3-Chloro-4-(4-chlorophenoxy)aniline

CAS: 24900-79-6

Ref. 3D-ZAA90079

Product Information

• Name: 3-Chloro-4-(4-chlorophenoxy)aniline
• Synonyms: 2,3-Difluorobenzyl Mercaptan, 2,4′-Dichloro-4-aminodiphenyl ether, 2-Chlor-4-amino-phenol-(4-chlor-phenylaether), 2.4'-Dichlor-4-amino-diphenyl-aether, 3-Chlor-4-(4-chlor-phenoxy)-anilin, 3-Chloro-4-(4-Chloro-Phenoxy)-Aniline, 3-Chloro-4-(4-Chlorophenoxy)-Benzenamine, 3-Chloro-4-(p-chlorophenoxy)phenylamine, 3-Chloro-4-p-chlorophenoxyaniline, 4-(4'-Chlorophenoxy)-3-Chloroaniline, 4-Amino-2,4′-dichlorodiphenyl ether, 4-Amino-2-chlorophenyl 4-chlorophenyl ether, 4-Amino-2-chlorophenyl p-chlorophenyl ether, Aniline, 3-chloro-4-(p-chlorophenoxy)-, Benzenamine, 3-chloro-4-(4-chlorophenoxy)-, NSC 14501, NSC 151251, [3-Chloro-4-(4-chlorophenoxy)phenyl]amine

Description

3-Chloro-4-(4-chlorophenoxy)aniline is a versatile compound that has various applications in the field of research and chemical synthesis. It is commonly used as an intermediate in the synthesis of pharmaceuticals, such as dimethyl fumarate, labetalol, statins, fexofenadine, n-acetylmannosamine, ezetimibe, ginsenoside, tnf-α inhibitors, carbamazepine, lithium salts, pioglitazone, and epidermal growth factors.

This compound serves as a building block for the synthesis of these valuable molecules due to its unique chemical properties. Its chloro and phenoxy groups make it highly reactive and capable of undergoing various reactions to form complex organic structures. Researchers and chemists rely on 3-Chloro-4-(4-chlorophenoxy)aniline for its reliability and consistency in producing high-quality intermediates.

In addition to its role in

• Brand: Biosynth

Chemical properties

• Molecular weight: 254.11 g/mol
• Formula: C₁₂H₉Cl₂NO
• Purity: Min. 95%