63037-63-8

Basic information

• Product Name: 1-Bromo-2-iodo-4-nitrobenzene
• Synonyms: 1-Bromo-2-iodo-4-nitrobenzene;4-Bromo-3-iodonitrobenzene
• CAS NO: 63037-63-8
• Molecular Formula: C₆H₃BrINO₂
• Molecular Weight: 327.90199
• Mol File: 63037-63-8.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 330.6°Cat760mmHg
• Flash Point: 153.8°C
• Appearance: /
• Density: 2.349g/cm³
• Vapor Pressure: 0.000316mmHg at 25°C
• Refractive Index: 1.691
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• CAS DataBase Reference: 1-Bromo-2-iodo-4-nitrobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Bromo-2-iodo-4-nitrobenzene(63037-63-8)
• EPA Substance Registry System: 1-Bromo-2-iodo-4-nitrobenzene(63037-63-8)

Safety Data

• Hazardous Substances Data: 63037-63-8(Hazardous Substances Data)

Usage

Uses

1-Bromo-2-iodo-4-nitrobenzene is used as a reactant in the iodination of deactivated aromatics with N-?iodosuccinimide.

InChI:InChI=1/C6H3BrINO2/c7-5-2-1-4(9(10)11)3-6(5)8/h1-3H

Upstream product

• 586-78-7 para-nitrophenyl bromide 
• 10403-47-1 2-bromo 5-nitroaniline 

Downstream Products

• 63037-64-9 4-bromo-3-iodoaniline 
• 25165-84-8 1-ethyl-5-(4-bromo-3-iodo-phenyl)-biguanide 
• 489409-86-1 2-bromo-5-nitro-1,1'-biphenyl 

Relevant articles and documents

Inducing axial chirality in a "Gel?nder" oligomer by length mismatch of the oligomer strands

Helical molecules are not only esthetically appealing due to their structural beauty, they also display unique physical properties as a result of their chirality.We describe herein a new approach to "Gel?nder" oligomers by interlinking two oligomer strand

Superactive iodination reagent on a base of iodine chloride and silver sulfate

After reaction of ICl and Ag2SO4 in sulfuric acid and separation of resulting AgCl a stable solution is formed, containing very active forms of electrophilic iodine. This solution has a powerful iodination ability with respect to aromatic compounds. Deactivated arenes are iodinated easily and in mild conditions by action of this new reagent in generally good yields of the iodoarenes.

Iodination of Deactivated Aromatics with N-Iodosuccinimide in Trifluoromethanesulfonic Acid (NIS-CF3SO3H) via in Situ Generated Superelectrophile Iodine(I) Trifluoromethanesulfonate

-