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Methyl 11-(3-pentyloxiran-2-yl)undec-9-enoate

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Identification
Molecular formula
C19H34O3
CAS number
Not available
IUPAC name
methyl 11-(3-pentyloxiran-2-yl)undec-9-enoate
State
State

At room temperature, Methyl 11-(3-pentyloxiran-2-yl)undec-9-enoate is a liquid. It remains stable in this state under normal conditions used in a laboratory or industrial setting.

Melting point (Celsius)
-40.00
Melting point (Kelvin)
233.15
Boiling point (Celsius)
310.50
Boiling point (Kelvin)
583.65
General information
Molecular weight
296.47g/mol
Molar mass
296.4680g/mol
Density
0.9217g/cm3
Appearence

Methyl 11-(3-pentyloxiran-2-yl)undec-9-enoate is typically a clear and colorless liquid. Its liquid state makes it easy to handle and measure. The compound does not have a strong odor and is consistent with other esters in its viscosity.

Comment on solubility

Solubility of Methyl 11-(3-pentyloxiran-2-yl)undec-9-enoate

Methyl 11-(3-pentyloxiran-2-yl)undec-9-enoate, with the chemical formula C19H34O3, showcases intriguing solubility characteristics. Generally, the solubility of organic compounds, especially esters, can be significantly influenced by their molecular structure and functional groups.

Factors Affecting Solubility

  • Hydrophobic vs. Hydrophilic Balance: The presence of long hydrophobic hydrocarbon chains often leads to lower solubility in polar solvents such as water, while promoting higher solubility in non-polar solvents like hexane.
  • Functional Groups: The ester functional group in methyl 11-(3-pentyloxiran-2-yl)undec-9-enoate typically enhances solubility in organic solvents, allowing for better interaction with other similar compounds.
  • Chemical Structure: The incorporation of oxirane (epoxide) rings adds complexity, which may influence solubility through steric hindrance and the nature of interactions with the solvent.

In conclusion, while methyl 11-(3-pentyloxiran-2-yl)undec-9-enoate may exhibit limited solubility in aqueous environments, it is expected to dissolve well in various organic solvents. This behavior showcases the dynamic interplay between molecular structure and solubility, emphasizing the broad range of interactions that compounds can experience in different mediums.

Interesting facts

Interesting Facts about Methyl 11-(3-pentyloxiran-2-yl)undec-9-enoate

Methyl 11-(3-pentyloxiran-2-yl)undec-9-enoate is a fascinating compound that belongs to the family of esters, which are widely recognized for their unique aromas and flavors. Here are some interesting insights into this compound:

  • Versatile Applications: This compound's ester functionality can make it an excellent candidate for use in the production of fragrances, flavors, and agrochemicals, enhancing consumer products and agricultural formulations.
  • Epoxy Groups: The presence of an oxirane or epoxide group provides interesting chemical reactivity, making it valuable for synthetic organic chemistry. This feature allows for various reactions, including ring-opening, which can lead to new compounds with diverse applications.
  • Chain Length Variation: The undec-9-enoate moiety indicates that the compound has a long carbon chain, which can affect its physical properties and functional applications while also influencing its biological activity.
  • Biological Activity: Many esters have shown biological activity, such as antimicrobial or antifungal effects. The unique combination of structural elements in methyl 11-(3-pentyloxiran-2-yl)undec-9-enoate may hint at potential therapeutic uses, warranting further exploration.
  • Research Potential: This compound can serve as a promising precursor in organic synthesis. Researchers could explore various transformations, potentially leading to the discovery of novel compounds with beneficial properties.

In summary, methyl 11-(3-pentyloxiran-2-yl)undec-9-enoate is not just an ordinary ester; its intriguing structure offers various possibilities in both academic and industrial chemistry. Further studies could unlock its potential and unveil new applications.

Synonyms
(+/-)-cis-12,13-Epoxy-9(Z)-octadecenoicacidmethylester
(+)-[12S,13R]-EPOXY-CIS-9-OCTADECENOIC ACID METHYL ESTER
methyl 12,13-epoxy-9-octadecenoate