Trans-4-(4-Fluorostyryl)phenyl methyl ether

Identification

Molecular formula

C₂₂H₁₇FO

CAS number

139718-82-0

IUPAC name

1-fluoro-4-[2-(4-methoxyphenyl)-2-phenyl-vinyl]benzene

State

At room temperature, Trans-4-(4-Fluorostyryl)phenyl methyl ether exists in a solid state.

Melting point (Celsius)

128.00

Melting point (Kelvin)

401.15

Boiling point (Celsius)

434.00

Boiling point (Kelvin)

707.15

General information

Molecular weight

290.37g/mol

Molar mass

290.3500g/mol

Density

1.1147g/cm³

Appearence

Trans-4-(4-Fluorostyryl)phenyl methyl ether is typically a colorless to light yellow solid. It is crystalline in nature, often appearing as fine, well-defined crystals.

Comment on solubility

Solubility of 1-fluoro-4-[2-(4-methoxyphenyl)-2-phenyl-vinyl]benzene

The solubility of 1-fluoro-4-[2-(4-methoxyphenyl)-2-phenyl-vinyl]benzene can be influenced by several factors, making it a compound of interest in various fields of chemistry.

Factors Affecting Solubility

Polarity: The presence of the fluoro group can increase polarity, affecting how this compound interacts with solvents.
Hydrophobic Interactions: The extensive aromatic rings contribute to hydrophobic interactions, likely reducing solubility in polar solvents.
Temperature: Increased temperature generally enhances solubility for most organic compounds, including this one.

Common Behavior: This compound is likely to be more soluble in organic solvents such as ethanol or chloroform, while being poorly soluble in water due to its hydrophobic characteristics.

In summary, understanding the solubility of 1-fluoro-4-[2-(4-methoxyphenyl)-2-phenyl-vinyl]benzene requires consideration of its molecular structure and the surrounding environment. Effective solubility studies can lead to insights into its applications in various chemical processes.

Interesting facts

Interesting Facts about 1-fluoro-4-[2-(4-methoxyphenyl)-2-phenyl-vinyl]benzene

1-fluoro-4-[2-(4-methoxyphenyl)-2-phenyl-vinyl]benzene is a fascinating compound that belongs to a class of organic chemicals known as aryl vinyl compounds. This compound has garnered interest in both academic and industrial sectors due to its unique structural properties and potential applications.

Key Features

Fluorine Substitution: The presence of a fluorine atom in the structure enhances the compound's reactivity and can modify its electronic and steric properties, making fluorinated compounds particularly interesting in medicinal chemistry.
Vinyl Group: The vinyl group contributes to the compound's ability to undergo addition reactions, which can be leveraged in synthetic organic chemistry to create more complex molecular architectures.
Versatile Applications: Due to its structural characteristics, this compound can be explored for usage in materials science, particularly in the development of light-emitting devices and organic photovoltaics.

Potential Research Implications

Researchers are particularly excited about the implications of compounds like 1-fluoro-4-[2-(4-methoxyphenyl)-2-phenyl-vinyl]benzene in the fields of:

Drug Development: Its unique properties may offer innovative pathways for synthesizing new pharmaceuticals.
Organic Electronics: The compound can be investigated for its role in improving the efficiency of organic electronic components.
Polymer Chemistry: As a building block, it could be used to develop polymers with enhanced mechanical and thermal properties.

In summary, 1-fluoro-4-[2-(4-methoxyphenyl)-2-phenyl-vinyl]benzene serves as a prime example of how organic compounds can possess multifaceted properties that allow them to play significant roles in various scientific advancements. Its intriguing structure provides ample opportunities for discovery and innovation within the chemical sciences.