Skip to main content

3-chloro-1-(4-iodophenyl)prop-2-en-1-one

ADVERTISEMENT
Identification
Molecular formula
C9H6ClIO
CAS number
2112-26-1
IUPAC name
3-chloro-1-(4-iodophenyl)prop-2-en-1-one
State
State

At room temperature, 3-chloro-1-(4-iodophenyl)prop-2-en-1-one is generally found in a solid state. Its stability and appearance can be affected by environmental factors such as humidity and temperature.

Melting point (Celsius)
110.00
Melting point (Kelvin)
383.15
Boiling point (Celsius)
247.00
Boiling point (Kelvin)
520.15
General information
Molecular weight
310.50g/mol
Molar mass
310.4990g/mol
Density
1.6730g/cm3
Appearence

3-Chloro-1-(4-iodophenyl)prop-2-en-1-one typically presents as a solid with a pale yellow color. The compound may crystallize in certain forms depending on its purification process, and its crystalline structure can be either fine or coarse.

Comment on solubility

Solubility of 3-chloro-1-(4-iodophenyl)prop-2-en-1-one

The solubility of 3-chloro-1-(4-iodophenyl)prop-2-en-1-one in various solvents can be influenced by its specific chemical structure and the presence of both chlorine and iodine substituents on its aromatic ring. Here are some key points regarding its solubility:

  • Polar solvents: This compound is expected to have limited solubility in polar solvents such as water due to the non-polar character of the aromatic groups.
  • Non-polar solvents: It is likely to be more soluble in non-polar organic solvents, such as dichloromethane or hexane, which can better solvate the hydrophobic parts of the molecule.
  • Concentration-dependent: The solubility may vary based on concentration and temperature, with increased solubility being likely at elevated temperatures.

In summary, due to its complex structure, 3-chloro-1-(4-iodophenyl)prop-2-en-1-one may demonstrate preferential solubility in organic solvents, while exhibiting challenges in polar environments. Understanding these solubility characteristics is crucial for applications in synthesis and formulation.

Interesting facts

Interesting Facts about 3-Chloro-1-(4-iodophenyl)prop-2-en-1-one

3-Chloro-1-(4-iodophenyl)prop-2-en-1-one is a fascinating chemical compound that belongs to the class of chalcones, which are known for their intriguing structural features and biological activities. Here are some notable points about this compound:

  • Origin and Structure: As a chalcone, it features a central α,β-unsaturated carbonyl unit. This structural aspect is essential for its biological activity and potential pharmaceutical applications.
  • Biological Activity: Compounds in the chalcone family, including 3-chloro-1-(4-iodophenyl)prop-2-en-1-one, have been studied for their antioxidant, anti-inflammatory, and anticancer properties. Research indicates that their conjugated system can influence cell signaling pathways.
  • Substituent Effects: The presence of chlorine and iodine in the molecule can significantly alter its reactivity and biological activity. Halogen substitutions often enhance the lipophilicity and bioavailability of compounds, making them more effective in biological systems.
  • Application in Organic Synthesis: Chalcones like this one serve as important intermediates in organic synthesis. Their unique reactivity allows them to be used in the synthesis of various complex organic molecules, including natural products and pharmaceuticals.
  • Harvesting Interests: The unique combination of halogens in 3-chloro-1-(4-iodophenyl)prop-2-en-1-one makes it a subject of interest for researchers investigating new compounds with enhanced biological properties.

In summary, 3-chloro-1-(4-iodophenyl)prop-2-en-1-one is not only a visually interesting compound but also a promising candidate for further research in medicinal chemistry. As stated by chemists: "Chemical diversity is the foundation of innovation in drug discovery." This compound exemplifies that principle beautifully.