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Ethyl 12-fluoro-3-oxododecanoate

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Identification
Molecular formula
C14H25FO3
CAS number
28255-10-7
IUPAC name
ethyl 12-fluoro-3-oxo-dodecanoate
State
State

At room temperature, ethyl 12-fluoro-3-oxododecanoate is typically a liquid.

Melting point (Celsius)
-30.00
Melting point (Kelvin)
243.15
Boiling point (Celsius)
305.00
Boiling point (Kelvin)
578.15
General information
Molecular weight
246.35g/mol
Molar mass
246.3150g/mol
Density
1.0280g/cm3
Appearence

Ethyl 12-fluoro-3-oxododecanoate is typically a colorless to light yellow liquid with a slight pleasant odor, often characteristic of ester compounds.

Comment on solubility

Solubility of Ethyl 12-fluoro-3-oxo-dodecanoate

Ethyl 12-fluoro-3-oxo-dodecanoate, a compound characterized by its unique structure, displays intriguing solubility properties:

  • Polar Nature: The presence of the carbonyl group (C=O) significantly contributes to the compound's ability to interact with polar solvents.
  • Fluorine Substitution: The fluorine atom introduces a level of polarity and can enhance solubility in certain organic solvents.
  • Long Hydrocarbon Chain: The lengthy dodecanoate structure tends to impart hydrophobic characteristics, which can reduce overall solubility in water.
  • Solvent Interaction: Ethyl 12-fluoro-3-oxo-dodecanoate is expected to be more soluble in organic solvents like ethanol, acetone, and chloroform due to favorable interactions with their molecular properties.

As a result, while the compound is likely soluble in various organic solvents, its solubility in water may be limited. This combination of factors illustrates the complexity of solubility in organic compounds, where structure dictates the behavior.

Interesting facts

Exploring Ethyl 12-Fluoro-3-Oxo-Dodecanoate

Ethyl 12-fluoro-3-oxo-dodecanoate is a fascinating compound that holds significance in various fields, including organic synthesis and medicinal chemistry. This compound is an ester derived from dodecanoic acid, making it part of a broader family of fatty acid derivatives.

Key Characteristics

  • Fluorine Substitution: The presence of a fluorine atom in its structure can enhance biological activity and lipophilicity, offering unique properties not found in its non-fluorinated counterparts.
  • Functional Groups: It contains both an ester and a keto group, making it a valuable intermediate in synthetic organic chemistry. These functional groups can be modified, allowing for the creation of a wide range of compounds.
  • Applications: Compounds similar to ethyl 12-fluoro-3-oxo-dodecanoate are often explored for their potential use in pharmaceuticals, agrochemicals, and as chemical building blocks in research.

Uses in Research and Industry

This compound serves as a useful model for understanding the behavior and reactivity of fluorinated compounds. Research has shown that the incorporation of fluorine can significantly alter the chemical properties of molecules, making them more effective in targeted applications.

Conclusion

In conclusion, ethyl 12-fluoro-3-oxo-dodecanoate exemplifies the interesting intersections of organic chemistry and industrial design. With ongoing studies focused on fluorinated molecules, the potential for discovering new applications appears boundless. As we continue to explore these compounds, we uncover both their structural complexities and their practical uses in various sectors.

Synonyms
Ethyl 12-fluoro-3-oxododecanoate
BRN 1787655
Ethyl omega-fluoro-3-oxododecanoate
DODECANOIC ACID, 12-FLUORO-3-OXO-, ETHYL ESTER
352-82-9
DTXSID90188700
4-03-00-01665 (Beilstein Handbook Reference)
DTXCID10111191