N-allyloxy-1-(7-bicyclo[4.2.0]octa-1,3,5-trienyl)ethanimine

Identification

Molecular formula

C₁₄H₁₇NO

CAS number

Not Available

IUPAC name

N-allyloxy-1-(7-bicyclo[4.2.0]octa-1,3,5-trienyl)ethanimine

State

At room temperature, it is generally in a liquid state.

Melting point (Celsius)

-10.00

Melting point (Kelvin)

263.15

Boiling point (Celsius)

265.00

Boiling point (Kelvin)

538.15

General information

Molecular weight

203.28g/mol

Molar mass

203.2820g/mol

Density

1.1200g/cm³

Appearence

N-allyloxy-1-(7-bicyclo[4.2.0]octa-1,3,5-trienyl)ethanimine is typically a colorless to pale yellow liquid. It may exhibit a slightly pungent odor, characteristic of many aliphatic ethers and imines.

Comment on solubility

Solubility of N-allyloxy-1-(7-bicyclo[4.2.0]octa-1,3,5-trienyl)ethanimine

N-allyloxy-1-(7-bicyclo[4.2.0]octa-1,3,5-trienyl)ethanimine presents a unique solubility profile that warrants examination. This complex organic compound features both aliphatic and aromatic characteristics, which can influence its interaction with solvents.

Factors Affecting Solubility

Several key factors contribute to the solubility of this compound:

Functional Groups: The presence of the allyloxy group suggests potential solubility in polar solvents, while the bicyclic structure may complicate this interaction.
Polarity: The overall polarity of N-allyloxy-1-(7-bicyclo[4.2.0]octa-1,3,5-trienyl)ethanimine influences its solubility in various solvents.
Hydrogen Bonding: The potential for hydrogen bonding can enhance solubility in protic solvents.
Temperature: Increased temperatures often facilitate solubility by overcoming lattice energies and enhancing molecular interactions.

General Solubility Insights

In general, compounds like N-allyloxy-1-(7-bicyclo[4.2.0]octa-1,3,5-trienyl)ethanimine may exhibit:

Increased solubility in organic solvents such as ethanol and acetone.
Lesser solubility in water, due to the hydrophobic nature of the bicyclic structure.
Variable solubility under different conditions, prompting experimentation to determine the most suitable solvent blend.

Understanding the solubility of this compound is crucial for its application in various chemical processes, as it dictates how the compound interacts with other substances in solution.

Interesting facts

Interesting Facts about N-allyloxy-1-(7-bicyclo[4.2.0]octa-1,3,5-trienyl)ethanimine

N-allyloxy-1-(7-bicyclo[4.2.0]octa-1,3,5-trienyl)ethanimine is a fascinating compound that combines elements of organic synthesis with unique structural characteristics. Here are some intriguing aspects worth noting:

Structural Complexity: This compound features a bicyclic structure, which is noteworthy for its rigid framework and the potential for intricate stereoisomerism.
Hybrid Properties: With the presence of both allyloxy and imine functional groups, this compound can exhibit unique chemical reactivity, making it a valuable target for organic synthesis.
Research Interest: Scientists are increasingly interested in compounds like N-allyloxy-1-(7-bicyclo[4.2.0]octa-1,3,5-trienyl)ethanimine for their potential applications in materials science, organic electronics, and medicinal chemistry.
Pioneer in Synthesis: The synthesis of this compound is an excellent opportunity for chemists to explore complex multi-step reactions, including cycloaddition and functional group modifications.
Mechanistic Insights: Understanding the reactivity patterns of this compound can provide valuable insights into reaction mechanisms that govern larger classes of organic compounds.

In the words of chemist Marie Curie: "Nothing in life is to be feared; it is only to be understood." This quote resonates strongly with the study of complex compounds such as this one, where understanding their unique properties leads to exciting scientific discoveries.

With ongoing research, N-allyloxy-1-(7-bicyclo[4.2.0]octa-1,3,5-trienyl)ethanimine is poised to uncover new frontiers in chemistry, enhancing our knowledge of molecular interactions and transformations.