Benzaldehyde, 3,4-dinitro- is an aromatic compound characterized by the presence of a benzaldehyde functional group and two nitro groups positioned at the 3 and 4 positions on the benzene ring. Its molecular structure features a carbonyl group (C=O) directly attached to a benzene ring, which is further substituted with nitro groups (–NO2), contributing to its reactivity and properties. This compound is typically a yellow crystalline solid at room temperature and is known for its distinct aromatic odor. It is soluble in organic solvents but has limited solubility in water due to its hydrophobic benzene ring. The presence of nitro groups enhances its electrophilic character, making it a useful intermediate in organic synthesis, particularly in the production of dyes, pharmaceuticals, and other chemical compounds. Additionally, 3,4-dinitrobenzaldehyde exhibits potential biological activity, which may be of interest in medicinal chemistry. As with many nitro compounds, it should be handled with care due to potential toxicity and environmental concerns.

Benzaldehyde, 3,4-dinitro-

35998-98-2: Benzaldehyde, 3,4-dinitro- is an aromatic compound characterized by the presence of a benzaldehyde functional group and two nitro groups positioned at the 3 and 4 positions on the benzene ring. Its molecular structure features a carbonyl group (C=O) directly attached to a benzene ring, which is further substituted with nitro groups (–NO2), contributing to its reactivity and properties. This compound is typically a yellow crystalline solid at room temperature and is known for its distinct aromatic odor. It is soluble in organic solvents but has limited solubility in water due to its hydrophobic benzene ring. The presence of nitro groups enhances its electrophilic character, making it a useful intermediate in organic synthesis, particularly in the production of dyes, pharmaceuticals, and other chemical compounds. Additionally, 3,4-dinitrobenzaldehyde exhibits potential biological activity, which may be of interest in medicinal chemistry. As with many nitro compounds, it should be handled with care due to potential toxicity and environmental concerns.

CAS 35998-98-2

Benzaldehyde, 3,4-dinitro-

3,4-Dinitrobenzaldehyde

Ref: 54-OR303581

3,4-Dinitrobenzaldehyde

Ref: 10-F722218

3,4-Dinitrobenzaldehyde

Ref: TR-D680103