2-Chloro-6-nitrobenzenamine, with the CAS number 769-11-9, is an organic compound characterized by the presence of both a chloro and a nitro group attached to a benzene ring, along with an amino group. This compound typically appears as a solid and is known for its pale yellow to brown color. It is classified as an aromatic amine due to the presence of the amino group (-NH2) directly bonded to the benzene ring. The chloro group introduces a halogen, which can influence the compound's reactivity and solubility, while the nitro group (-NO2) is a strong electron-withdrawing group that can affect the compound's electronic properties and reactivity in electrophilic substitution reactions. 2-Chloro-6-nitrobenzenamine is used in various chemical syntheses and may serve as an intermediate in the production of dyes, pharmaceuticals, and agrochemicals. As with many aromatic amines, it is important to handle this compound with care due to potential health hazards associated with amines and nitro compounds.

2-Chloro-6-nitrobenzenamine

769-11-9: 2-Chloro-6-nitrobenzenamine, 6-Chloro-2-nitroaniline, Aniline, 2-chloro-6-nitro-, Benzenamine, 2-chloro-6-nitro-, 2-Chloro-6-nitroaniline

2-Chloro-6-Nitroaniline

2-Chloro-6-nitroaniline

2-Chloro-6-nitroaniline is a compound that is used to synthesize other compounds, such as quinoxalines. It can be obtained by reacting naphthalene with nitric acid in the presence of a proton donor. 2-Chloro-6-nitroaniline has been shown to have a magnetic property when dissolved in an acid solution and has been used as a reagent for the synthesis of azides and anions. The substituent effects on the molecule are significant, which can be seen through its reaction with sodium trifluoroacetate or trifluoroacetic acid. The structure of this compound is also analysed using ionizing techniques.

CAS 769-11-9: 2-Chloro-6-nitrobenzenamine

2-Chloro-6-Nitroaniline

Ref: IN-DA00338Y

2-Chloro-6-nitroaniline

Ref: 54-OR26571

2-Chloro-6-nitroaniline

Ref: 3D-FC15382

2-Chloro-6-nitroaniline

Ref: 10-F044831