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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
State
State

At room temperature, this compound is a liquid. It is used in applications where its unique chemical properties as an ester are required.

Melting point (Celsius)
-30.00
Melting point (Kelvin)
243.00
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.00
General information
Molecular weight
294.49g/mol
Molar mass
294.4870g/mol
Density
0.8790g/cm3
Appearence

Ethyl 13-cyclopent-2-en-1-yltridecanoate is typically a colorless to light yellow liquid. It has a distinctive odor that is commonly found in various chemical esters.

Comment on solubility

Solubility of Ethyl 13-Cyclopent-2-en-1-yltridecanoate (C20H36O2)

Ethyl 13-cyclopent-2-en-1-yltridecanoate is a complex ester that exhibits unique solubility characteristics due to its molecular structure. Understanding its solubility behavior is essential for various applications in chemistry and related fields.

Key Points on Solubility:

  • Polar vs Nonpolar: This compound is primarily nonpolar owing to its long hydrocarbon chain, which significantly influences its solubility.
  • Solvent Compatibility: Ethyl 13-cyclopent-2-en-1-yltridecanoate is likely to be soluble in organic solvents such as:
    • Hexane
    • Ether
    • Chloroform
  • Poor Water Solubility: Due to its nonpolar characteristics, it exhibits poor solubility in water, which is a common trait for many esters of this nature.
  • Temperature Dependence: Like many organic compounds, its solubility can vary with temperature, likely increasing at elevated temperatures.

In summary, the solubility of ethyl 13-cyclopent-2-en-1-yltridecanoate is predominantly influenced by its long hydrophobic chain, leading to excellent solubility in nonpolar solvents and limited solubility in polar solvents such as water. Understanding these solubility dynamics is crucial for practical applications in chemical formulation and synthesis.

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.

Synonyms
Chaulmoogric acid, ethyl ester
Chaulmoogric acid ethyl ester
ethyl 13-cyclopent-2-en-1-yltridecanoate
623-32-5
NSC38010
Spectrum_001411
Spectrum2_000511
Spectrum3_001357
Spectrum4_000118
Spectrum5_000724
BSPBio_003173
KBioGR_000476
KBioSS_001891
SPECTRUM310017
DivK1c_000627
SPBio_000461
CHEMBL1329881
HMS501P09
KBio1_000627
KBio2_001891
KBio2_004459
KBio2_007027
KBio3_002393
NINDS_000627
CCG-39563
IDI1_000627
NCGC00095864-01
NCGC00095864-02
NS00043275