Interesting facts
Interesting Facts about 1-(4-bromophenyl)-3-chloro-prop-2-en-1-one
This compound, known as a derivative of chalcone, is part of a fascinating class of organic compounds that exhibit a range of biological activities. Researchers often find themselves intrigued by the properties and potential applications of 1-(4-bromophenyl)-3-chloro-prop-2-en-1-one.
Key Highlights:
- Biological Significance: Chalcone derivatives, including this compound, have been studied for their potential in medicinal chemistry. They may exhibit anti-inflammatory, antimicrobial, and anticancer properties.
- Structure-Activity Relationship: The presence of bromine and chlorine substituents significantly influences the compound's reactivity and biological profile, making it a target of interest for drug design.
- Synthetic Versatility: The synthetic routes to produce this compound often involve methods such as Claisen-Schmidt condensation, allowing chemists to explore various modifications to enhance its functionality.
- Fluorescent Properties: Some chalcone derivatives are known to exhibit fluorescence, which opens up possibilities for their use in imaging applications and sensors.
As chemists delve into the world of 1-(4-bromophenyl)-3-chloro-prop-2-en-1-one, it becomes increasingly clear that this compound is not just a simple molecule but a gateway to understanding complex interactions within biological systems. “Each molecule tells a story,” they say, and this compound is no exception. Its unique structure invites further exploration and paves the way for future innovations in pharmaceuticals.
Synonyms
C9H6BrClO
CBiol_000675
SCHEMBL4738896
DTXSID201270460
ICCB3_000323
1-(4-Bromophenyl)-3-chloro-2-propen-1-one
Solubility of 1-(4-bromophenyl)-3-chloro-prop-2-en-1-one
When exploring the solubility of 1-(4-bromophenyl)-3-chloro-prop-2-en-1-one, it is important to consider several factors that influence how this compound behaves in various solvents.
This compound is likely to exhibit limited solubility in water due to its significant hydrophobic (water-repelling) characteristics stemming from the presence of the aromatic 4-bromophenyl group. Conversely, it may show increased solubility in organic solvents. Here are some insights:
In summary, while the solubility of 1-(4-bromophenyl)-3-chloro-prop-2-en-1-one in water is expected to be low, its presence in non-polar solvents will likely prove more favorable, highlighting the importance of solvent selection in applications involving this compound.