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2-Fluoroethyl 8-fluorooctanoate

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Identification
Molecular formula
C10H18F2O2
CAS number
335-54-8
IUPAC name
2-fluoroethyl 8-fluorooctanoate
State
State

At room temperature, 2-fluoroethyl 8-fluorooctanoate exists as a liquid.

Melting point (Celsius)
-34.00
Melting point (Kelvin)
239.15
Boiling point (Celsius)
214.00
Boiling point (Kelvin)
487.15
General information
Molecular weight
222.26g/mol
Molar mass
222.2620g/mol
Density
1.1140g/cm3
Appearence

2-Fluoroethyl 8-fluorooctanoate is usually a colorless liquid. It may emit a slight odor.

Comment on solubility

Solubility of 2-fluoroethyl 8-fluorooctanoate

2-fluoroethyl 8-fluorooctanoate, a compound that exhibits interesting solubility characteristics, is known for its moderate polar nature due to the presence of both the fluoro group and the ester functional group. Its solubility properties can be summarized as follows:

  • Solvent Compatibility: This compound is more likely to be soluble in polar organic solvents such as ethanol and methanol, while showing lower solubility in nonpolar solvents like hexane.
  • Temperature Influence: Generally, increased temperatures can lead to enhanced solubility. Therefore, heating the solvent may assist in dissolving this compound more effectively.
  • Concentration Effects: At higher concentrations, the solubility may be influenced by intermolecular interactions, possibly leading to saturation limits in certain solvents.

In conclusion, while the solubility of 2-fluoroethyl 8-fluorooctanoate may not be exceedingly high in all solvents, its compatibility with polar solvents opens up opportunities for various applications in chemical processes and formulations. Understanding its solubility profile is crucial for researchers working with this compound.

Interesting facts

Interesting Facts about 2-fluoroethyl 8-fluorooctanoate

2-fluoroethyl 8-fluorooctanoate is a fascinating compound that draws interest from both chemists and those in related fields. Here are some captivating points about this molecule:

  • Fluorination Effects: The introduction of fluorine atoms in organic compounds can significantly alter their reactivity and biological activity. Fluorine can enhance lipophilicity, which is essential in drug development.
  • Behavior in Biological Systems: Due to its structure, 2-fluoroethyl 8-fluorooctanoate has the potential to interact uniquely with biological systems. It may mimic fatty acids, leading to intriguing considerations in pharmacology and biochemistry.
  • Applications: This compound could be utilized in the development of pharmaceuticals or agrochemicals, where the fluorine atoms may contribute to improved efficacy and selectivity.
  • Research Opportunities: The synthesis and study of this compound provide valuable opportunities for exploring the impact of fluorine substitutions in various chemical reactions and mechanisms.
  • Environmental Considerations: As with many fluorinated compounds, understanding the environmental fate and transport of 2-fluoroethyl 8-fluorooctanoate is crucial, especially in the context of developing sustainable practices in chemistry.

In conclusion, the unique properties and potential applications of 2-fluoroethyl 8-fluorooctanoate are just beginning to be explored, making it a compound worth further investigation in the fields of organic chemistry and material science. As the scientific community continues to delve deeper, we may uncover even more intriguing uses and characteristics of this compound.

Synonyms
332-94-5
OCTANOIC ACID, 8-FLUORO-, (2-FLUOROETHYL) ESTER
2'-Fluoroethyl 8-fluorooctanoate
8-Fluorooctanoic acid 2-fluoroethyl ester
2'-Fluoroethyl omega-fluorooctanoate
BRN 1771537
DTXSID20186850