3-Chloro-1-phenyl-2-propen-1-one
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- Molecular formula
- C9H7ClO
- CAS Number
- 20469-36-1
- IUPAC Name
- 3-chloro-1-phenyl-prop-2-en-1-one
- Molecular Weight
- 168.59g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2150g/cm3
- Synonyms
- 3-Chloroacrylophenone
Identification
Interesting facts
Interesting Facts about 3-Chloro-1-phenyl-prop-2-en-1-one
3-Chloro-1-phenyl-prop-2-en-1-one, also known as Chalcone, is a fascinating organic compound with numerous applications and properties that make it a subject of interest for chemists and researchers alike. Here are some captivating points about this compound:
- Versatile Precursor: Chalcones serve as important intermediates in organic synthesis, especially in the creation of flavonoids and other natural products.
- Biological Activities: Studies suggest that compounds with a chalcone structure possess various biological activities, such as anti-inflammatory, antioxidant, and antibacterial properties.
- Photochemical Properties: The unsaturated double bonds in chalcones allow them to exhibit interesting photochemical behavior, making them significant in research related to light-activated reactions.
- Color Producer: Chalcones can act as dyes, contributing to vibrant coloration in various applications, including textiles and biological systems.
- Cross-Coupling Reactions: The presence of the chloro group makes this compound a suitable participant in cross-coupling reactions, which are key for synthesizing more complex organic molecules.
- Research Tool: Due to their diverse range of reactions and bioactivities, chalcones are frequently explored in medicinal chemistry and pharmacology, showcasing their relevance in drug design.
Given the notable properties and applications of 3-chloro-1-phenyl-prop-2-en-1-one, it remains a captivating topic in organic chemistry, fueling ongoing research and development in various scientific fields.