Ethyl 13-cyclopent-2-en-1-yltridecanoate

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Identification

Molecular formula
C20H36O2
CAS Number
93974-54-2
IUPAC Name
ethyl 13-cyclopent-2-en-1-yltridecanoate
Molecular Weight
294.49g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
0.8790g/cm3
Synonyms
Chaulmoogric acid, ethyl ester
Interesting facts

Interesting Facts about Ethyl 13-Cyclopent-2-en-1-yltridecanoate

Ethyl 13-cyclopent-2-en-1-yltridecanoate is a fascinating compound within the realm of organic chemistry, primarily recognized for its unique structural configuration. Here are some engaging aspects to consider:

  • Structural Features: This compound features a cyclopentene moiety, which contributes to its intriguing molecular characteristics. The presence of the tridecanoate side chain adds a linear hydrocarbon component that enhances the compound’s reactivity.
  • Synthetic Applications: Ethyl 13-cyclopent-2-en-1-yltridecanoate plays a role in organic synthesis. Chemists often utilize such esters in the creation of more complex molecules due to their ability to undergo various chemical transformations.
  • Fragrance and Flavor Industry: Esters like this one are commonly found in the fragrance and flavor industry, where they can impart fruity or floral notes to products. The specific cyclopentenyl structure may lead to unique olfactory properties, making it valuable in perfumery.
  • Potential Biological Activity: Compounds with complex structures often exhibit interesting biological activities. Research into similar esters has revealed potential as antimicrobial and antifungal agents, warranting investigations into their medicinal properties.
  • Chirality and Isomerism: The compound's structure may present chiral centers, leading to the possibility of multiple stereoisomers. The study of these isomers is crucial in medicinal chemistry, as different configurations can lead to vastly different biological activities.

*In summary,* ethyl 13-cyclopent-2-en-1-yltridecanoate emerges as an important compound in both academic research and industrial applications. The interplay of its structural features and potential uses makes it a subject of continual interest for chemists and students alike.

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