4-Bromochalcone
- Molecular formula
- C9H6BrClO
- CAS Number
- 2524-69-4
- IUPAC Name
- 1-(4-bromophenyl)-3-chloro-prop-2-en-1-one
- Molecular Weight
- 241.51g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4860g/cm3
- Synonyms
- C9H6BrClO
Identification
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.