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Cinnamyl phenethyl ether

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Identification
Molecular formula
C17H18O2
CAS number
122-97-4
IUPAC name
2-phenylethyl 3-phenylprop-2-enoate
State
State

At room temperature, cinnamyl phenethyl ether is a liquid, which can appear clear or very slightly yellow.

Melting point (Celsius)
2.00
Melting point (Kelvin)
275.15
Boiling point (Celsius)
310.00
Boiling point (Kelvin)
583.15
General information
Molecular weight
238.32g/mol
Molar mass
238.3100g/mol
Density
1.0851g/cm3
Appearence

This compound is typically a colorless or pale yellow liquid with a pleasant floral odor. It is often used in the fragrance industry.

Comment on solubility

Solubility of 2-phenylethyl 3-phenylprop-2-enoate

The solubility of 2-phenylethyl 3-phenylprop-2-enoate in different solvents is an interesting aspect to consider, especially because of its unique structure. This compound, characterized by its phenyl-substituted groups, demonstrates variable solubility traits influenced by several factors:

  • Polar vs. Non-polar Solvents: 2-phenylethyl 3-phenylprop-2-enoate is generally more soluble in non-polar and weakly polar solvents. This is due to the presence of the aromatic rings which favor interactions with similar solvation environments.
  • Temperature Effects: Like many organic compounds, its solubility can increase with rising temperatures, as the increased kinetic energy helps disrupt intermolecular forces.
  • Molecular Interactions: This compound may exhibit hydrophobic interactions in water due to its bulky aromatic structure, resulting in low solubility in aqueous environments.

In conclusion, while 2-phenylethyl 3-phenylprop-2-enoate is likely to be soluble in organic solvents such as ethanol or chloroform, it will struggle to dissolve in polar solvents like water, making knowledge of its solubility properties essential for applications across various fields, particularly in organic synthesis and formulation chemistry.

Interesting facts

Interesting Facts About 2-Phenylethyl 3-phenylprop-2-enoate

2-Phenylethyl 3-phenylprop-2-enoate is an intriguing compound that falls within the category of esters, known for their fragrant qualities and diverse applications.

Chemical Features

This compound can be characterized by several notable features, which include:

  • Functional Groups: It showcases the presence of both an ester and an alkene functional group, leading to its unique reactivity and properties.
  • Aromatic Rings: The presence of phenyl groups enhances its stability and introduces interesting electron-donating characteristics.
  • Structural Isomerism: This compound's structure allows for various isomers, adding to its chemical intrigue for organic chemists.

Applications and Uses

2-Phenylethyl 3-phenylprop-2-enoate holds significance in various fields:

  • Fragrance Industry: Its sweet floral aroma makes it a potential candidate for fragrances and perfumes.
  • Flavoring Agent: It can be used as a flavoring agent in food products, contributing to a variety of tastes.
  • Pharmaceuticals: The compound's unique properties may find applications in drug formulation, especially due to its ester nature.

Chemical Reactions

This compound is capable of participating in several types of reactions:

  • Esterification: It can undergo reactions to form new esters, leading to the synthesis of a variety of compounds.
  • Hydrolysis: In the presence of water, it can break down to yield its alcohol and acid components.
  • Addition Reactions: The double bond in its structure allows it to engage in addition reactions, expanding its synthetic applications.

In conclusion, 2-phenylethyl 3-phenylprop-2-enoate is not just a simple chemical compound; it embodies a world of possibilities in terms of synthesis, aroma, and application. As scientists explore its potential further, we may uncover even more exciting uses for this versatile ester.

Synonyms
103-53-7
Cinnamic Acid Phenethyl Ester
Cinnamic Acid 2-Phenylethyl Ester
Phenethyl 3-Phenylacrylate
SCHEMBL43631
CHEMBL3184894
AKOS028108456
SY051978
P2007