4-(Butan-2-yloxy)-3-chloro-5-methoxybenzaldehyde, with the CAS number 872183-59-0, is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group. This compound features a chloro substituent at the 3-position and a methoxy group at the 5-position of the benzene ring, along with a butan-2-yloxy group at the 4-position. The presence of these functional groups contributes to its chemical reactivity and potential applications in organic synthesis. The butan-2-yloxy group enhances its solubility in organic solvents, while the chloro and methoxy groups can influence its electronic properties and reactivity. This compound may be of interest in medicinal chemistry and material science due to its unique structural features. Additionally, its synthesis and characterization would typically involve standard organic reactions, including nucleophilic substitutions and functional group transformations. As with many organic compounds, safety precautions should be observed when handling this substance, as it may pose health risks or environmental hazards.

4-(butan-2-yloxy)-3-chloro-5-methoxybenzaldehyde

872183-59-0: 4-(Butan-2-yloxy)-3-chloro-5-methoxybenzaldehyde, with the CAS number 872183-59-0, is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group. This compound features a chloro substituent at the 3-position and a methoxy group at the 5-position of the benzene ring, along with a butan-2-yloxy group at the 4-position. The presence of these functional groups contributes to its chemical reactivity and potential applications in organic synthesis. The butan-2-yloxy group enhances its solubility in organic solvents, while the chloro and methoxy groups can influence its electronic properties and reactivity. This compound may be of interest in medicinal chemistry and material science due to its unique structural features. Additionally, its synthesis and characterization would typically involve standard organic reactions, including nucleophilic substitutions and functional group transformations. As with many organic compounds, safety precautions should be observed when handling this substance, as it may pose health risks or environmental hazards.

CAS 872183-59-0

4-(butan-2-yloxy)-3-chloro-5-methoxybenzaldehyde

4-sec-butoxy-3-chloro-5-methoxybenzaldehyde

Ref: 10-F315012