2-Chloro-1-(3,4-dimethylphenyl)ethanone, with the CAS number 50690-08-9, is an organic compound characterized by its ketone functional group and the presence of a chlorine atom. This compound features a chloro substituent on the first carbon of the ethanone moiety and a 3,4-dimethylphenyl group attached to the carbonyl carbon. Its molecular structure contributes to its reactivity, making it useful in various synthetic applications, particularly in organic synthesis and medicinal chemistry. The presence of the chlorine atom can enhance electrophilicity, facilitating nucleophilic attack in reactions. Additionally, the dimethylphenyl group may influence the compound's physical properties, such as solubility and boiling point, due to steric effects and hydrophobic interactions. As with many organic compounds, safety precautions should be taken when handling this substance, as it may pose health risks if ingested or inhaled. Overall, 2-chloro-1-(3,4-dimethylphenyl)ethanone serves as a valuable intermediate in the synthesis of more complex organic molecules.

2-chloro-1-(3,4-dimethylphenyl)ethanone

50690-08-9: 2-Chloro-1-(3,4-dimethyl-phenyl)-ethanone, Ethanone, 2-Chloro-1-(3,4-Dimethylphenyl)-

Ethanone, 2-chloro-1-(3,4-dimethylphenyl)- (9CI)

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CAS 50690-08-9: 2-chloro-1-(3,4-dimethylphenyl)ethanone

Ethanone, 2-chloro-1-(3,4-dimethylphenyl)- (9CI)

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2-chloro-1-(3,4-dimethylphenyl)-1-ethanone

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2-chloro-1-(3,4-dimethylphenyl)ethanone

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2-Chloro-1-(3,4-Dimethylphenyl)Ethanone

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