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Ethyl 13,14-diiodoeicos-13-enoate

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Identification
Molecular formula
C24H44I2O2
CAS number
90347-07-2
IUPAC name
ethyl 13,14-diiododocos-13-enoate
State
State

At room temperature, ethyl 13,14-diiododocos-13-enoate is typically in a liquid state. It is known for being viscous.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
275.50
Boiling point (Kelvin)
548.60
General information
Molecular weight
592.32g/mol
Molar mass
592.3200g/mol
Density
2.0500g/cm3
Appearence

Ethyl 13,14-diiododocos-13-enoate is typically a colorless or slightly yellow viscous liquid. The compound's appearance can vary slightly depending on purity and storage conditions.

Comment on solubility

Solubility of Ethyl 13,14-Diiododocos-13-enoate

The solubility of ethyl 13,14-diiododocos-13-enoate is an intriguing aspect that reflects its chemical structure and interactions with solvents. This compound, featuring both a long carbon chain and multiple iodine substituents, presents a unique case for solubility behavior.

Key Factors Influencing Solubility

  • Hydrophobic Character: The lengthy hydrocarbon tail contributes to its hydrophobic nature, making it less soluble in polar solvents such as water.
  • Iodine Substituents: The presence of iodine atoms can enhance the solubility in organic solvents, particularly non-polar or slightly polar substances.
  • Temperature: Like many organic compounds, solubility may increase with temperature. Heating the solvent can lead to enhanced molecular interaction.

In general, one can expect ethyl 13,14-diiododocos-13-enoate to have limited solubility in water but a more favorable solubility profile in organic solvents such as hexane or chloroform. As stated, "The solubility of a compound is a dance of molecular interactions," highlighting the importance of structure in defining how and where a compound will dissolve.

In summary, while the hydrophobic character is a defining attribute, the unique functional groups in this compound add complexity to its solubility landscape. Understanding these factors is crucial for practical applications and further research.

Interesting facts

Interesting Facts about Ethyl 13,14-Diiododocos-13-enoate

Ethyl 13,14-diiododocos-13-enoate is a unique and intriguing compound with various applications in the field of chemistry and biochemistry. Here are some notable points:

  • Structural Innovation: This compound features a long-chain fatty acid derivative, emphasizing the significance of alkenes and iodine substitution in organic synthesis.
  • Biological Relevance: Fatty acid derivatives like this one play essential roles in biological systems, including the formation of cell membranes and energy storage.
  • Model Compound: Ethyl 13,14-diiododocos-13-enoate serves as a valuable model for studying lipid behavior and metabolism, aiding in the understanding of similar natural compounds.
  • Potential Applications: Due to its structural properties, this compound may have potential uses in pharmaceuticals, agrochemicals, and as an intermediate in the synthesis of more complex molecules.

Research Opportunities

This compound opens doors for various research opportunities, including:

  1. Investigating the effects of iodine substitution on the biological activity of fatty acids.
  2. Exploring the reaction mechanisms involved in the synthesis of similar compounds.
  3. Studying its interaction with biological membranes and potential impacts on cell signaling.

In summary, the exploration of ethyl 13,14-diiododocos-13-enoate contributes to the broader understanding of lipid chemistry and offers numerous paths for scientific inquiry. As scientists continue to unravel the complexities of such compounds, the implications for health, industry, and fundamental research remain significant.

Synonyms
583-87-9
13-Docosenoic acid, 13,14-diiodo-, ethyl ester
DTXSID7073199
NS00033920