105836-68-8

Basic information

• Product Name: Benzenamine, 3,5-dichloro-N-phenyl-
• CAS NO: 105836-68-8
• Molecular Formula: C12H9Cl2N
• Molecular Weight: 238.116
• Mol File: 105836-68-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzenamine, 3,5-dichloro-N-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 3,5-dichloro-N-phenyl-(105836-68-8)
• EPA Substance Registry System: Benzenamine, 3,5-dichloro-N-phenyl-(105836-68-8)

Safety Data

• Hazardous Substances Data: 105836-68-8(Hazardous Substances Data)

Usage

General Description

Benzenamine, 3,5-dichloro-N-phenyl- is a chemical compound that belongs to the class of amines. It is also known by its common name, 3,5-dichloroaniline. Benzenamine, 3,5-dichloro-N-phenyl- is widely used in the production of dyes, agrochemicals, and pharmaceuticals. It is a pale yellow to brown solid with a slightly musty odor. Benzenamine, 3,5-dichloro-N-phenyl- is considered to be toxic if ingested, inhaled, or comes into contact with the skin, and can cause irritation to the eyes, skin, and respiratory system. Therefore, proper safety precautions and handling procedures should be followed when working with this chemical.

Upstream product

• 62-53-3 aniline 
• 77826-12-1 N-(3,5-dichloro-phenyl)-N-phenyl-benzamide 
• 19752-55-7 1-bromo-3,5-dichlorobenzene 
• 103-84-4 Acetanilid 
• 18201-65-5 2-(3,5-dichlorophenylamino)benzoic acid 
• 108-86-1 bromobenzene 
• 31592-84-4 N-(3,5-dichlorophenyl)-acetamide 
• 39943-56-1 3,5-dichlorophenylhydrazine 
• 626-43-7 3,5-Dichloroaniline 
• 16463-38-0 potassium 2-chlorobenzoate 
• 83426-49-7 N-(3,5-dichlorophenyl)benzamide 
• 15999-94-7 N-(3,5-dichlorophenyl)benzimidoyl chloride 

Downstream Products

• 107707-33-5 N-[3,5-dichlorophenyl]thiourea 
• 1427461-88-8 C₁₆H₁₃Cl₂N₃O 

Relevant articles and documents

O-iodoxybenzoic acid mediated N-arylation of aromatic amines by using arylhydrazines as the arylating counterpart

Through free-radical trapping experiments we have established, for the first time, the combination of arylhydrazines with o-iodoxybenzoic acid (IBX) for the generation of aryl free radicals. On the basis of this finding, a method was developed for the N-arylation of aromatic amines under mild conditions (base-free, -5 °C) by using arylhydrazines as the arylating counterpart and arylamines. The scope of this method was demonstrated by using a number of arylhydrazines and arylamines, which gave the N-arylated amines in good yields. Through free-radical trapping experiments, the present work describes the combination of arylhydrazines with o-iodoxybenzoic acid (IBX) for the generation aryl free radicals. This finding is exploited in the development of a mild method for the N-arylation of arylamines by using arylhydrazines as the arylating agents. The scope of this method is demonstrated through a number of examples. Copyright

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