CAS 32407-11-7

Benzenamine, 3,5-dichloro-4-methoxy-

Description:

Benzenamine, 3,5-dichloro-4-methoxy- is an organic compound characterized by its aromatic amine structure, which includes a benzene ring substituted with two chlorine atoms and a methoxy group. The presence of the amine functional group (-NH2) indicates that it can participate in various chemical reactions, such as nucleophilic substitutions. The dichloro substitutions at the 3 and 5 positions of the benzene ring contribute to its reactivity and influence its physical properties, such as solubility and boiling point. The methoxy group (-OCH3) at the 4 position can enhance the compound's electron-donating characteristics, affecting its reactivity and interaction with other chemical species. This compound may be used in various applications, including as an intermediate in the synthesis of dyes, pharmaceuticals, or agrochemicals. Safety considerations should be taken into account, as halogenated compounds can exhibit toxicity and environmental persistence. Proper handling and disposal methods are essential when working with this substance.

Formula: C₇H₇Cl₂NO

Synonyms:

• 3,5-dichloro-4-methoxybenzenamine
• Benzenamine, 3,5-dichloro-4-methoxy-

4-methoxy-3,5-dimethylbenzenamine

CAS: 32407-11-7

Formula: C₇H₇Cl₂NO

Purity: 98%

Color and Shape: Solid

Molecular weight: 192.0426

Ref: IN-DA00CNEK

3,5-Dichloro-4-methoxyaniline

CAS: 32407-11-7

3,5-Dichloro-4-methoxyaniline

Purity: 98%

Molecular weight: 192.04g/mol

Ref: 54-OR92068

3,5-Dichloro-4-methoxyaniline

CAS: 32407-11-7

Purity: 98%

Color and Shape: Solid

Molecular weight: 192.0399933

Ref: 10-F618978

3,5-Dichloro-4-methoxyaniline

CAS: 32407-11-7

3,5-Dichloro-4-methoxyaniline is a chemical compound that belongs to the group of medicinal compounds. It is used as an intermediate in organic synthesis and has been found to inhibit the growth of cancer cells. This molecule can be prepared by reacting 3,5-dichloroaniline with methoxyacetone in the presence of hydrochloric acid. The chemical shifts observed for this compound's proton resonances are consistent with its structure as a geometric isomer. This molecule has two chiral centers and eight possible stereoisomers. Tic10 (N-[3-(3,4-dichlorophenyl)propionyl]glycine) is one such stereoisomer that inhibits the growth of cancer cells through damage to protein structures. Tic10 has been shown to be more potent than bosutinib, an inhibitor of Bcr-Abl kinase, in inhibiting tumor growth in animal models.

Formula: C₇H₇Cl₂NO

Purity: Min. 95%

Molecular weight: 192.04 g/mol

Ref: 3D-HBA40711