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3-Chloro-4-[(3,4-dichlorophenyl)methoxy]benzenamine is a chemical compound that includes elements such as chlorine, hydrogen, carbon, nitrogen, and oxygen in its makeup. It belongs to a class of organic compounds known as diphenylmethanes, particularly to aromatics, due to the presence of a benzene ring in its structure. In terms of functionality, it has an amine group (a basic nitrogen with a lone pair) and an ether group (oxygen atom connected to two alkyl or aryl groups). 3-Chloro-4-[(3,4-dichlorophenyl)methoxy]benzenamine is significant in the chemical industry and is commonly used in organic synthesis. The exact properties, such as color, melting point, boiling point, toxicity, and reactivity, will depend on the environmental factors and the specific chemical context where 3-Chloro-4-[(3,4-dichlorophenyl)methoxy]benzenamine is used.

1039922-08-1

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1039922-08-1 Usage

Uses

Used in Chemical Industry:
3-Chloro-4-[(3,4-dichlorophenyl)methoxy]benzenamine is used as an intermediate in organic synthesis for the production of various chemical products. Its unique structure and functional groups make it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Synthesis:
3-Chloro-4-[(3,4-dichlorophenyl)methoxy]benzenamine is used as a building block in the development of new pharmaceutical compounds. Its amine and ether groups can be further modified to create a wide range of drug candidates with potential therapeutic applications.
Used in Agrochemical Production:
3-Chloro-4-[(3,4-dichlorophenyl)methoxy]benzenamine is used as a key component in the synthesis of agrochemicals, such as pesticides and herbicides. Its chemical properties allow for the creation of effective compounds that can protect crops from pests and diseases.
Used in Specialty Chemicals:
3-Chloro-4-[(3,4-dichlorophenyl)methoxy]benzenamine is used as a raw material in the production of specialty chemicals, such as dyes, fragrances, and polymers. Its versatility in chemical reactions enables the creation of a diverse range of products with specific properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1039922-08-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,9,9,2 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1039922-08:
(9*1)+(8*0)+(7*3)+(6*9)+(5*9)+(4*2)+(3*2)+(2*0)+(1*8)=151
151 % 10 = 1
So 1039922-08-1 is a valid CAS Registry Number.

1039922-08-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-4-[(3,4-dichlorophenyl)methoxy]aniline

1.2 Other means of identification

Product number -
Other names 3-CHLORO-4-[(3,4-DICHLOROPHENYL)METHOXY]BENZENAMINE

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:1039922-08-1 SDS

1039922-08-1Downstream Products

1039922-08-1Relevant academic research and scientific papers

Surmounting the resistance against EGFR inhibitors through the development of thieno[2,3-d]pyrimidine-based dual EGFR/HER2 inhibitors

Milik, Sandra N.,Abdel-Aziz, Amal Kamal,Lasheen, Deena S.,Serya, Rabah A.T.,Minucci, Saverio,Abouzid, Khaled A.M.

, p. 316 - 336 (2018)

In light of the emergence of resistance against the currently available EGFR inhibitors, our study focuses on tackling this problem through the development of dual EGFR/HER2 inhibitors with improved enzymatic affinities. Guided by the binding mode of the

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