Ethyl 3-(2,4-dichlorophenyl)-3-oxopropanoate, identified by its CAS number 60868-41-9, is an organic compound characterized by its ester functional group and a ketone moiety. This compound features a 2,4-dichlorophenyl group, which contributes to its potential biological activity and chemical reactivity. Typically, such compounds exhibit moderate to high lipophilicity due to the presence of aromatic rings, which can influence their solubility in organic solvents. Ethyl 3-(2,4-dichlorophenyl)-3-oxopropanoate may be synthesized through various organic reactions, often involving acylation or esterification processes. The presence of chlorine substituents on the phenyl ring can enhance the compound's reactivity and may impart specific pharmacological properties. In terms of safety, like many organic compounds, it should be handled with care, as it may pose risks such as irritation or toxicity. Its applications could range from use in pharmaceuticals to agrochemicals, depending on its biological activity and chemical stability.

ethyl 3-(2,4-dichlorophenyl)-3-oxopropanoate

60868-41-9: Ethyl 3-(2,4-dichlorophenyl)-3-oxopropanoate, identified by its CAS number 60868-41-9, is an organic compound characterized by its ester functional group and a ketone moiety. This compound features a 2,4-dichlorophenyl group, which contributes to its potential biological activity and chemical reactivity. Typically, such compounds exhibit moderate to high lipophilicity due to the presence of aromatic rings, which can influence their solubility in organic solvents. Ethyl 3-(2,4-dichlorophenyl)-3-oxopropanoate may be synthesized through various organic reactions, often involving acylation or esterification processes. The presence of chlorine substituents on the phenyl ring can enhance the compound's reactivity and may impart specific pharmacological properties. In terms of safety, like many organic compounds, it should be handled with care, as it may pose risks such as irritation or toxicity. Its applications could range from use in pharmaceuticals to agrochemicals, depending on its biological activity and chemical stability.

Benzenepropanoic acid, 2,4-dichloro-b-oxo-, ethyl ester

3-(2,4-Dichloro-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester

CAS 60868-41-9

ethyl 3-(2,4-dichlorophenyl)-3-oxopropanoate

Benzenepropanoic acid, 2,4-dichloro-b-oxo-, ethyl ester

Ref: IN-DA00IARM

3-(2,4-Dichloro-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester

Ref: 54-OR1010630

3-(2,4-Dichlorophenyl)-3-oxo-propionic acid ethyl ester

Ref: 10-F014870