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4-Chlorocinnamonitrile

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Identification
Molecular formula
C9H6ClN
CAS number
25343-39-1
IUPAC name
3-(4-chlorophenyl)prop-2-enenitrile
State
State
4-Chlorocinnamonitrile is usually found as a crystalline solid at room temperature.
Melting point (Celsius)
87.00
Melting point (Kelvin)
360.00
Boiling point (Celsius)
274.00
Boiling point (Kelvin)
547.00
General information
Molecular weight
149.59g/mol
Molar mass
149.5880g/mol
Density
1.1320g/cm3
Appearence

4-Chlorocinnamonitrile typically appears as a yellow to amber-colored crystalline solid.

Comment on solubility

Solubility of 3-(4-chlorophenyl)prop-2-enenitrile

3-(4-chlorophenyl)prop-2-enenitrile, also known as a nitrile compound, can exhibit variable solubility characteristics. Its solubility is mainly influenced by factors such as polarity, molecular structure, and interactions with solvents. Here are some key points to consider:

  • Polarity: Nitriles generally possess a polar carbon-nitrogen triple bond, which may interact favorably with polar solvents.
  • Solvent Type: This compound is likely to be more soluble in polar aprotic solvents (e.g., acetone, acetonitrile) due to the ability of these solvents to stabilize the nitrile functional group.
  • Hydrophobic Factors: The presence of a chlorophenyl group can add hydrophobic characteristics, potentially reducing solubility in highly polar solvents like water.
  • Concentration Dependence: The solubility can change with temperature and concentration, which means it could dissolve better at elevated temperatures or in concentrated solutions.

In conclusion, while exact solubility data may not be widely available, it can be inferred that 3-(4-chlorophenyl)prop-2-enenitrile likely demonstrates moderate solubility in specific polar solvents, while exhibiting limited solubility in aqueous environments. Testing in various solvent systems could provide further insights into its solubility behavior.

Interesting facts

Interesting Facts about 3-(4-chlorophenyl)prop-2-enenitrile

3-(4-chlorophenyl)prop-2-enenitrile is a fascinating compound with noteworthy applications and characteristics. Here are some interesting insights into this compound:

  • Structure Insights: This compound features a unique structural arrangement that includes a chlorophenyl group and a nitrile functional group. Its distinctive double bond contributes to its reactivity, enabling various chemical transformations.
  • Synthetic Utility: Due to its reactive nature, 3-(4-chlorophenyl)prop-2-enenitrile serves as an important intermediate in organic synthesis. It can be utilized in the preparation of pharmaceuticals, agrochemicals, and other fine chemicals.
  • Biological Significance: Compounds like 3-(4-chlorophenyl)prop-2-enenitrile are often studied for their potential biological activities. Research has indicated that derivatives of such compounds may exhibit anti-cancer and anti-inflammatory properties. This makes them intriguing candidates for further pharmacological exploration.
  • Environmental Impact: The presence of halogens, such as chlorine, in the compound can affect its environmental behavior. Understanding how such compounds interact with the environment is essential for assessing their safety and sustainability.
  • Reactivity: The vinyl group in this compound makes it susceptible to electrophilic additions and other reaction pathways, expanding its versatility in synthetic chemistry.

This compound exemplifies the intricate relationship between molecular structure and function, making it a valuable substance in both industrial and academic chemistry settings. As the study of such compounds continues to evolve, their role in diverse applications remains a topic of significant interest.

Synonyms
3-(4-chlorophenyl)prop-2-enenitrile
MFCD00001932
(2E)-3-(4-chlorophenyl)prop-2-enenitrile
SCHEMBL596410
PPCNBCKABHGVMX-UHFFFAOYSA-N
DTXSID001292179
3-(4-chloro-phenyl)-acrylonitrile
AKOS016881889
DB-093976