The chemical substance known as (2E)-3-(2-chlorophenyl)-1-(4-hydroxyphenyl)prop-2-en-1-one, with the CAS number 5424-02-2, is an organic compound characterized by its conjugated double bond system, which contributes to its potential as a chromophore. This compound features a prop-2-en-1-one backbone, indicating the presence of a ketone functional group and an alkene, which can exhibit reactivity typical of both functionalities. The presence of a 2-chlorophenyl group and a 4-hydroxyphenyl group suggests that it may possess interesting electronic properties and potential biological activity, possibly acting as a ligand or a precursor in various chemical reactions. The hydroxyl group can also enhance solubility in polar solvents and may participate in hydrogen bonding. Additionally, the compound's structural features may allow it to engage in various intermolecular interactions, making it of interest in fields such as medicinal chemistry and materials science. Overall, this compound's unique structure and functional groups contribute to its potential applications in diverse chemical contexts.

(2E)-3-(2-chlorophenyl)-1-(4-hydroxyphenyl)prop-2-en-1-one

5424-02-2: The chemical substance known as (2E)-3-(2-chlorophenyl)-1-(4-hydroxyphenyl)prop-2-en-1-one, with the CAS number 5424-02-2, is an organic compound characterized by its conjugated double bond system, which contributes to its potential as a chromophore. This compound features a prop-2-en-1-one backbone, indicating the presence of a ketone functional group and an alkene, which can exhibit reactivity typical of both functionalities. The presence of a 2-chlorophenyl group and a 4-hydroxyphenyl group suggests that it may possess interesting electronic properties and potential biological activity, possibly acting as a ligand or a precursor in various chemical reactions. The hydroxyl group can also enhance solubility in polar solvents and may participate in hydrogen bonding. Additionally, the compound's structural features may allow it to engage in various intermolecular interactions, making it of interest in fields such as medicinal chemistry and materials science. Overall, this compound's unique structure and functional groups contribute to its potential applications in diverse chemical contexts.

CAS 5424-02-2

(2E)-3-(2-chlorophenyl)-1-(4-hydroxyphenyl)prop-2-en-1-one

2-Chloro-4'-hydroxychalcone

Ref: 54-OR14419