2,3,4-Trimethoxy-6-nitrobenzaldehyde is an organic compound characterized by its aromatic structure, featuring a benzaldehyde functional group with three methoxy (-OCH₃) substituents and a nitro (-NO₂) group. The presence of these functional groups contributes to its chemical reactivity and physical properties. Typically, this compound appears as a yellow to orange solid and is soluble in organic solvents such as ethanol and dichloromethane, but may have limited solubility in water due to its hydrophobic methoxy groups. The nitro group introduces electron-withdrawing characteristics, which can influence the compound's reactivity in electrophilic aromatic substitution reactions. Additionally, the methoxy groups can provide electron-donating effects, affecting the overall electronic distribution within the molecule. This compound may be of interest in various fields, including organic synthesis and medicinal chemistry, due to its potential biological activities and applications in the development of pharmaceuticals or agrochemicals. Proper handling and safety measures should be observed, as with all chemical substances, to mitigate any risks associated with its use.

2,3,4-trimethoxy-6-nitrobenzaldehyde

52978-83-3: 2,3,4-Trimethoxy-6-nitrobenzaldehyde is an organic compound characterized by its aromatic structure, featuring a benzaldehyde functional group with three methoxy (-OCH₃) substituents and a nitro (-NO₂) group. The presence of these functional groups contributes to its chemical reactivity and physical properties. Typically, this compound appears as a yellow to orange solid and is soluble in organic solvents such as ethanol and dichloromethane, but may have limited solubility in water due to its hydrophobic methoxy groups. The nitro group introduces electron-withdrawing characteristics, which can influence the compound's reactivity in electrophilic aromatic substitution reactions. Additionally, the methoxy groups can provide electron-donating effects, affecting the overall electronic distribution within the molecule. This compound may be of interest in various fields, including organic synthesis and medicinal chemistry, due to its potential biological activities and applications in the development of pharmaceuticals or agrochemicals. Proper handling and safety measures should be observed, as with all chemical substances, to mitigate any risks associated with its use.

CAS 52978-83-3

2,3,4-trimethoxy-6-nitrobenzaldehyde

2,3,4-Trimethoxy-6-nitrobenzaldehyde

Ref: IN-DA00E2TZ

2,3,4-Trimethoxy-6-nitrobenzaldehyde

Ref: 54-OR1055646

2,3,4-trimethoxy-6-nitrobenzaldehyde

Ref: 10-F374394