40466-95-3

Basic information

• Product Name: Phenol, 4-bromo-2,6-dinitro-
• Synonyms: Phenol,4-bromo-2,6-dinitro;4-Brom-2,6-dinitro-phenol;2,6-dinitro-4-bromophenol;4-Brom-2.6-dinitro-1-hydroxy-benzol;Phenol, 4-bromo-2,6-dinitro-;4-bromo-2,6-dinitro-phenol
• CAS NO: 40466-95-3
• Molecular Formula: C6H3BrN2O5
• Molecular Weight: 263.004
• Mol File: 40466-95-3.mol
• Article Data: 12

Chemical Properties

• Melting Point: 78°C
• Density: 2.2789 (rough estimate)
• Refractive Index: 1.6100 (estimate)
• CAS DataBase Reference: Phenol, 4-bromo-2,6-dinitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 4-bromo-2,6-dinitro-(40466-95-3)
• EPA Substance Registry System: Phenol, 4-bromo-2,6-dinitro-(40466-95-3)

Safety Data

• Hazardous Substances Data: 40466-95-3(Hazardous Substances Data)

Upstream product

• 7697-37-2 nitric acid 
• 460-00-4 1-Bromo-4-fluorobenzene 
• 106-41-2 4-bromo-phenol 
• 64-19-7 acetic acid 
• 7693-52-9 4-bromo-2-nitrophenol 
• 7664-93-9 sulfuric acid 
• 62554-90-9 4-bromo-2,6-dinitroaniline 
• 64-17-5 ethanol 
• 6310-99-2 2,5-dibromo-1,3-dinitro-benzene 
• 78824-10-9 3,5-dibromosulfanilic acid 
• 67329-16-2 4-hydroxy-3,5-dinitro-benzenesulfonic acid 
• 7732-18-5 water 
• 7726-95-6 bromine 
• 859185-62-9 (4-bromo-phenyl)-(4-methyl-2-nitro-phenyl)-ether 

Downstream Products

• 2316-50-9 2-bromo-4,6-dinitrophenol 
• 139138-08-2 2-amino-4-bromo-6-nitrophenol 
• 88-89-1 2,4,6-Trinitrophenol 
• 67856-76-2 4-bromo-2,6-dinitroanisole 
• 51796-82-8 5-bromo-2-chloro-1,3-dinitro-benzene 

Relevant articles and documents

Nitrogen Oxides and Nitric Acid Enable the Sustainable Hydroxylation and Nitrohydroxylation of Benzenes under Visible Light Irradiation

A new type of waste recycling strategy is described in which nitrogen oxides or nitric acid are directly employed in photocatalyzed hydroxylations and nitrohydroxylations of benzenes. Through these transformations, otherwise costly denitrification can be combined with the synthesis of valuable compounds for various applications.

PEG-N2O4: An efficient nitrating agent for the selective mono- and dinitration of phenols under mild conditions

N2O4 was easily impregnated on polyethyleneglycol to give a stable reagent. The polyethyleneglycol-N2O4 (PEG-N2O4) system was used as an effective nitrating agent for the nitration of phenols. Mono- and dinitrophenols can be obtained via direct nitration of phenols in the presence of PEG-N2O4 at room temperature in moderate to high yields. Copyright Taylor & Francis Group, LLC.

Nitration of aromatic compounds by Zn(NO3)2· 2N2O4 and its charcoal-supported system

Zn(NO3)2·N2O4 and its charcoal supported system were found to be efficient nitrating agents. Mononitration of aromatic compounds such as benzene, alkyl benzenes, halobenzenes, nitrobenzene, anisol, and the highly selective mono-, di-, and trinitration of phenol, and dinitraion of substituted phenols were also performed in the presence of these reagents.