26429-41-4

Basic information

• Product Name: 1,2-DibroMo-3-nitrobenzene
• Synonyms: 1,2-DibroMo-3-nitrobenzene
• CAS NO: 26429-41-4
• Molecular Formula: C₆H₃Br₂NO₂
• Molecular Weight: 280.90152
• Mol File: 26429-41-4.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1,2-DibroMo-3-nitrobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-DibroMo-3-nitrobenzene(26429-41-4)
• EPA Substance Registry System: 1,2-DibroMo-3-nitrobenzene(26429-41-4)

Safety Data

• Hazardous Substances Data: 26429-41-4(Hazardous Substances Data)

Usage

General Description

1,2-Dibromo-3-nitrobenzene is a chemical compound with the molecular formula C6H3Br2NO2. It is a yellow solid that is used in organic synthesis and as an intermediate in the production of dyes and pharmaceuticals. 1,2-DibroMo-3-nitrobenzene is highly reactive and can participate in a variety of chemical reactions, including electrophilic aromatic substitution and nucleophilic aromatic substitution. 1,2-Dibromo-3-nitrobenzene is also flammable and should be handled with care. Its properties make it a valuable tool in the field of organic chemistry, where it is used to create a variety of other chemical compounds with diverse properties and applications.

Upstream product

• 577-19-5 2-nitrophenyl bromide 
• 602-03-9 2,3-dinitroaniline 
• 583-53-9 2,3-dibromobenzene 
• 7697-37-2 nitric acid 
• 615-36-1 2-bromoaniline 
• 10035-10-6 hydrogen bromide 
• 64-19-7 acetic acid 
• 59255-95-7 2-bromo-6-nitroaniline 
• 88-74-4 2-nitro-aniline 

Downstream Products

• 121866-21-5 1-(2-bromo-6-nitrophenyl)heptyne 
• 32337-96-5 1-bromo-2-iodo-3-nitro-benzene 
• 615-55-4 3,4-dibromoaniline 
• 608-22-0 3-amino-1,2-dibromobenzene 
• 90481-68-8 1-bromo-2-ethenyl-3-nitrobenzene 
• 1201561-34-3 4-phenyl-9H-carbazole 
• 121866-23-7 o-n-heptylacetanilide 
• 121866-22-6 2-heptylphenylamine 
• 412041-44-2 2,3-diethynylnitrobenzene 
• 96558-80-4 1,2-dibromo-3,5-dinitrobenzene 
• 3970-37-4 1-bromo-2-chloro-3-nitrobenzene 

Relevant articles and documents

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The synthesis and characterization of nine isomerically defined S-arylmercapturic acids of interest in connection with the metabolism of the model hepatotoxin bromobenzene is described.Included are three S-(bromophenyl)-, two S-(bromohydroxyphenyl)-, and three S-(bromodihydroxyphenyl)mercapturic acids of defined substitution pattern.In addition, several related compounds with two or no bromine atoms are described.These syntheses depend on two basic methods, 1,4-addition of various arene thiols to acetamidoacrylic acid or the 1,4-addition of N-acetyl-L-cysteine to various benzoquinone derivatives.In addition, we describe a method for efficient conversion of the mercapturic acids to thioanisole derivatives, regioisomers of which can be separed and detected at low levels by capillary gas-liquid chromatography.