96558-80-4

Basic information

• Product Name: Benzene, 1,2-dibromo-3,5-dinitro-
• Synonyms: Benzene,1,2-dibromo-3,5-dinitro
• CAS NO: 96558-80-4
• Molecular Formula: C6H2Br2N2O4
• Molecular Weight: 325.901
• Mol File: 96558-80-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, 1,2-dibromo-3,5-dinitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,2-dibromo-3,5-dinitro-(96558-80-4)
• EPA Substance Registry System: Benzene, 1,2-dibromo-3,5-dinitro-(96558-80-4)

Safety Data

• Hazardous Substances Data: 96558-80-4(Hazardous Substances Data)

Upstream product

• 5411-50-7 3,4-dibromonitrobenzene 
• 26429-41-4 1,2-dibromo-3-nitrobenzene 
• 583-53-9 2,3-dibromobenzene 
• 99-65-0 meta-dinitrobenzene 
• 584-48-5 2,4-dinitrobromobenzene 
• 7664-93-9 sulfuric acid 
• 7697-37-2 nitric acid 
• 586-78-7 para-nitrophenyl bromide 
• 97-02-9 2,4-Dinitroanilin 
• 1817-73-8 2-bromo-4,6-dinitroaniline 

Downstream Products

• 1372548-03-2 (2-bromo-4,6-dinitro-phenyl)thiocyanate 
• 1372548-42-9 ethyl 1-[5-[7-cyclohexyl-2-(ethylcarbamoylamino)-1,3-benzothiazol-5-yl]pyrimidin-2-yl]-4-methyl-piperidine-4-carboxylate 
• 1372544-52-9 1-{5-[7-Cyclohexyl-2-(3-ethyl-ureido)-benzothiazol-5-yl]-pyrimidin-2-yl}-4-methyl-piperidine-4-carboxylic acid 
• 1817-73-8 2-bromo-4,6-dinitroaniline 
• 33786-90-2 5‐bromobenzene‐1,3‐diamine 
• 55215-57-1 1-amino-3-bromo-5-nitrobenzene 
• 62827-44-5 6-bromo-2,4-dinitrobenzonitrile 

Relevant articles and documents

Antibacterial Compounds

The present invention provides a compound of the following formula, salts, racemates, diastereomers, enantiomers, esters, carbamates, phosphates, sulfates, deuterated forms and prodrugs thereof. Also provided is the use of these compounds as antibacterials, compositions comprising them and processes for their manufacture.

BROMINATION OF DEACTIVATED AROMATIC COMPOUNDS

Unreactive aromatic compounds can be brominated with high yields by the action of bromine and nitric acid or another oxidizing agent (iodic acid, hydrogen peroxide, etc.) in concentrated sulfuric acid or oleum.Bromination in the presence of nitric acid has lower substrate selectivity than the concurrent nitration.Moderately deactivated aromatic substrates are nitrated initially, whereas inactive substrates are brominated.It is suggested that the electrophilic brominating agent is sulfohypobromite in the form of a complex with sulfuric acid.