206268-72-6

Basic information

• Product Name: 1,2-Benzenedicarbonitrile, 4-bromo-5-nitro-
• CAS NO: 206268-72-6
• Molecular Formula: C8H2BrN3O2
• Molecular Weight: 252.027
• Mol File: 206268-72-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,2-Benzenedicarbonitrile, 4-bromo-5-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Benzenedicarbonitrile, 4-bromo-5-nitro-(206268-72-6)
• EPA Substance Registry System: 1,2-Benzenedicarbonitrile, 4-bromo-5-nitro-(206268-72-6)

Safety Data

• Hazardous Substances Data: 206268-72-6(Hazardous Substances Data)

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

Describes the physical appearance of the compound, which is yellow in color and has a crystalline structure.

Explanation

The compound is often used as a starting material or intermediate in the synthesis of other organic compounds.

Explanation

It is widely utilized in the pharmaceutical industry for the preparation of various pharmaceutical drugs.

Explanation

The compound has functional groups that allow it to participate in various chemical reactions, making it versatile in its applications.

Explanation

It is often used as a building block in the synthesis of complex organic molecules due to its unique structure and properties.

Explanation

The compound has applications in the production of specialty chemicals and agrochemicals, which are chemicals used in specific industries or for specific purposes.

Explanation

Its unique structure and properties make it a valuable and important chemical in the field of organic chemistry, which is the study of carbon-based compounds.

Appearance

Yellow crystalline solid

Common use

Intermediate in organic synthesis

Application

Pharmaceutical industry

Versatile reactivity

Functional groups

Building block

Synthesis of complex organic molecules

Applications

Specialty chemicals and agrochemicals

Importance

Field of organic chemistry

Upstream product

• 64823-14-9 5-bromo-6-nitro-isoindole-1,3-dione 
• 6941-75-9 5-Bromoisoindoline-1,3-dione 

Downstream Products

• 329326-23-0 4-(1-naphthyloxy)-5-nitrophthalodinitrile 
• 115753-34-9 4-amino-5-bromophthalodinitrile 
• 357617-32-4 bis(2-nitro-4,5-dicyanophenyl)sulfide 
• 274924-66-2 4-morpholino-5-nitrophthalinonitrile 
• 356078-31-4 5-nitro-4-(4-nitrophenoxy)phthalodinitrile 
• 492447-33-3 4-(1-benzotriazolyl)-5-hydroxyphthalonitrile 
• 274924-71-9 4-(1H-1,2,3-benzotriazol-1-yl)-5-nitrophthalonitrile 
• 492447-02-6 4-(1-benzotriazolyl)-5-phenoxyphthalonitrile 
• 492447-06-0 4-benzotriazol-1-yl-5-(4-bromo-phenoxy)-phthalonitrile 
• 492447-18-4 4-benzotriazol-1-yl-5-(4-chloro-3-methyl-phenoxy)-phthalonitrile 
• 492447-09-3 4-(1-benzotriazolyl)-5-(4-phenylphenoxy)phthalonitrile 
• 492447-16-2 4-benzotriazol-1-yl-5-(4-chloro-3,5-dimethyl-phenoxy)-phthalonitrile 
• 492447-08-2 4-(1-benzotriazolyl)-5-{[4'-methyl(1,1'-biphenyl)-4-yl]oxy}phthalonitrile 

Relevant articles and documents

Novel azo dye compound

A compound represented by formula (I): Formula (I) wherein Z1 and Z2 each are atoms necessary for forming an aromatic ring; V1 and V2 each are a substituent W1 or W2; when at least one V1 is W1, at least one V2 is W2, or when at least one V1 is W2, at least one V2 is W1; r is 1 to 4; s is 1 to 4; M1 is a counter ion; m1 is the number necessary for neutralizing charge; W1 is a hydroxyl, primary- or secondary- or tertiary-amino, acylamino, or sulfonamido group; W2 is a nitro, cyano, alkoxycarbonyl, aryloxycarbonyl, alkyl- or aryl-sulfonyl, carbamoyl, sulfamoyl, alkenyl, alkynyl, aryl, heterocyclic, sulfo, carboxyl, heterocyclic oxy, ammonio, alkyl- or aryl-sulfinyl, alkyl- or aryl-sulfonyl, acyl, or aryl- or heterocyclic-azo group; and the aromatic ring may have a substituent other than V1 and V2.