Skip to main content

3-(4-Chlorophenyl)-3-chloroprop-2-enal

ADVERTISEMENT
Identification
Molecular formula
C9H6Cl2O
CAS number
3535-25-7
IUPAC name
3-chloro-3-(4-chlorophenyl)prop-2-enal
State
State

At room temperature, the compound is in a solid state. It has a noticeable crystalline form with a pale yellow hue.

Melting point (Celsius)
87.00
Melting point (Kelvin)
360.15
Boiling point (Celsius)
317.00
Boiling point (Kelvin)
590.15
General information
Molecular weight
186.06g/mol
Molar mass
186.0590g/mol
Density
1.2640g/cm3
Appearence

3-(4-Chlorophenyl)-3-chloroprop-2-enal is a light yellow to beige solid. It is typically used in laboratory research and has a crystalline appearance.

Comment on solubility

Solubility Characteristics of 3-Chloro-3-(4-chlorophenyl)prop-2-enal

3-chloro-3-(4-chlorophenyl)prop-2-enal, a compound with a complex structure, exhibits moderate solubility properties in various solvents. Understanding its solubility can be nuanced due to several factors:

  • Polarity: The presence of chlorine atoms contributes to the compound's polar character, influencing its interaction with polar solvents.
  • Solvent Type: This compound tends to be more soluble in organic solvents such as ethanol and acetone, while showing limited solubility in water due to its hydrophobic aromatic rings.
  • Temperature Variations: Increased temperature generally enhances solubility, making the compound more soluble in higher temperatures but not drastically changing its overall solubility profile.

In practical applications, it’s often recommended to conduct solubility assessments under varying conditions to determine the best solvent for desired outcomes. As noted in the literature, "solubility can greatly affect the compound's behavior in chemical reactions, biological processes, and industrial applications." Hence, understanding these solubility factors is critical for effective utilization of 3-chloro-3-(4-chlorophenyl)prop-2-enal in various fields.

Interesting facts

Interesting Facts about 3-chloro-3-(4-chlorophenyl)prop-2-enal

3-chloro-3-(4-chlorophenyl)prop-2-enal is a fascinating compound that plays a significant role in both organic chemistry and medicinal chemistry. Its unique structure and functional groups contribute to its diverse applications. Here are some intriguing aspects of this compound:

  • Reactivity: This compound is known for its susceptibility to nucleophilic attacks due to the presence of the carbonyl group (aldehyde). This makes it a valuable intermediate in the synthesis of more complex molecules.
  • Biological Activity: Compounds similar to 3-chloro-3-(4-chlorophenyl)prop-2-enal are often explored for their potential antimicrobial and anti-inflammatory properties, indicating its relevance in drug discovery.
  • Structural Importance: The chlorinated benzene ring enhances the compound's stability and reactivity. This structural feature can help in modulating biological activity, making it an interesting candidate for pharmaceutical development.
  • Cross-Linking Agent: Due to its reactive nature, this compound can serve as a cross-linking agent in various chemical processes, particularly in the synthesis of polymers.

In summary, 3-chloro-3-(4-chlorophenyl)prop-2-enal not only highlights the complexities of organic synthesis but also serves as a bridge to understanding various biochemical pathways. As stated by a prominent chemist, "Every compound tells a story; it is our task to interpret its narrative." This compound's story continues to unfold as researchers delve into its potential applications!

Synonyms
DTXSID401285136
3-Chloro-3-(4-chlorophenyl)-2-propenal
DTXCID101715823
SCHEMBL2559262
IWQMAUVMLFGNGU-UHFFFAOYSA-N
3-(4-chlorophenyl)-3-chloroacrolein