The chemical substance known as (2E)-3-(4-chlorophenyl)-1-(4-fluorophenyl)prop-2-en-1-one, with the CAS number 28081-12-1, is an organic compound characterized by its conjugated double bond system and the presence of halogen substituents on the aromatic rings. This compound features a prop-2-en-1-one backbone, which indicates it has both an alkene and a ketone functional group, contributing to its reactivity and potential applications in organic synthesis. The presence of a 4-chlorophenyl group and a 4-fluorophenyl group enhances its electronic properties, potentially influencing its behavior in chemical reactions and interactions with biological systems. Such compounds often exhibit interesting pharmacological activities, making them of interest in medicinal chemistry. Additionally, the geometric configuration (E) denotes the specific arrangement of substituents around the double bond, which can significantly affect the compound's physical and chemical properties, including its stability, solubility, and reactivity. Overall, this compound exemplifies the complexity and diversity of organic molecules used in various chemical applications.

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

28081-12-1: The chemical substance known as (2E)-3-(4-chlorophenyl)-1-(4-fluorophenyl)prop-2-en-1-one, with the CAS number 28081-12-1, is an organic compound characterized by its conjugated double bond system and the presence of halogen substituents on the aromatic rings. This compound features a prop-2-en-1-one backbone, which indicates it has both an alkene and a ketone functional group, contributing to its reactivity and potential applications in organic synthesis. The presence of a 4-chlorophenyl group and a 4-fluorophenyl group enhances its electronic properties, potentially influencing its behavior in chemical reactions and interactions with biological systems. Such compounds often exhibit interesting pharmacological activities, making them of interest in medicinal chemistry. Additionally, the geometric configuration (E) denotes the specific arrangement of substituents around the double bond, which can significantly affect the compound's physical and chemical properties, including its stability, solubility, and reactivity. Overall, this compound exemplifies the complexity and diversity of organic molecules used in various chemical applications.

CAS 28081-12-1

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

3-(4-Chlorophenyl)-1-(4-fluorophenyl)prop-2-en-1-one

Ref: IN-DA00BDMQ

4-Chloro-4'-fluorochalcone

Ref: 54-PC3946

4-Chloro-4′-fluorochalcone

Ref: 10-F493950