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

Identification

Molecular formula

C₉H₆Cl₂O

CAS number

77613-97-5

IUPAC name

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

State

At room temperature, 3-chloro-1-(4-chlorophenyl)prop-2-en-1-one is a solid. It is typically stable under standard conditions and should be handled with care due to its possible reactivity with other chemicals.

Melting point (Celsius)

112.00

Melting point (Kelvin)

385.15

Boiling point (Celsius)

307.00

Boiling point (Kelvin)

580.15

General information

Molecular weight

202.06g/mol

Molar mass

202.0580g/mol

Density

1.3400g/cm³

Appearence

3-chloro-1-(4-chlorophenyl)prop-2-en-1-one typically appears as a crystalline solid. It is a chlorinated compound with a light yellow color, often used in organic synthesis for its reactivity and utility in forming larger complex molecules.

Comment on solubility

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

The solubility of 3-chloro-1-(4-chlorophenyl)prop-2-en-1-one, a compound with the chemical formula C₁₀H₈Cl₂O, can be influenced by several factors. Understanding its solubility characteristics is essential for applications in various chemical processes.

Polarity: The presence of halogen atoms, specifically chlorine, contributes to the compound's polar characteristics. This often leads to moderate solubility in polar solvents.
Solvent Compatibility:
- More soluble in organic solvents like acetone and ethanol.
- Limited solubility in water due to its hydrophobic aromatic ring.
Temperature Dependence: Like many organic compounds, solubility may increase with temperature, allowing for better dissolution in solvents.

In conclusion, while 3-chloro-1-(4-chlorophenyl)prop-2-en-1-one exhibits some degree of solubility in organic solvents, it remains largely insoluble in water. This characteristic can be pivotal in its usage and interaction with other compounds in chemical reactions.

Interesting facts

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

3-Chloro-1-(4-chlorophenyl)prop-2-en-1-one is a fascinating compound that belongs to the class of chalcones. This category of compounds has received widespread interest due to their diverse biological activities. Here are some noteworthy features of this specific compound:

Antimicrobial Properties: Numerous studies have demonstrated that chalcone derivatives possess significant antimicrobial activity. 3-Chloro-1-(4-chlorophenyl)prop-2-en-1-one is no exception, showcasing potential effectiveness against various bacteria and fungi.
Cancer Research: Chalcones are often researched for their role in cancer prevention and treatment. This compound has been examined for its ability to induce apoptotic cell death in cancer cells, making it a candidate for further exploration in oncological studies.
Synthesis Versatility: 3-Chloro-1-(4-chlorophenyl)prop-2-en-1-one can be synthesized through various methods, including Claisen-Schmidt condensation. This versatility allows chemists to modify its structure to enhance or alter its properties accordingly.
Natural Occurrence: Chalcone structures are present in numerous natural products, including flavonoids and other plant metabolites. This compound might contribute to the health benefits associated with those plants.
Pharmaceutical Potential: The unique structure of 3-chloro-1-(4-chlorophenyl)prop-2-en-1-one positions it as a promising building block for the development of new pharmaceuticals. The functional groups present can facilitate interactions with biological targets.

In summary, the remarkable properties of 3-chloro-1-(4-chlorophenyl)prop-2-en-1-one highlight its importance in both research and application. Its promising biological activities and potential for synthetic versatility make it a compound of great interest among chemists and biochemists alike.

Synonyms

3,4'-dichloroacrylophenone