4-(3-phenylprop-2-enoyloxy)butyl 2-oxopropanoate

Identification

Molecular formula

C₁₄H₁₆O₅

CAS number

53941-19-2

IUPAC name

4-(3-phenylprop-2-enoyloxy)butyl 2-oxopropanoate

State

At room temperature, this compound is typically found in the liquid state. It is often stored under specific conditions to maintain its stability and prevent degradation.

Melting point (Celsius)

-10.00

Melting point (Kelvin)

263.15

Boiling point (Celsius)

320.00

Boiling point (Kelvin)

593.15

General information

Molecular weight

248.27g/mol

Molar mass

248.2660g/mol

Density

1.0576g/cm³

Appearence

The compound appears as a colorless to light yellow liquid, often transparent in nature depending on the level of purity. It may exhibit a faint aromatic odor.

Comment on solubility

Solubility of 4-(3-phenylprop-2-enoyloxy)butyl 2-oxopropanoate

The solubility of 4-(3-phenylprop-2-enoyloxy)butyl 2-oxopropanoate is an intriguing aspect to consider. Due to its unique structure, which includes both hydrophobic phenyl groups and more polar functional groups, the solubility characteristics can be quite complex.

Factors Influencing Solubility:

Hydrophobic Interactions: The presence of the phenyl group may lead to increased hydrophobicity, potentially reducing solubility in water.
Polar Functional Groups: The presence of the ester linkages and ketone can enhance solubility in polar solvents, such as alcohols or acetone.
Temperature: Solubility often increases with temperature, which could be relevant for applications involving this compound.

It is often observed that compounds similar to 4-(3-phenylprop-2-enoyloxy)butyl 2-oxopropanoate exhibit moderate solubility in organic solvents while being less soluble in water. This phenomenon can be summarized as:

“A balance between hydrophobic and hydrophilic characteristics ultimately dictates solubility.”

In conclusion, while 4-(3-phenylprop-2-enoyloxy)butyl 2-oxopropanoate may face limitations in aqueous environments, its solubility in organic solvents presents versatile opportunities for various applications.

Interesting facts

Interesting Facts about 4-(3-phenylprop-2-enoyloxy)butyl 2-oxopropanoate

The compound 4-(3-phenylprop-2-enoyloxy)butyl 2-oxopropanoate, commonly known for its unique structure, showcases intriguing properties relevant to both organic chemistry and material sciences. Here are some compelling insights:

Versatile Applications: This compound serves as a versatile reactant in the synthesis of various polymers and coatings, demonstrating its importance in materials science.
Medicinal Chemistry: With phenyl groups integrated into its structure, this compound may exhibit biological activity and potential medicinal applications, making it a subject of interest in pharmacological research.
Reactivity: The presence of both an ester and an enoyloxy functional group allows for diverse reactivity patterns, offering chemists a range of pathways for further chemical transformations.
Study of Structure-Activity Relationship (SAR): The unique blend of functional groups makes it an excellent candidate for studying how structural changes can alter biological activity, providing insights valuable for drug design.
Potential in Organic Synthesis: As a building block, this compound can enable the creation of more complex molecules through methods such as esterification and Michael addition.

In summary, 4-(3-phenylprop-2-enoyloxy)butyl 2-oxopropanoate is not only a fascinating compound due to its structural features but also a potential cornerstone in various scientific disciplines, from materials science to medicinal chemistry. Its reactivity and applicability make it a noteworthy subject for continued research and exploration.