4-Chloro-N-methyl-2-nitrobenzenamine, with the CAS number 15950-17-1, is an organic compound that belongs to the class of aromatic amines. It features a benzene ring substituted with a chlorine atom, a nitro group, and a methylamino group. The presence of the nitro group introduces significant polarity and can influence the compound's reactivity, making it a potential candidate for various chemical reactions, including electrophilic substitution. The chlorine atom contributes to the compound's electron-withdrawing properties, which can affect its overall stability and solubility in different solvents. This compound is typically characterized by its yellow to orange crystalline appearance and may exhibit moderate toxicity, necessitating careful handling. Its applications can range from use in dyes and pigments to intermediates in the synthesis of pharmaceuticals and agrochemicals. As with many nitro-substituted compounds, it may also undergo reduction reactions, leading to the formation of amines, which can further expand its utility in organic synthesis.

Benzenamine, 4-chloro-N-methyl-2-nitro-

15950-17-1: 4-Chloro-N-methyl-2-nitrobenzenamine, with the CAS number 15950-17-1, is an organic compound that belongs to the class of aromatic amines. It features a benzene ring substituted with a chlorine atom, a nitro group, and a methylamino group. The presence of the nitro group introduces significant polarity and can influence the compound's reactivity, making it a potential candidate for various chemical reactions, including electrophilic substitution. The chlorine atom contributes to the compound's electron-withdrawing properties, which can affect its overall stability and solubility in different solvents. This compound is typically characterized by its yellow to orange crystalline appearance and may exhibit moderate toxicity, necessitating careful handling. Its applications can range from use in dyes and pigments to intermediates in the synthesis of pharmaceuticals and agrochemicals. As with many nitro-substituted compounds, it may also undergo reduction reactions, leading to the formation of amines, which can further expand its utility in organic synthesis.

CAS 15950-17-1

Benzenamine, 4-chloro-N-methyl-2-nitro-

Benzenamine, 4-chloro-N-methyl-2-nitro-

Ref: IN-DA001R4M

N-Methyl 4-chloro-2-nitroaniline

Ref: 54-OR9445

4-Chloro-N-methyl-2-nitroaniline

Ref: 10-F328934