Ethyl 2-cyano-3,3-dicyclopropylacrylate

Identification

Molecular formula

C₁₀H₁₃NO₂

CAS number

109-58-0

IUPAC name

ethyl 2-cyano-3,3-dicyclopropyl-prop-2-enoate

State

At room temperature, ethyl 2-cyano-3,3-dicyclopropylacrylate exists in a liquid state.

Melting point (Celsius)

-60.00

Melting point (Kelvin)

213.15

Boiling point (Celsius)

78.00

Boiling point (Kelvin)

351.15

General information

Molecular weight

219.27g/mol

Molar mass

219.2720g/mol

Density

1.1270g/cm³

Appearence

Ethyl 2-cyano-3,3-dicyclopropylacrylate is typically a clear, colorless liquid. It may have a sharp or sweet odor characteristic of acrylate compounds.

Comment on solubility

Solubility of Ethyl 2-cyano-3,3-dicyclopropyl-prop-2-enoate

Ethyl 2-cyano-3,3-dicyclopropyl-prop-2-enoate, with the chemical formula C₁₃H₁₅N₁O₂, presents intriguing solubility characteristics worth noting:

Polar vs. Nonpolar Solvents: This compound is likely to exhibit greater solubility in polar organic solvents due to the presence of the cyano group, which can interact favorably with polar solvent molecules.
Hydrophobic Character: The dicyclopropyl groups contribute to a degree of hydrophobicity, suggesting limited solubility in aqueous solutions.
Temperature Influence: Like many organic compounds, solubility may increase with temperature, making warmer solvent environments more conducive to dissolving the compound.
Interactions with Solvents: The ability to engage in hydrogen bonding and dipole-dipole interactions can enhance solubility in certain solvents but may also diminish it in others, depending on solvent polarity.

In summary, while ethyl 2-cyano-3,3-dicyclopropyl-prop-2-enoate may show significant solubility in polar organic solvents, its hydrophobic regions might restrict its dissolution in water. Understanding these solubility dynamics is crucial for applications in both laboratory and industrial settings.

Interesting facts

Interesting Facts About Ethyl 2-cyano-3,3-dicyclopropyl-prop-2-enoate

Ethyl 2-cyano-3,3-dicyclopropyl-prop-2-enoate is a fascinating compound that falls into the category of cyano-substituted esters. Here are some intriguing points about this unique substance:

Structural Complexity: The compound features a complex structure that includes a cyano group, a double bond, and multiple cyclopropyl rings. This complexity contributes to its unique chemical reactivity and potential applications.
Pivotal in Synthesis: Ethyl 2-cyano-3,3-dicyclopropyl-prop-2-enoate serves as an important building block in organic synthesis, particularly in the development of other functionalized compounds.
Reactivity: The presence of the cyano group enhances the electrophilic character of the compound, making it a promising candidate for various chemical reactions, including nucleophilic additions and cycloadditions.
Biological Potential: Similar compounds have been studied for their potential biological activities, providing a basis for the exploration of this compound in medicinal chemistry and drug discovery.

In the words of a chemist: “The intricate design of ethyl 2-cyano-3,3-dicyclopropyl-prop-2-enoate opens up a realm of possibilities in synthetic pathways, showcasing nature’s ingenuity at the molecular level.”

As research continues, understanding and harnessing the properties of ethyl 2-cyano-3,3-dicyclopropyl-prop-2-enoate could lead to advancements in diverse fields such as pharmaceuticals, materials science, and beyond.