Malonic acid, di(2-propen-1-yl) ester

Identification

Molecular formula

C₉H₁₂O₄

CAS number

107-29-9

IUPAC name

1-but-2-enoyloxybut-2-enyl but-2-enoate

State

At room temperature, this compound is a liquid.

Melting point (Celsius)

-75.00

Melting point (Kelvin)

198.15

Boiling point (Celsius)

129.00

Boiling point (Kelvin)

402.15

General information

Molecular weight

168.18g/mol

Molar mass

168.1820g/mol

Density

0.9750g/cm³

Appearence

This compound appears as a clear, colorless liquid.

Comment on solubility

Solubility of 1-but-2-enoyloxybut-2-enyl but-2-enoate

The solubility of 1-but-2-enoyloxybut-2-enyl but-2-enoate can be influenced by several factors, as is the case with many chemical compounds. When evaluating solubility, consider the following key points:

Polarity: The **polarity** of the molecule plays a crucial role in its solubility in various solvents. Generally, polar compounds tend to dissolve well in polar solvents (like water), while nonpolar compounds are more soluble in nonpolar solvents (like hexane).
Functional Groups: The presence of functional groups such as esters or alcohols can enhance or reduce solubility. In this compound, the ester groups may contribute to moderate solubility in organic solvents.
Temperature: Solubility can also be dependent on temperature; many compounds become more soluble in warmer conditions.
pH Levels: The pH of the solvent can impact the ionization of the functional groups, thus affecting solubility.

As a summary, while 1-but-2-enoyloxybut-2-enyl but-2-enoate has some solubility in organic solvents due to its ester linkages, its exact solubility characteristics would need to be determined through experimental methods, accounting for the aforementioned factors.

Interesting facts

Interesting Facts about 1-but-2-enoyloxybut-2-enyl but-2-enoate

1-but-2-enoyloxybut-2-enyl but-2-enoate is a fascinating compound, particularly within the realm of synthetic chemistry and materials science. Here are some noteworthy insights about this compound:

Functional Group Diversity: This compound exhibits a rich tapestry of functional groups, featuring both ester and alkene linkages. This structural variety makes it an intriguing candidate for studies in polymer chemistry and organic synthesis.
Synthetic Applications: Its unique structure allows for potential applications in the creation of advanced materials, including coatings and adhesives, which can benefit from enhanced performance characteristics due to its ester functionality.
Reactivity: Due to the presence of multiple double bonds, this compound can undergo various reactions, including polymerization and cross-linking, making it valuable in the development of novel polymers with tailored properties.
Biological Significance: Compounds with similar structures to 1-but-2-enoyloxybut-2-enyl but-2-enoate are of interest in fields such as medicinal chemistry. Understanding its reactivity and potential interactions can contribute to drug design processes.
Green Chemistry: The study of such compounds aligns well with the principles of green chemistry, as their synthesis can potentially be optimized to minimize waste and use renewable resources.

Overall, 1-but-2-enoyloxybut-2-enyl but-2-enoate serves as a prime example of how simple structural modifications can lead to significant variations in chemical behavior and application potential. As researchers continue to explore its properties, it may reveal new pathways to innovative solutions in chemistry.