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1-Bromo-2,6-dicyanobenzene, with the molecular formula C8H3BrN2, is a brominated derivative of dicyanobenzene and is classified as a halogenated aromatic compound. It is known for its strong electron-withdrawing properties and is commonly used as a building block in organic synthesis.

22433-90-5

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22433-90-5 Usage

Uses

Used in Organic Synthesis:
1-Bromo-2,6-dicyanobenzene is used as a building block in organic synthesis for its strong electron-withdrawing properties, which make it a valuable compound in the field of organic chemistry.
Used in Pharmaceutical Production:
1-Bromo-2,6-dicyanobenzene is used as a key intermediate in the production of pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Manufacturing:
This chemical compound is utilized in the manufacturing of agrochemicals, playing a role in the development of pesticides and other agricultural chemicals to improve crop protection and yield.
Used in Dyes and Pigments Industry:
1-Bromo-2,6-dicyanobenzene is used as a starting material in the production of dyes and pigments, contributing to the creation of a wide range of colorants for various applications, including textiles, plastics, and inks.

Check Digit Verification of cas no

The CAS Registry Mumber 22433-90-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,3 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22433-90:
(7*2)+(6*2)+(5*4)+(4*3)+(3*3)+(2*9)+(1*0)=85
85 % 10 = 5
So 22433-90-5 is a valid CAS Registry Number.

22433-90-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Bromoisophthalonitrile

1.2 Other means of identification

Product number -
Other names 1-bromo-2,6-dicyanobenzene

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:22433-90-5 SDS

22433-90-5Relevant academic research and scientific papers

Functionalizations of Mixtures of Regioisomeric Aryllithium Compounds by Selective Trapping with Dichlorozirconocene

Castell-Mic, Alicia,Herbert, Simon A.,Len, Thierry,Bein, Thomas,Knochel, Paul

supporting information, p. 401 - 404 (2016/01/25)

The reaction of mixtures of aryllithium regioisomers obtained either by directed lithiation or by Br/Li exchange with substoichiometric amounts of Cp2ZrCl2 proceeds with high regioselectivity. The least sterically hindered regioisome

Modulation of (non)linear optical properties in tripodal molecules by variation of the peripheral cyano acceptor moieties and the π-spacer

Cvejn,Michail,Polyzos,Almonasy,Pytela,Klikar,Mikysek,Giannetas,Fakis,Bure

supporting information, p. 7345 - 7355 (2015/08/11)

A series of twelve tripodal push-pull molecules with a central triphenylamine donor and peripheral cyano substituted acceptors has been prepared. These molecules possess systematically altered π-linkers as well as cyano acceptors. Based on the experimental properties measured by differential scanning calorimetry, electrochemistry, one and two photon absorption/emission spectroscopy, supported by the DFT calculations, thorough structure-property relationships were elucidated.

Directed Ortho Lithiation of Isophthalonitrile. New Methodology for the Synthesis of 1,2,3-Trisubstituted Benzenes

Krizan, Timothy D.,Martin, J. C.

, p. 2681 - 2682 (2007/10/02)

The lithiation of 1,3-dicyanobenzene with lithium diisopropylamide occurs in high yield, regiospecifically at the 2-position, to give aryllithium species stable at temperatures below -90 deg C.

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