22433-90-5

Basic information

• Product Name: 1-bromo-2,6-dicyanobenzene
• Synonyms: 1-bromo-2,6-dicyanobenzene
• CAS NO: 22433-90-5
• Molecular Formula: C₈H₃BrN₂
• Molecular Weight: 207.02682
• Mol File: 22433-90-5.mol
• Article Data: 4

Chemical Properties

• Melting Point: 189-190 °C
• Boiling Point: 322.8±32.0 °C(Predicted)
• Appearance: /
• Density: 1.68±0.1 g/cm3(Predicted)
• CAS DataBase Reference: 1-bromo-2,6-dicyanobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-bromo-2,6-dicyanobenzene(22433-90-5)
• EPA Substance Registry System: 1-bromo-2,6-dicyanobenzene(22433-90-5)

Safety Data

• Hazardous Substances Data: 22433-90-5(Hazardous Substances Data)

Usage

General Description

1-Bromo-2,6-dicyanobenzene is a chemical compound with the molecular formula C8H3BrN2. It is a brominated derivative of dicyanobenzene and is classified as a halogenated aromatic compound. This chemical is commonly used as a building block in organic synthesis and is known for its strong electron-withdrawing properties. It is also utilized in the production of pharmaceuticals and agrochemicals, as well as in the manufacturing of dyes and pigments. Due to its reactivity and versatility, 1-bromo-2,6-dicyanobenzene is a valuable compound in the field of organic chemistry, with numerous applications in industry and research.

Upstream product

• 626-17-5 benzene-1,3-dicarbonitrile 
• 51762-72-2 Benzene-1-nitro-2,6-dicyano 
• 22433-91-6 2-bromoisophthalic acid 
• 576-22-7 2-Bromo-m-xylene 

Downstream Products

• 22433-95-0 2.6-Dicyan-4-nitro-anisol 
• 22433-93-8 2-Methoxi-isophthalonitril 

Relevant articles and documents

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

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

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.