2-Bromo-1-chloro-4-(ethylcarbonyl)benzene is an organic compound characterized by the presence of both bromine and chlorine substituents on a benzene ring, along with an ethylcarbonyl group. This compound features a bromine atom at the second position and a chlorine atom at the first position of the benzene ring, while the ethylcarbonyl group is attached at the para position (fourth position). The presence of these halogen atoms contributes to its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. The ethylcarbonyl group introduces a carbonyl functionality, which can participate in further chemical transformations, such as condensation reactions. The compound's structure suggests it may exhibit moderate to high lipophilicity due to the aromatic system and alkyl substituents, influencing its solubility in organic solvents. Additionally, the presence of halogens may impart unique electronic properties, affecting its behavior in chemical reactions and interactions with biological systems. Overall, this compound's unique functional groups and substituents make it of interest in synthetic organic chemistry and potential applications in pharmaceuticals or agrochemicals.

2-bromo-1-chloro-4-(ethylcarbonyl)benzene

1261527-19-8: 2-Bromo-1-chloro-4-(ethylcarbonyl)benzene is an organic compound characterized by the presence of both bromine and chlorine substituents on a benzene ring, along with an ethylcarbonyl group. This compound features a bromine atom at the second position and a chlorine atom at the first position of the benzene ring, while the ethylcarbonyl group is attached at the para position (fourth position). The presence of these halogen atoms contributes to its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. The ethylcarbonyl group introduces a carbonyl functionality, which can participate in further chemical transformations, such as condensation reactions. The compound's structure suggests it may exhibit moderate to high lipophilicity due to the aromatic system and alkyl substituents, influencing its solubility in organic solvents. Additionally, the presence of halogens may impart unique electronic properties, affecting its behavior in chemical reactions and interactions with biological systems. Overall, this compound's unique functional groups and substituents make it of interest in synthetic organic chemistry and potential applications in pharmaceuticals or agrochemicals.

CAS 1261527-19-8

2-bromo-1-chloro-4-(ethylcarbonyl)benzene

1-Propanone, 1-(3-bromo-4-chlorophenyl)-

Ref: IN-DA000RUH