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2,6-dichloro-4-toluidine, also known as 2,6-Dichloro-p-toluidine, DCPT, or Dichlofenac, is a chemical compound that typically appears as a pale yellow or off-white crystalline solid. Its appearance may vary depending on the level of purity. 2,6-dichloro-4-toluidine is primarily used in the manufacturing sector for the production of other compounds, such as the pesticide dicamba.

56461-98-4

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56461-98-4 Usage

Uses

Used in Chemical Manufacturing:
2,6-dichloro-4-toluidine is used as a chemical intermediate for the production of various compounds, including the pesticide dicamba. Its role in this application is to serve as a building block in the synthesis process.
Used in Pesticide Production:
2,6-dichloro-4-toluidine is used as a precursor in the manufacturing of dicamba, a widely used herbicide. 2,6-dichloro-4-toluidine is transformed through chemical reactions to produce the final herbicidal product.
However, it is important to note that 2,6-dichloro-4-toluidine 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 to minimize risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 56461-98-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,4,6 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 56461-98:
(7*5)+(6*6)+(5*4)+(4*6)+(3*1)+(2*9)+(1*8)=144
144 % 10 = 4
So 56461-98-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H7Cl2N/c1-4-2-5(8)7(10)6(9)3-4/h2-3H,10H2,1H3

56461-98-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-Dichloro-4-methylaniline

1.2 Other means of identification

Product number -
Other names 2.6-Dichlor-p-toluidin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:56461-98-4 SDS

56461-98-4Relevant academic research and scientific papers

N-Chloro-N-methoxybenzenesulfonamide: A Chlorinating Reagent

Pu, Xiaoqiu,Li, Qingwei,Lu, Zehai,Yang, Xianjin

supporting information, p. 5937 - 5940 (2016/12/26)

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.

CFBSA: a novel and practical chlorinating reagent

Lu, Zehai,Li, Qingwei,Tang, Minghua,Jiang, Panpan,Zheng, Hao,Yang, Xianjin

supporting information, p. 14852 - 14855 (2015/10/06)

A structurally simple, highly reactive chlorinating reagent, N-chloro-N-fluorobenzenesulfonylamine (CFBSA), was conveniently prepared from inexpensive Chloramine B in high yield. A wide range of substrates were chlorinated with it to obtain products in good to high yields and appropriate selectivity.

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

Vyas, Punita V.,Bhatt, Anjani K.,Ramachandraiah, Gadde,Bedekar, Ashutosh V.

, p. 4085 - 4088 (2007/10/03)

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

-

, (2008/06/13)

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

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