3-Bromo-4-hydroxy-5-nitrobenzaldehyde is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group along with bromine, hydroxy, and nitro substituents. The presence of the bromine atom at the 3-position, a hydroxy group at the 4-position, and a nitro group at the 5-position of the benzene ring contributes to its unique chemical properties and reactivity. This compound is typically a yellow to orange solid and is soluble in organic solvents. It exhibits various functional properties, making it useful in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals. The nitro group is known for its electron-withdrawing effects, which can influence the compound's reactivity in electrophilic aromatic substitution reactions. Additionally, the hydroxy group can participate in hydrogen bonding, affecting solubility and interaction with other molecules. Overall, 3-bromo-4-hydroxy-5-nitrobenzaldehyde serves as an important intermediate in chemical synthesis and research applications.

3-bromo-4-hydroxy-5-nitrobenzaldehyde

98555-49-8: 3-Bromo-4-hydroxy-5-nitrobenzaldehyde is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group along with bromine, hydroxy, and nitro substituents. The presence of the bromine atom at the 3-position, a hydroxy group at the 4-position, and a nitro group at the 5-position of the benzene ring contributes to its unique chemical properties and reactivity. This compound is typically a yellow to orange solid and is soluble in organic solvents. It exhibits various functional properties, making it useful in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals. The nitro group is known for its electron-withdrawing effects, which can influence the compound's reactivity in electrophilic aromatic substitution reactions. Additionally, the hydroxy group can participate in hydrogen bonding, affecting solubility and interaction with other molecules. Overall, 3-bromo-4-hydroxy-5-nitrobenzaldehyde serves as an important intermediate in chemical synthesis and research applications.

CAS 98555-49-8

3-bromo-4-hydroxy-5-nitrobenzaldehyde

3-Bromo-4-hydroxy-5-nitrobenzaldehyde

Ref: IN-DA0067XY

3-bromo-4-hydroxy-5-nitrobenzaldehyde

Ref: 10-F315099