(5'-Chloro-2',3'-dimethoxy)acetophenone, with the CAS number 117052-19-4, is an organic compound characterized by its acetophenone structure modified by the presence of a chlorine atom and two methoxy groups. The chlorine substituent is located at the 5' position of the aromatic ring, while the methoxy groups are positioned at the 2' and 3' positions, contributing to the compound's overall polarity and reactivity. This compound typically exhibits a white to off-white crystalline appearance and is soluble in organic solvents, reflecting its hydrophobic aromatic character. Its functional groups suggest potential applications in organic synthesis, particularly in the development of pharmaceuticals or agrochemicals. The presence of the methoxy groups can enhance the compound's electron-donating properties, influencing its reactivity in electrophilic aromatic substitution reactions. Additionally, the chlorine atom may impart unique properties, such as increased lipophilicity or altered biological activity. As with many organic compounds, safety precautions should be observed when handling this substance, as it may pose health risks if ingested or inhaled.

(5'-CHLORO-2',3'-DIMETHOXY)ACETOPHENONE

117052-19-4: (5'-Chloro-2',3'-dimethoxy)acetophenone, with the CAS number 117052-19-4, is an organic compound characterized by its acetophenone structure modified by the presence of a chlorine atom and two methoxy groups. The chlorine substituent is located at the 5' position of the aromatic ring, while the methoxy groups are positioned at the 2' and 3' positions, contributing to the compound's overall polarity and reactivity. This compound typically exhibits a white to off-white crystalline appearance and is soluble in organic solvents, reflecting its hydrophobic aromatic character. Its functional groups suggest potential applications in organic synthesis, particularly in the development of pharmaceuticals or agrochemicals. The presence of the methoxy groups can enhance the compound's electron-donating properties, influencing its reactivity in electrophilic aromatic substitution reactions. Additionally, the chlorine atom may impart unique properties, such as increased lipophilicity or altered biological activity. As with many organic compounds, safety precautions should be observed when handling this substance, as it may pose health risks if ingested or inhaled.

CAS 117052-19-4

(5'-CHLORO-2',3'-DIMETHOXY)ACETOPHENONE

1-(5-Chloro-2,3-dimethoxy-phenyl)-ethanone

Ref: IN-DA000DMH

(5′-CHLORO-2′,3′-DIMETHOXY)ACETOPHENONE

Ref: 10-F302731