3-Bromo-4-nitrobenzaldehyde is an organic compound characterized by the presence of both a bromine atom and a nitro group attached to a benzaldehyde structure. Its molecular formula typically includes a benzene ring substituted with a bromine atom at the meta position (3-position) and a nitro group at the para position (4-position) relative to the aldehyde functional group. This compound is generally a yellow to orange crystalline solid, exhibiting properties typical of aromatic aldehydes, such as reactivity in nucleophilic addition reactions due to the electrophilic nature of the carbonyl group. The presence of the bromine and nitro substituents can influence its reactivity, making it useful in various synthetic applications, including the preparation of more complex organic molecules. Additionally, 3-bromo-4-nitrobenzaldehyde may exhibit interesting electronic properties due to the electron-withdrawing nature of the nitro group, which can affect its behavior in chemical reactions and interactions with other substances. Safety precautions should be observed when handling this compound, as it may pose health risks.

3-BROMO-4-NITROBENZALDEHYDE

101682-68-2: 3-Bromo-4-nitrobenzaldehyde is an organic compound characterized by the presence of both a bromine atom and a nitro group attached to a benzaldehyde structure. Its molecular formula typically includes a benzene ring substituted with a bromine atom at the meta position (3-position) and a nitro group at the para position (4-position) relative to the aldehyde functional group. This compound is generally a yellow to orange crystalline solid, exhibiting properties typical of aromatic aldehydes, such as reactivity in nucleophilic addition reactions due to the electrophilic nature of the carbonyl group. The presence of the bromine and nitro substituents can influence its reactivity, making it useful in various synthetic applications, including the preparation of more complex organic molecules. Additionally, 3-bromo-4-nitrobenzaldehyde may exhibit interesting electronic properties due to the electron-withdrawing nature of the nitro group, which can affect its behavior in chemical reactions and interactions with other substances. Safety precautions should be observed when handling this compound, as it may pose health risks.

CAS 101682-68-2

3-BROMO-4-NITROBENZALDEHYDE

Benzaldehyde, 3-bromo-4-nitro-

Ref: IN-DA000572

3-Bromo-4-nitrobenzaldehyde

Ref: 54-OR914253

3-Bromo-4-nitrobenzaldehyde

Ref: 10-F048805