4-Ethoxy-3-methoxybenzaldehyde oxime is an organic compound characterized by its functional groups, including an aldehyde and an oxime. The presence of the ethoxy and methoxy substituents on the benzene ring contributes to its unique chemical properties, such as solubility and reactivity. This compound typically appears as a crystalline solid and is soluble in organic solvents like ethanol and ether, while being less soluble in water due to its hydrophobic aromatic structure. The oxime functional group, derived from the reaction of the aldehyde with hydroxylamine, imparts specific reactivity, making it useful in various synthetic applications, including the formation of other organic compounds. Additionally, the compound may exhibit biological activity, which can be explored for potential applications in pharmaceuticals or agrochemicals. Its stability and reactivity can be influenced by the electronic effects of the substituents on the aromatic ring, making it a subject of interest in organic synthesis and medicinal chemistry.

4-ethoxy-3-methoxybenzaldehyde oxime

81259-53-2: 4-Ethoxy-3-methoxybenzaldehyde oxime is an organic compound characterized by its functional groups, including an aldehyde and an oxime. The presence of the ethoxy and methoxy substituents on the benzene ring contributes to its unique chemical properties, such as solubility and reactivity. This compound typically appears as a crystalline solid and is soluble in organic solvents like ethanol and ether, while being less soluble in water due to its hydrophobic aromatic structure. The oxime functional group, derived from the reaction of the aldehyde with hydroxylamine, imparts specific reactivity, making it useful in various synthetic applications, including the formation of other organic compounds. Additionally, the compound may exhibit biological activity, which can be explored for potential applications in pharmaceuticals or agrochemicals. Its stability and reactivity can be influenced by the electronic effects of the substituents on the aromatic ring, making it a subject of interest in organic synthesis and medicinal chemistry.

CAS 81259-53-2

4-ethoxy-3-methoxybenzaldehyde oxime

N-[(4-Ethoxy-3-methoxyphenyl)methylidene]hydroxylamine

Ref: 3D-GDA25953