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Ethyl 10-fluorodecanoate

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Identification
Molecular formula
C12H23FO2
CAS number
334-79-8
IUPAC name
ethyl 10-fluorodecanoate
State
State

At room temperature, ethyl 10-fluorodecanoate is typically found in a liquid state.

Melting point (Celsius)
-45.00
Melting point (Kelvin)
228.15
Boiling point (Celsius)
259.00
Boiling point (Kelvin)
532.15
General information
Molecular weight
220.31g/mol
Molar mass
220.2900g/mol
Density
0.9647g/cm3
Appearence

Ethyl 10-fluorodecanoate is a colorless liquid with a mild, pleasant odor often used in fragrance and flavor applications. It has an oily consistency and is not soluble in water, but it is soluble in most organic solvents.

Comment on solubility

Solubility of Ethyl 10-Fluorodecanoate

Ethyl 10-fluorodecanoate, with the molecular formula C12H23F O2, exhibits interesting solubility characteristics that are worth discussing. This compound, which is an ester, typically shows varying solubility in different solvents.

Solubility Characteristics

  • Polar Solvents: Ethyl 10-fluorodecanoate is expected to have limited solubility in polar solvents such as water due to its long hydrophobic carbon chain.
  • Non-Polar Solvents: It is more likely to be soluble in non-polar solvents like hexane and chloroform, where it can efficiently interact with the surrounding molecules.
  • Miscibility: The fluorine atom in its structure may influence its miscibility with organic solvents, potentially enhancing solubility under certain conditions.

In essence, the solubility of ethyl 10-fluorodecanoate primarily relies on the polarity of the solvent used. To summarize:

  1. Low solubility in polar solvents (e.g., water).
  2. Higher solubility in non-polar organic solvents.

Understanding these solubility patterns is crucial for applications in various chemical processes and industries.

Interesting facts

Interesting Facts about Ethyl 10-Fluorodecanoate

Ethyl 10-fluorodecanoate is a fascinating compound belonging to the family of fatty acid esters, specifically within the category of fluorinated compounds. This compound features an ethyl group attached to the carboxylic acid derived from decanoic acid, with a fluorine substituent on the 10th carbon. This structure introduces several intriguing aspects:

  • Fluorination Impact: The presence of the fluorine atom can significantly alter the physical and chemical properties of the compound, including volatility and polarity. Fluorinated compounds are known for their unique interactions in biological and environmental systems.
  • Applications: Ethyl 10-fluorodecanoate can have various applications in the fields of organic synthesis, agrochemicals, and pharmaceuticals. It is especially useful in designing fluorinated molecules for drug development.
  • Biological Activity: Compounds like ethyl 10-fluorodecanoate may exhibit interesting biological activities due to the presence of the fluorine atom, making them subjects of study in medicinal chemistry for their potential therapeutic effects.
  • Synthesis Opportunities: Chemists are continually exploring novel synthetic routes to create such compounds, promoting advancements in synthetic organic chemistry and contributing to the development of new methodologies.

In summary, ethyl 10-fluorodecanoate represents a unique intersection of chemistry, biology, and practical application. As scientists delve deeper into the world of fluorinated compounds, the significance of such molecules continues to grow, sparking curiosity and innovation across various scientific disciplines.

Synonyms
Ethyl 10-fluorodecanoate
10-Fluorodecanoic acid ethyl ester
353-03-7
Ethyl 9-fluorononanecarboxylate
Ethyl omega-fluorodecanoate
DECANOIC ACID, 10-FLUORO-, ETHYL ESTER
BRN 1771473
DTXSID20188793
4-02-00-01051 (Beilstein Handbook Reference)
DTXCID80111284