2-Oxo-2-(4-phenoxyphenyl)acetaldehyde

Molecular formula: C₁₄H₁₀O₃
CAS Number: 93803-56-8
IUPAC Name: 2-oxo-2-(4-phenoxyphenyl)acetaldehyde
Molecular Weight: 240.23g/mol
Melting Point: (Celsius)
Boiling Point: (Celsius)
Density: 1.2760g/cm3
Synonyms: GLYOXAL, (p-PHENOXYPHENYL)-

Interesting facts

Interesting Facts about 2-Oxo-2-(4-phenoxyphenyl)acetaldehyde

2-Oxo-2-(4-phenoxyphenyl)acetaldehyde is an intriguing compound that boasts a number of fascinating attributes, making it interesting from both a scientific and practical viewpoint.

Chemical Structure and Reactivity

This compound is characterized by a ketone functional group alongside an aldehyde, which contributes to its reactivity in various organic reactions. The presence of the 4-phenoxyphenyl moiety enhances its stability and solubility in non-polar solvents, allowing it to engage in substitution reactions that can lead to diverse organic derivatives.

Applications and Uses

Some notable applications of 2-oxo-2-(4-phenoxyphenyl)acetaldehyde include:

Intermediate in Synthesis: This compound serves as an important intermediate for synthesizing optical brighteners, pharmaceuticals, and agrochemicals.
Potential Antimicrobial Activity: Some studies suggest the compound may exhibit antimicrobial properties, making it a candidate for developing new antibacterial agents.
Insights into Aromatic Compounds: As part of a larger family of aromatic ketones and aldehydes, it can provide insight into reactivity and the behavior of numerous other compounds within this class.

Interesting Reactions

This compound is capable of undergo:

Aldol Condensation: Which can lead to the formation of larger, more complex molecules.
Nucleophilic Addition Reactions: Due to its reactive carbonyl groups, it can participate in various nucleophilic attack scenarios.

Research Implications

The study of 2-oxo-2-(4-phenoxyphenyl)acetaldehyde can yield insights not only into organic synthesis but also into materials science, due to its potential use in developing new polymers and coatings that require specific optical properties.