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Eugeniin

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Identification
Molecular formula
C17H20O5
CAS number
None available
IUPAC name
2-ethoxyethyl 3-(4-methoxyphenyl)prop-2-enoate
State
State

At room temperature, Eugeniin is found as a solid.

Melting point (Celsius)
65.00
Melting point (Kelvin)
338.15
Boiling point (Celsius)
336.00
Boiling point (Kelvin)
609.15
General information
Molecular weight
308.39g/mol
Molar mass
308.3900g/mol
Density
1.0793g/cm3
Appearence

Eugeniin appears as a white to off-white crystalline powder. It is known for being a stable compound under normal conditions and is usually handled as a solid substance.

Comment on solubility

Solubility of 2-ethoxyethyl 3-(4-methoxyphenyl)prop-2-enoate

The solubility of 2-ethoxyethyl 3-(4-methoxyphenyl)prop-2-enoate in various solvents can be quite interesting due to its unique chemical structure. Typically, solubility is influenced by factors such as polarity, molecular size, and intermolecular interactions.

Key Points on Solubility:

  • Polarity: This compound features an ethoxy group, which tends to be more polar, making it soluble in polar solvents like water to a certain extent.
  • Solvent Compatibility: It is likely to show good solubility in organic solvents such as ethanol, acetone, and chloroform, owing to its relatively large aromatic (methoxyphenyl) group.
  • Temperature Effect: Increased temperature generally enhances solubility; thus, heating the solvent may improve the dissolution process significantly.
  • Concentration Dependency: At higher concentrations, the solubility may change due to saturation, leading to precipitation or phase separation.

In summary, while 2-ethoxyethyl 3-(4-methoxyphenyl)prop-2-enoate exhibits variations in solubility based on the solvent's characteristics, it generally displays a good solubility profile in suitable organic solvents, making it a versatile compound for chemical applications. As the saying goes, “like dissolves like,” and understanding this principle can aid in predicting its behavior in various environments.

Interesting facts

Interesting Facts About 2-Ethoxyethyl 3-(4-Methoxyphenyl)prop-2-enoate

2-Ethoxyethyl 3-(4-methoxyphenyl)prop-2-enoate, also known as a versatile compound in the realm of organic chemistry, presents a rich landscape for exploration. Below are some noteworthy points about this compound:

  • Functional Groups: This compound features multiple functional groups, including an ester and an alkene. These groups contribute to its reactivity and the potential for further modification in synthetic organic chemistry.
  • Applications: 2-Ethoxyethyl 3-(4-methoxyphenyl)prop-2-enoate has potential applications in pharmaceuticals and agrochemicals due to its unique structure, which may allow for interactions that are beneficial in drug design or pesticide formulation.
  • Reactivity: The presence of the prop-2-enoate moiety indicates the possibility of undergoing Michael addition reactions, which can lead to the formation of complex molecular architectures. Such reactivity is crucial in building more intricate organic compounds.
  • Structure-Activity Relationship (SAR): Analyzing this compound's structure can help scientists understand how modifications to the methoxy and ethoxy groups influence biological activity and solubility, paving the way for optimized drug candidates.
  • Research Interest: The compound has drawn interest in materials science for its potential utility in the development of advanced polymeric materials through polymerization reactions.
  • Interdisciplinary Appeal: This compound's complex structure invites collaboration across disciplines, including medicinal chemistry, materials science, and chemical engineering.

Overall, 2-ethoxyethyl 3-(4-methoxyphenyl)prop-2-enoate exemplifies how carefully structured organic compounds can lead to significant advancements in various scientific fields, embodying the spirit of innovation and discovery in chemistry.

Synonyms
Giv Tan F; Give-Tan; Phiasol; Sundare
ethoxyethyl-p-methoxycinnamate
CHEMBL3560776
CMDKPGRTAQVGFQ-UHFFFAOYSA-N
AKOS028110686