The chemical substance known as (2E)-1-(4-chlorophenyl)-3-(2,4-dichlorophenyl)prop-2-en-1-one, with the CAS number 133031-38-6, is an organic compound characterized by its conjugated double bond system and the presence of multiple chlorine substituents on its phenyl rings. This compound features a prop-2-en-1-one backbone, indicating it is an α,β-unsaturated ketone, which contributes to its reactivity, particularly in electrophilic addition reactions. The presence of the 4-chlorophenyl and 2,4-dichlorophenyl groups enhances its lipophilicity and may influence its biological activity. The chlorine atoms can also affect the compound's electronic properties, potentially making it a candidate for various applications in pharmaceuticals or agrochemicals. Additionally, the geometric configuration (E) indicates that the substituents on the double bond are on opposite sides, which can impact the compound's physical properties, such as melting and boiling points, as well as its interaction with biological targets. Overall, this compound's unique structure and substituents suggest it may exhibit interesting chemical behavior and potential utility in various fields.

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

133031-38-6: The chemical substance known as (2E)-1-(4-chlorophenyl)-3-(2,4-dichlorophenyl)prop-2-en-1-one, with the CAS number 133031-38-6, is an organic compound characterized by its conjugated double bond system and the presence of multiple chlorine substituents on its phenyl rings. This compound features a prop-2-en-1-one backbone, indicating it is an α,β-unsaturated ketone, which contributes to its reactivity, particularly in electrophilic addition reactions. The presence of the 4-chlorophenyl and 2,4-dichlorophenyl groups enhances its lipophilicity and may influence its biological activity. The chlorine atoms can also affect the compound's electronic properties, potentially making it a candidate for various applications in pharmaceuticals or agrochemicals. Additionally, the geometric configuration (E) indicates that the substituents on the double bond are on opposite sides, which can impact the compound's physical properties, such as melting and boiling points, as well as its interaction with biological targets. Overall, this compound's unique structure and substituents suggest it may exhibit interesting chemical behavior and potential utility in various fields.

1-(4-chlorophenyl)-3-(2,4-dichlorophenyl)prop-2-en-1-one

CAS 133031-38-6

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

1-(4-chlorophenyl)-3-(2,4-dichlorophenyl)prop-2-en-1-one

Ref: 54-OR24794