30124-19-7

Usage

Uses

Used in Pharmaceutical Industry:
2,6-Dichloro-N-(4-Methoxyphenyl) Benzenamine is used as an intermediate for the synthesis of various pharmaceuticals. It plays a crucial role in the development of new drugs and medicines.
Used in Agrochemical Industry:
2,6-Dichloro-N-(4-Methoxyphenyl) Benzenamine is also used as an intermediate in the production of agrochemicals. It contributes to the development of effective pesticides and other agricultural chemicals.
Safety Precautions:
2,6-Dichloro-N-(4-Methoxyphenyl) Benzenamine is considered to be a hazardous chemical. Due to its potential health and environmental impacts, it should be handled with proper safety precautions.

InChI:InChI=1/C13H11Cl2NO/c1-17-10-7-5-9(6-8-10)16-13-11(14)3-2-4-12(13)15/h2-8,16H,1H3

Upstream product

• 696-62-8 para-iodoanisole 
• 608-31-1 2,6-Dichloroaniline 
• 3776-30-5 2,2,6,6-tetrachlorocyclohexanone 
• 104-94-9 4-methoxy-aniline 
• 19393-92-1 1-bromo-2,6-dichlorobenzene 
• 100-17-4 para-methoxynitrobenzene 
• 100-02-7 4-nitro-phenol 
• 207395-01-5 N-(p-methoxyphenyl)-2,2,6,6-tetrachlorocyclohexaneimine 

Downstream Products

• 207395-03-7 N-(chloroacetyl)-2',6'-(dichlorophenyl)-4-(methoxyphenyl)amine 
• 30118-47-9 <2-(2,6-Dichlor-anilino)-5-methoxy-phenyl>-essigsaeure 
• 69002-84-2 2-(2-((2,6-dichlorophenyl)amino)-5-hydroxyphenyl)acetic acid 
• 1285680-62-7 C₁₅H₁₃Cl₂NO₃ 
• 698357-75-4 N-(chloroacetyl)-2',6'-(dichlorophenyl)-4-(hydroxyphenyl)amine 
• 30267-40-4 1-(2',6'-dichlorophenyl)-1,3-dihydro-5-hydroxyindol-2-one 

Relevant academic research and scientific papers

MATERIALS FOR ORGANIC ELECTROLUMINESCENT DEVICES

The present invention relates to compounds suitable for use in electronic devices, and to electronic devices, especially organic electroluminescent devices, comprising these compounds.

Diclofenac derivatives with insulin-sensitizing activity

A series of diclofenac derivatives were synthesized. The insulin-sensitizing activity of 28 new compounds was evaluated in 3T3-L1 cells. The compounds 10a and 10f exhibited similar insulin-sensitizing activity with positive drug rosiglitazone.

Syntheses and characterization of the acyl glucuronide and hydroxy metabolites of diclofenac

In humans, metabolism of the commonly used nonsteroidal antiinflammatory drug diclofenac 1 yields principally the 4′-hydroxy 2, 5-hydroxy 3, and acyl glucuronide 4 metabolites. All three metabolites have been implicated in rare idiosyncratic adverse react