2316-50-9

Basic information

• Product Name: 2-bromo-4,6-dinitrophenol
• Synonyms: 2,4-Dinitro-6-bromophenol; 2-Bromo-4,6-dinitrophenol; 6-Bromo-2,4-dinitrophenol; Phenol, 2-bromo-4,6-dinitro-
• CAS NO: 2316-50-9
• Molecular Formula: C₆H₃BrN₂O₅
• Molecular Weight: 263.0024
• Mol File: 2316-50-9.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 302.2°C at 760 mmHg
• Flash Point: 136.6°C
• Density: 2.059g/cm³
• Vapor Pressure: 0.00056mmHg at 25°C
• Refractive Index: 1.691
• CAS DataBase Reference: 2-bromo-4,6-dinitrophenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromo-4,6-dinitrophenol(2316-50-9)
• EPA Substance Registry System: 2-bromo-4,6-dinitrophenol(2316-50-9)

Safety Data

• Hazardous Substances Data: 2316-50-9(Hazardous Substances Data)

Upstream product

• 51-28-5 2,4-Dinitrophenol 
• 19628-79-6 2,6-dibromo-4-nitrosophenol 
• 92874-42-5 2,6,2',6'-tetrabromo-4,4'-sec-butylidene-di-phenol 
• 1817-73-8 2-bromo-4,6-dinitroaniline 
• 7697-37-2 nitric acid 
• 118-79-6 2,4,6-tribromophenol 
• 64-19-7 acetic acid 
• 7664-93-9 sulfuric acid 
• 7693-52-9 4-bromo-2-nitrophenol 
• 15969-09-2 2,4-dibromo-6-nitrophenol 
• 106-41-2 4-bromo-phenol 
• 7732-18-5 water 
• 7726-95-6 bromine 
• 3147-55-5 3,5-dibromosalicylic acid 

Downstream Products

• 55229-71-5 acetic acid-(2-bromo-4,6-dinitro-phenyl ester) 
• 185335-67-5 2-amino-6-bromo-4-nitro-phenol 
• 861362-52-9 N-(2-bromo-4,6-dinitro-phenyl)-hydroxylamine 
• 69399-60-6 3-Bromo-5-nitro-1,2-diaminobenzene 
• 1817-73-8 2-bromo-4,6-dinitroaniline 
• 91330-95-9 (2-bromo-4,6-dinitro-phenyl)-phenyl-amine 
• 26103-32-2 1,3-Dinitro-phenoxazin 
• 860570-86-1 acetic acid-(3-bromo-2-hydroxy-5-nitro-anilide) 
• 475095-97-7 methyl (2-bromo-4,6-dinitrophenylsulphanyl)ethanoate 
• 51796-81-7 1-bromo-2-chloro-3,5-dinitrobenzene 
• 105298-96-2 benzoic acid-(2-bromo-4,6-dinitro-phenyl ester) 
• 36324-64-8 2-Bromo-4,6-dinitroanisole 

Relevant articles and documents

Communications from the Laboratory of the London Institution. On the action of potassic sulphite on the haloid derivatives of phenol

-

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.

Simple and improved regioselective brominations of aromatic compounds using N-benzyl-N,N-dimethylanilinium peroxodisulfate in the presence of potassium bromide under mild reactions conditions

A simple, efficient, and mild method for the selective bromination of some activated aromatic compounds using N-benzyl-N,N-dimethylanilinium peroxodisulfate in the presence of potassium bromide in non-aqueous solution is reported. The results obtained revealed good to excellent selectivity between the ortho and para positions of phenols and methoxyarenes.