3-Amino-4-chlorobenzaldehyde is an organic compound characterized by the presence of an amino group (-NH2) and a chlorobenzaldehyde functional group on a benzene ring. Its molecular structure consists of a benzene ring substituted with an amino group at the meta position (3-position) and a chlorobenzaldehyde group at the para position (4-position). This compound is typically a solid at room temperature and may exhibit a pale yellow to off-white appearance. It is soluble in polar organic solvents, such as ethanol and dimethyl sulfoxide, but has limited solubility in non-polar solvents. The presence of both the amino and aldehyde functional groups allows for potential reactivity in various chemical reactions, including nucleophilic substitutions and condensation reactions. 3-Amino-4-chlorobenzaldehyde can be utilized in the synthesis of pharmaceuticals, agrochemicals, and dyes, making it a valuable intermediate in organic synthesis. Additionally, it may exhibit biological activity, which can be explored in medicinal chemistry.

3-amino-4-chlorobenzaldehyde

77740-83-1: 3-Amino-4-chlorobenzaldehyde is an organic compound characterized by the presence of an amino group (-NH2) and a chlorobenzaldehyde functional group on a benzene ring. Its molecular structure consists of a benzene ring substituted with an amino group at the meta position (3-position) and a chlorobenzaldehyde group at the para position (4-position). This compound is typically a solid at room temperature and may exhibit a pale yellow to off-white appearance. It is soluble in polar organic solvents, such as ethanol and dimethyl sulfoxide, but has limited solubility in non-polar solvents. The presence of both the amino and aldehyde functional groups allows for potential reactivity in various chemical reactions, including nucleophilic substitutions and condensation reactions. 3-Amino-4-chlorobenzaldehyde can be utilized in the synthesis of pharmaceuticals, agrochemicals, and dyes, making it a valuable intermediate in organic synthesis. Additionally, it may exhibit biological activity, which can be explored in medicinal chemistry.

CAS 77740-83-1

3-amino-4-chlorobenzaldehyde