chemists appreciate its functionality in creating more complex molecules through various reaction pathways.
  • Research Interest: Scientists are continually examining this compound's reactivity and stability, paving the way for innovative reactions and applications. Research may focus on how altering specific parts of the molecule can yield beneficial properties or applications.
  • Environmental Impact: Like many chemical compounds used in agriculture, understanding its environmental interactions is crucial. Studies often investigate its breakdown products and ecological effects to ensure safe usage.

In summary, 2-chloroethyl 2-phenoxyacetate serves as a fascinating intersection of chemistry, synthesis, and application. Its significance in drug development and agriculture highlights the importance of such compounds in enhancing both human health and food production.

Synonyms
2-Chloroethyl phenoxyacetate
946-88-3
ACETIC ACID, PHENOXY-, 2-CHLOROETHYL ESTER
NSC-7000
2-chloroethyl 2-phenoxyacetate
NSC 7000
BRN 1961643
RV3VUV9ST3
WLN: G2OV1OR
DTXSID40241551
NSC7000
DS-004005
Acetic acid, 2-phenoxy-, 2-chloroethyl ester