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2-Fluoroethyl cinnamate

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Identification
Molecular formula
C11H11FO2
CAS number
943-87-9
IUPAC name
2-fluoroethyl 3-phenylprop-2-enoate
State
State

At room temperature, 2-Fluoroethyl cinnamate is a liquid. It is not a solid or a gas at room temperature and pressure, maintaining a stable liquid state under normal conditions.

Melting point (Celsius)
-35.00
Melting point (Kelvin)
238.15
Boiling point (Celsius)
281.00
Boiling point (Kelvin)
554.15
General information
Molecular weight
194.20g/mol
Molar mass
194.1920g/mol
Density
1.0960g/cm3
Appearence

2-Fluoroethyl cinnamate is a pale yellow liquid. It generally appears clear and is noted for its characteristic aromatic odor that resembles a mixture of fruity and floral scents. It's typically handled in small amounts as it is used mainly in the field of synthetic organic chemistry and fragrance industries.

Comment on solubility

Solubility of 2-fluoroethyl 3-phenylprop-2-enoate

2-fluoroethyl 3-phenylprop-2-enoate exhibits intriguing solubility characteristics that are influenced by its molecular structure. As a compound composed of both polar and nonpolar functional groups, its solubility can be analyzed as follows:

  • Polar Characteristics: The presence of the fluoroethyl group contributes to a certain level of polarity, which can enhance solubility in polar solvents such as:
    • Water
    • Methanol
    • Ethanol
  • Nonpolar Characteristics: Conversely, the phenyl group from the 3-phenylprop-2-enoate moiety offers significant hydrophobic character, promoting solubility in organic solvents like:
    • Hexane
    • Chloroform
    • Acetone

This dual nature indicates that 2-fluoroethyl 3-phenylprop-2-enoate can be reasonably soluble in a variety of solvents depending on their polarity. As a general trend, compounds with similar polarities tend to dissolve better. Therefore, when considering this compound’s solubility, it is essential to consider the solvent environment, as it significantly influences its overall solubility profile. In summary, 2-fluoroethyl 3-phenylprop-2-enoate is likely to be more soluble in polar aprotic solvents than in purely nonpolar environments.

Interesting facts

Interesting Facts About 2-Fluoroethyl 3-phenylprop-2-enoate

2-Fluoroethyl 3-phenylprop-2-enoate is a fascinating compound that combines unique features of both fluorinated compounds and unsaturated esters. Here are some intriguing facts that highlight its significance in various fields:

  • Fluorine's Influence: The presence of fluorine in this compound can enhance its reactivity and stability. Fluorinated compounds often exhibit properties that differ significantly from their non-fluorinated counterparts, making them valuable in pharmaceuticals and agrochemicals.
  • Versatile Applications: Compounds like 2-fluoroethyl 3-phenylprop-2-enoate are often used in organic synthesis processes. They can act as intermediates in the production of complex molecules, contributing to advancements in material science and medicinal chemistry.
  • Radical Reactions: The unsaturated nature of the 3-phenylprop-2-enoate group allows it to participate in various radical reactions, paving the way for the development of novel organic structures.
  • Research Potential: As scientists continue to explore the properties of this compound, its potential applications in drug delivery systems and as a building block for new materials are being investigated. This opens up new avenues for research and development.
  • Structure-Activity Relationship: Understanding how the structure of 2-fluoroethyl 3-phenylprop-2-enoate affects its biological activity can be crucial in drug design, particularly in optimizing the efficacy and reducing side effects of pharmaceutical agents.

This compound exemplifies how the inclusion of specific functional groups can tailor the properties of organic molecules. Its unique structure not only serves in practical applications but also sparks curiosity and encourages ongoing research in the field of organic chemistry.