56461-98-4

Basic information

• Product Name: 2,6-dichloro-4-toluidine
• Synonyms: 2,6-dichloro-4-toluidine;2,6-Dichloro-p-toluidine (NH2=1);2,6-dichloro-4-methylBenzenamine;2,6-Dichloro-p-toluidine
• CAS NO: 56461-98-4
• Molecular Formula: C₇H₇Cl₂N
• Molecular Weight: 176.05
• Mol File: 56461-98-4.mol
• Article Data: 5

Chemical Properties

• Melting Point: 56-57 °C
• Boiling Point: 244.7°Cat760mmHg
• Flash Point: 101.8°C
• Appearance: /
• Density: 1.334g/cm³
• Vapor Pressure: 0.03mmHg at 25°C
• Refractive Index: 1.599
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 1.14±0.10(Predicted)
• CAS DataBase Reference: 2,6-dichloro-4-toluidine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-dichloro-4-toluidine(56461-98-4)
• EPA Substance Registry System: 2,6-dichloro-4-toluidine(56461-98-4)

Safety Data

• Hazardous Substances Data: 56461-98-4(Hazardous Substances Data)

Usage

General Description

2,6-dichloro-4-toluidine is a chemical compound, also known as 2,6-Dichloro-p-toluidine, DCPT or Dichlofenac. It is typically a pale yellow or off-white crystalline solid, however, its appearance might depend on the specific level of purity. This chemical is used for various applications, particularly in the manufacturing sector. In particular, it is used to produce other compounds, such as the pesticide dicamba. However, it is considered hazardous and potentially harmful to the environment and human health. It is moderately toxic if inhaled, ingested, or comes in contact with skin, and can cause damage to organs, the respiratory tract, and the skin. Long term exposure could lead to cancer. Therefore, it should be handled with care and the necessary protective measures should be taken.

InChI:InChI=1/C7H7Cl2N/c1-4-2-5(8)7(10)6(9)3-4/h2-3H,10H2,1H3

Upstream product

• 103-89-9 4-Methylacetanilide 
• 106-49-0 p-toluidine 
• 7647-01-0 hydrogenchloride 
• 7664-93-9 sulfuric acid 
• 18931-78-7 N-(2-chloro-4-methylphenyl)acetamide 
• 99520-03-3 acetic acid-(2,6-dichloro-4-methyl-anilide) 
• 623-11-0 1-methyl-4-nitrosobenzene 

Downstream Products

• 21472-86-6 3,4,5-trichloro-toluene 
• 25186-47-4 3,5-dichlorotoluene 
• 19393-93-2 4-bromo-3,5-dichloro-toluene 
• 939990-12-2 3,5-dichloro-4-iodo-toluene 
• 99520-03-3 acetic acid-(2,6-dichloro-4-methyl-anilide) 
• 4523-44-8 2.6-Dichlor-4-methyl-nitrosobenzol 
• 56461-99-5 1-amidino-3-(2,6-dichloro-4-methylphenyl)urea 
• 1403980-67-5 6-(2,6-dichloro-4-methylphenyl)-5H-pyrrolo[3,4-b]pyrazine-5,7(6H)-dione 
• 1403980-70-0 2-(2,6-dichloro-4-methylphenyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione 
• 1092068-34-2 C₃₂H₃₈Cl₂N₆O₅S 
• 1092069-21-0 C₃₂H₃₆Cl₂N₄O₃ 
• 1092069-74-3 C₂₃H₂₈Cl₂N₄O 
• 1403980-75-5 6-(2,6-dichloro-4-methylphenyl)-5H-dibenzo[c,e]azepine-5,7(6H)-dione 
• 185153-63-3 C₉H₇Cl₅ 

Relevant articles and documents

N-Chloro-N-methoxybenzenesulfonamide: A Chlorinating Reagent

A structurally simple and reactive chlorinating reagent, N-chloro-N-methoxybenzenesulfonamide, was conveniently and economically prepared in high yield. 1,3-Diketones, β-keto esters, benzoyl trifluoroacetones, phenols, anisoles, heteroarenes, and aromatic amines were successfully chlorinated, and the products were obtained in good to high yields.

Environmentally benign chlorination and bromination of aromatic amines, hydrocarbons and naphthols

A simple and efficient procedure for chlorination and bromination of aromatic amines, hydrocarbons and naphthols by the action of aqueous hydrohalic acid and hydrogen peroxide is described. This environmentally clean and safe procedure involves in situ generation of the active halogen and its uncatalyzed reaction with the substrates in this study.

5-amino or substituted amino 1,2,3-triazoles

Novel 5-amino or substituted amino 1,2,3-triazoles are disclosed as having anticoccidial activity. The compounds are useful for controlling coccidiosis when administered in minor quantities to animals, in particular to poultry, usually in admixture with a