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Ethyl 9-fluorononanoate

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Identification
Molecular formula
C11H21FO2
CAS number
88230-33-3
IUPAC name
ethyl 9-fluorononanoate
State
State

At room temperature, ethyl 9-fluorononanoate is typically in a liquid state due to its relatively low melting point and moderate boiling point for an alkyl ester.

Melting point (Celsius)
-63.00
Melting point (Kelvin)
210.20
Boiling point (Celsius)
251.50
Boiling point (Kelvin)
524.60
General information
Molecular weight
218.30g/mol
Molar mass
218.2970g/mol
Density
0.9527g/cm3
Appearence

Ethyl 9-fluorononanoate typically appears as a clear, colorless to pale yellow liquid. It may have a slightly fruity or ester-like odor common to similar alkyl esters.

Comment on solubility

Solubility of Ethyl 9-Fluorononanoate

Ethyl 9-fluorononanoate is a compound that exhibits interesting solubility properties, which can be influenced by its unique structure. Understanding its solubility is crucial for various applications, especially in organic synthesis and pharmaceuticals.

Key Solubility Characteristics

  • Solvent Compatibility: Ethyl 9-fluorononanoate is generally soluble in organic solvents such as ethyl acetate and dichloromethane, owing to its non-polar characteristics.
  • Water Solubility: The presence of the ethyl group contributes to its overall hydrophobic nature, making it only sparingly soluble in water.
  • Temperature Influence: Like many organic esters, increasing temperature may enhance its solubility in organic solvents, while potentially decreasing solubility in water.

In summary, the solubility of ethyl 9-fluorononanoate can be described as primarily soluble in organic solvents but limited in aqueous environments, influenced significantly by its molecular structure and environmental conditions. Understanding these parameters is vital for its utilization in various chemical processes.

Interesting facts

Interesting Facts about Ethyl 9-Fluorononanoate

Ethyl 9-fluorononanoate is a fascinating compound that showcases the intriguing world of organic chemistry. Here are some notable aspects of this compound:

  • Fluorinated Compounds: The presence of a fluorine atom in ethyl 9-fluorononanoate significantly impacts its chemical properties. Fluorinated compounds are often more stable, and this stability can enhance their use in various applications.
  • Flavor and Fragrance: Compounds like ethyl 9-fluorononanoate and other esters have gained attention in the food industry for their potential use as flavoring agents. The unique structure can contribute to fruity or floral scents, making it valuable in the fragrance industry as well.
  • Biological Activity: There is increasing interest in the biological effects of fluorine-containing compounds. Research indicates that fluorinated esters can exhibit interesting pharmacological properties, making them candidates for drug discovery.
  • Applications in Synthesis: Ethyl 9-fluorononanoate can serve as an important intermediate in organic synthesis, particularly in developing more complex structures due to its reactive sites.
  • The Role of Carbon Chains: The nonanoate variant refers to a 9-carbon chain which may play a role in altering how the compound interacts with other molecules, especially in biochemical systems.

In summary, ethyl 9-fluorononanoate not only exemplifies the complexities of organic chemistry but also underlines the importance of fluorine in enhancing the properties and functionalities of chemical compounds. As research continues to unfold, who knows what new applications we may discover for this remarkable molecule?

Synonyms
Ethyl 9-fluorononanoate
462-68-0
NONANOIC ACID, 9-FLUORO-, ETHYL ESTER
Ethyl omega-fluorononanoate
BRN 1705944
SCHEMBL21233585
DTXSID10196766