Ethyl 5-(3,5-dichlorophenyl)-5-oxo-pentanoate, with the CAS number 898751-87-6, is an organic compound characterized by its ester functional group and a distinctive diketone structure. This compound features a pentanoate backbone, which is a five-carbon chain, and is substituted with a 3,5-dichlorophenyl group, contributing to its unique chemical properties. The presence of the dichlorophenyl moiety enhances its potential for biological activity, making it of interest in pharmaceutical research. Ethyl 5-(3,5-dichlorophenyl)-5-oxo-pentanoate is typically a solid or liquid at room temperature, depending on its specific formulation and purity. It is important to handle this compound with care, as it may exhibit toxicity or environmental hazards. Its synthesis often involves standard organic reactions such as esterification and acylation. The compound's reactivity can be influenced by the electron-withdrawing effects of the chlorine atoms, which can affect its interactions in various chemical environments. Overall, this compound represents a class of chemicals that may have applications in medicinal chemistry and agrochemicals.

ethyl 5-(3,5-dichlorophenyl)-5-oxo-pentanoate

898751-87-6: Ethyl 5-(3,5-dichlorophenyl)-5-oxo-pentanoate, with the CAS number 898751-87-6, is an organic compound characterized by its ester functional group and a distinctive diketone structure. This compound features a pentanoate backbone, which is a five-carbon chain, and is substituted with a 3,5-dichlorophenyl group, contributing to its unique chemical properties. The presence of the dichlorophenyl moiety enhances its potential for biological activity, making it of interest in pharmaceutical research. Ethyl 5-(3,5-dichlorophenyl)-5-oxo-pentanoate is typically a solid or liquid at room temperature, depending on its specific formulation and purity. It is important to handle this compound with care, as it may exhibit toxicity or environmental hazards. Its synthesis often involves standard organic reactions such as esterification and acylation. The compound's reactivity can be influenced by the electron-withdrawing effects of the chlorine atoms, which can affect its interactions in various chemical environments. Overall, this compound represents a class of chemicals that may have applications in medicinal chemistry and agrochemicals.

CAS 898751-87-6

ethyl 5-(3,5-dichlorophenyl)-5-oxo-pentanoate

ethyl 5-(3,5-dichlorophenyl)-5-oxovalerate

Ref: 10-F207722