Chalcone derivative
- Molecular formula
- C15H9ClF2O
- CAS Number
- 51414-25-8
- IUPAC Name
- 3-(2-chloro-4-fluoro-phenyl)-1-(4-fluorophenyl)prop-2-en-1-one
- Molecular Weight
- 290.68g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2836g/cm3
Identification
Exploring 3-(2-chloro-4-fluoro-phenyl)-1-(4-fluorophenyl)prop-2-en-1-one
This intriguing compound belongs to the class of chalcones, a group of compounds known for their unique structural properties and applications in various fields, including medicinal chemistry and materials science. Here are some fascinating aspects of this compound:
- Structural Complexity: The compound showcases a complex arrangement of substituents, featuring both chloro and fluoro groups that significantly influence its chemical behavior.
- Biological Activity: Chalcones, in general, have been studied for their potential pharmacological benefits. This specific compound may exhibit antioxidant, anti-inflammatory, and anticancer properties, making it a candidate for further research.
- Versatile Building Blocks: In organic synthesis, chalcones serve as valuable intermediates for producing diverse compounds, including flavonoids and natural products. The unique reactivity of the double bond in its structure allows for a wide range of modifications.
- Development of Green Chemistry: The synthesis of compounds like this one is often explored in the context of green chemistry to develop sustainable methods that minimize environmental impact.
As a chemistry student or a scientist, understanding the nuances of such compounds is crucial. Their multifaceted roles in both research and practical applications underline the importance of chalcones in modern chemistry. The exploration of compounds like 3-(2-chloro-4-fluoro-phenyl)-1-(4-fluorophenyl)prop-2-en-1-one opens avenues for innovative therapeutic agents and increases our grasp of their role in biological systems. In the words of a prominent chemist, “Every compound tells a story; it's our job to uncover it.”