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2,6-difluorobenzene-1,4-diamine is an organic compound with the molecular formula C6H6F2N2. It is a derivative of benzene, featuring two fluorine atoms at the 2nd and 6th positions and two amino groups at the 1st and 4th positions. 2,6-difluorobenzene-1,4-diamine is known for its unique electronic properties due to the presence of fluorine atoms, which can influence its reactivity and stability. It is used in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals, where its fluorinated nature can impart specific biological activities or improve the compound's metabolic stability. The compound is also of interest in materials science for the development of new polymers and other advanced materials.

3743-86-0

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3743-86-0 Usage

Structure

A benzene ring with two amino groups (-NH2) and two fluorine atoms (-F) as substituents.

Derivative

It is a derivative of benzene.

Usage

Commonly used in the production of dyes and pigments.

Building Block

A useful building block for the synthesis of various organic compounds due to its aromatic diamine nature.

Industrial Applications

Used in the manufacturing of polyurethane and epoxy resins.

Additional Applications

Employed in the production of pharmaceuticals and agrochemicals.

Hazardous Exposure

Exposure to 2,6-difluorobenzene-1,4-diamine can be hazardous.

Precautions

Proper safety measures should be taken when handling this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 3743-86-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,4 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3743-86:
(6*3)+(5*7)+(4*4)+(3*3)+(2*8)+(1*6)=100
100 % 10 = 0
So 3743-86-0 is a valid CAS Registry Number.

3743-86-0SDS

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 2,6-difluorobenzene-1,4-diamine

1.2 Other means of identification

Product number -
Other names 2,6-Difluoro-p-phenylenediamine

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:3743-86-0 SDS

3743-86-0Relevant academic research and scientific papers

Catalytic and noncatalytic ammonolysis of polyfluorinated 1,3-dichlorobenzenes

Selivanova,Pokrovskii,Shteingarts

, p. 1023 - 1029 (2007/10/03)

Reactions of 1,3-dichlorotetrafluorobenzene and 1,3-dichloro-2,4,6-trifluorobenzene with aqueous ammonia in the presence and in the absence of copper(I) salt lead to fluorine replacement by amino group in the para and ortho positions with respect to the chlorine atom. Ammonolysis of the resulting chloropolyfluoroanilines in the absence of a catalyst involves replacement of fluorine atom in the meta position with respect to the amino group. In the presence of copper(I) salt, catalytic aminodechlorination occurs at the para and ortho positions with respect to the amino group introduced in the first stage.

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