3-(2-Chloro-phenyl)-propionaldehyde, with the CAS number 157433-36-8, is an organic compound characterized by its aldehyde functional group and a chlorinated aromatic ring. This compound features a propionaldehyde structure, which consists of a three-carbon chain terminating in an aldehyde group, with a 2-chlorophenyl substituent on the second carbon. The presence of the chlorine atom introduces unique reactivity and polarity, influencing its chemical behavior and potential applications. Typically, compounds like this may exhibit properties such as moderate volatility and solubility in organic solvents, while being less soluble in water due to the hydrophobic nature of the aromatic ring. The chlorinated phenyl group can also enhance the compound's biological activity, making it of interest in pharmaceutical and agrochemical research. Additionally, its synthesis and reactivity can be explored in various organic reactions, including nucleophilic additions and substitutions, which are common in the chemistry of aldehydes. Overall, 3-(2-chloro-phenyl)-propionaldehyde is a compound of interest for its structural features and potential applications in synthetic chemistry.

3-(2-CHLORO-PHENYL)-PROPIONALDEHYDE

157433-36-8: 3-(2-Chloro-phenyl)-propionaldehyde, with the CAS number 157433-36-8, is an organic compound characterized by its aldehyde functional group and a chlorinated aromatic ring. This compound features a propionaldehyde structure, which consists of a three-carbon chain terminating in an aldehyde group, with a 2-chlorophenyl substituent on the second carbon. The presence of the chlorine atom introduces unique reactivity and polarity, influencing its chemical behavior and potential applications. Typically, compounds like this may exhibit properties such as moderate volatility and solubility in organic solvents, while being less soluble in water due to the hydrophobic nature of the aromatic ring. The chlorinated phenyl group can also enhance the compound's biological activity, making it of interest in pharmaceutical and agrochemical research. Additionally, its synthesis and reactivity can be explored in various organic reactions, including nucleophilic additions and substitutions, which are common in the chemistry of aldehydes. Overall, 3-(2-chloro-phenyl)-propionaldehyde is a compound of interest for its structural features and potential applications in synthetic chemistry.

CAS 157433-36-8

3-(2-CHLORO-PHENYL)-PROPIONALDEHYDE

3-(2-Chlorophenyl)propanal

Ref: IN-DA001PGG

3-(2-Chlorophenyl)propanal

Ref: 10-F234378