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2-Fluoroethyl 2-(4-methoxyphenyl)acetate

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Identification
Molecular formula
C11H13FO3
CAS number
367-20-8
IUPAC name
2-fluoroethyl 2-(4-methoxyphenyl)acetate
State
State

At room temperature, this compound is found as a liquid. It remains stable under standard atmospheric conditions.

Melting point (Celsius)
-30.00
Melting point (Kelvin)
243.15
Boiling point (Celsius)
235.50
Boiling point (Kelvin)
508.65
General information
Molecular weight
212.21g/mol
Molar mass
212.2140g/mol
Density
1.1442g/cm3
Appearence

2-Fluoroethyl 2-(4-methoxyphenyl)acetate typically appears as a colorless liquid at room temperature.

Comment on solubility

Solubility of 2-fluoroethyl 2-(4-methoxyphenyl)acetate

The solubility of 2-fluoroethyl 2-(4-methoxyphenyl)acetate can be influenced by a variety of factors, including temperature, the presence of solvents, and the structural properties of the compound itself. Specific insights into its solubility can be summarized as follows:

  • Polarity: The presence of the fluoro group and methoxy group enhances the polarity of the ester, often leading to improved solubility in polar solvents.
  • Solvent Choice: It is expected to be soluble in a range of organic solvents such as ethanol, methanol, and acetone, while being less soluble in non-polar solvents like hexane.
  • Temperature Dependency: Like many esters, the solubility may increase with temperature, allowing more dissolution in the solvent.

Overall, while the specific solubility values may not be readily available, the structural features suggest it is likely to have moderate to good solubility in appropriate organic solvents. Understanding its solubility can aid in applications such as synthesis or formulation within various chemical contexts.

Interesting facts

Interesting Facts About 2-Fluoroethyl 2-(4-methoxyphenyl)acetate

2-Fluoroethyl 2-(4-methoxyphenyl)acetate is a fascinating compound that often piques the interest of chemists and students alike. It belongs to a class of chemicals known as esters, which are derived from organic acids and alcohols. Here are some compelling aspects to consider:

  • Unique Functional Group: This compound features a fluoroethyl group, which introduces unique properties related to fluoroalkyl chemistry. Fluorine atoms can significantly impact the reactivity and stability of the molecules they are attached to.
  • Pharmacological Potential: The presence of the methoxyphenyl group opens up intriguing possibilities in medicinal chemistry. Such structures are often explored for applications in drug development, potentially leading to new therapeutic agents.
  • Synthetic Versatility: 2-Fluoroethyl 2-(4-methoxyphenyl)acetate can serve as an important intermediate in organic synthesis. Its reactivity allows chemists to build more complex molecules, making it a valuable tool in the arsenal of synthetic organic chemists.
  • Environmental Considerations: The incorporation of fluorine in organic compounds is notable because it may enhance the stability of the molecule against environmental degradation, raising questions in both ecological chemistry and sustainability.
  • Reactivity Patterns: The compound can undergo various chemical reactions, including nucleophilic substitutions and acylations, making it an interesting substrate for exploration in advanced organic reactions.

In summary, 2-fluoroethyl 2-(4-methoxyphenyl)acetate is more than just a chemical name; it represents a convergence of synthetic versatility, pharmacological potential, and environmental implications, embodying the challenges and excitement intrinsic to the field of organic chemistry.

Synonyms
2-Fluoroethyl (4-methoxyphenyl)acetate
4242-37-9
(p-Methoxyphenyl)acetic acid 2-fluoroethyl ester
BRN 3051904
ACETIC ACID, (p-METHOXYPHENYL)-, 2-FLUOROETHYL ESTER
DTXSID50195213
DTXCID60117704