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2-Fluoroethyl 2,2-diphenylacetate

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Identification
Molecular formula
C16H15FO2
CAS number
103068-38-4
IUPAC name
2-fluoroethyl 2,2-diphenylacetate
State
State

At room temperature, 2-Fluoroethyl 2,2-diphenylacetate is in a liquid state. It is generally stable under normal conditions and can be handled in standard laboratory environments.

Melting point (Celsius)
-0.50
Melting point (Kelvin)
272.70
Boiling point (Celsius)
305.50
Boiling point (Kelvin)
578.70
General information
Molecular weight
272.32g/mol
Molar mass
272.3150g/mol
Density
1.1260g/cm3
Appearence

2-Fluoroethyl 2,2-diphenylacetate typically appears as a colorless to light yellow liquid. Its appearance may vary slightly depending on its purity and specific storage conditions. It is often characterized by a slightly fruity odor due to the ester functional group present in the compound.

Comment on solubility

Solubility of 2-fluoroethyl 2,2-diphenylacetate

2-fluoroethyl 2,2-diphenylacetate is a fascinating compound when it comes to solubility. Its characteristics can be summarized as follows:

  • Solvent Compatibility: This compound is primarily soluble in organic solvents due to its hydrophobic nature.
  • Polar vs. Non-polar: It demonstrates increased solubility in non-polar solvents like hexane and chloroform, while exhibiting limited solubility in polar solvents such as water.
  • Temperature Effect: Like many organic compounds, its solubility can also be affected by temperature; generally, a rise in temperature increases solubility in organic solvents.

In summary, the solubility characteristics of 2-fluoroethyl 2,2-diphenylacetate make it quite versatile in organic chemistry applications, where understanding the solubility profile is key to effective usage and synthesis.

Interesting facts

Interesting Facts About 2-Fluoroethyl 2,2-Diphenylacetate

2-Fluoroethyl 2,2-diphenylacetate is a fascinating compound that belongs to the category of esters. It showcases a unique combination of functional groups, which provides it with a variety of intriguing properties and potential applications. Here are some noteworthy points about this compound:

  • Structural Highlights: The compound features a fluoroethyl group, which enhances its reactivity and biological profile, alongside a diphenylacetate moiety that contributes to its aromatic characteristics.
  • Applications in Synthesis: Due to its reactivity, 2-fluoroethyl 2,2-diphenylacetate serves as an important intermediate in organic synthesis. It is used to create various complex molecules in pharmaceutical chemistry.
  • Role in Medicinal Chemistry: Compounds containing fluorine often exhibit improved metabolic stability and bioavailability, making them suitable for drug development. This compound could potentially be explored for its therapeutic effects.
  • Environmental Impact: As a derivative of phenylacetate, it is essential for researchers to assess the environmental persistence and toxicity of this compound during its use and disposal, ensuring safety protocols are in place.
  • Chemical Behavior: The presence of the fluorine atom in its structure can affect the electronegativity of the compound, influencing its solubility and interaction with various solvents.
  • Product of Interest: Chemists are continually investigating derivatives of diphenylacetates for their potential in creating new materials with unique electronic and optical properties.

In conclusion, 2-fluoroethyl 2,2-diphenylacetate is not just an ordinary ester; its intriguing structure and reactivity open new avenues in both academic research and industrial applications. The exploration of such compounds can lead to significant advancements in various fields, particularly in medicinal and materials chemistry.

Synonyms
2-Fluoroethyldiphenyl acetate
4242-33-5
ACETIC ACID, DIPHENYL-, 2-FLUOROETHYL ESTER
diphenylacetic acid 2-fluoroethyl ester
2-fluoroethyl diphenylacetate
DTXSID10962468