7149-14-6

Basic information

• Product Name: 2-Bromo-1-iodo-4-nitrobenzene
• Synonyms: 2-Bromo-1-iodo-4-nitrobenzene
• CAS NO: 7149-14-6
• Molecular Formula: C₆H₃BrINO₂
• Molecular Weight: 327.90199
• Mol File: 7149-14-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 332.7°C at 760 mmHg
• Flash Point: 155°C
• Appearance: /
• Density: 2.349g/cm³
• Vapor Pressure: 0.000276mmHg at 25°C
• Refractive Index: 1.691
• CAS DataBase Reference: 2-Bromo-1-iodo-4-nitrobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Bromo-1-iodo-4-nitrobenzene(7149-14-6)
• EPA Substance Registry System: 2-Bromo-1-iodo-4-nitrobenzene(7149-14-6)

Safety Data

• Hazardous Substances Data: 7149-14-6(Hazardous Substances Data)

Usage

General Description

2-Bromo-1-iodo-4-nitrobenzene is a chemical compound with the molecular formula C6H3BrINO2. It is a nitroaromatic compound with a 2-bromo-1-iodo substitution pattern on the benzene ring. 2-Bromo-1-iodo-4-nitrobenzene is mainly used as a building block in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It is a versatile intermediate that can be used in the synthesis of various organic compounds, including dyes, pigments, and other fine chemicals. It is primarily a reagent in organic chemistry, where it participates in various reactions such as Suzuki-Miyaura cross-coupling, palladium-catalyzed cross-coupling, and other transformation reactions. Additionally, 2-Bromo-1-iodo-4-nitrobenzene is also used in the production of chemical intermediates for the manufacture of electronic materials and specialty chemicals.

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

Upstream product

• 13296-94-1 2-bromo-4-nitroaniline 
• 5411-50-7 3,4-dibromonitrobenzene 
• 614-76-6 N-acetyl-2-bromoaniline 
• 615-36-1 2-bromoaniline 
• 636-98-6 p-nitrobenzene iodide 
• 100-01-6 4-nitro-aniline 

Downstream Products

• 72342-73-5 1-bromo-2-iodo-3,5-dinitro-benzene 
• 13296-94-1 2-bromo-4-nitroaniline 
• 4282-46-6 3-(4'-nitrophenyl)pyridine 
• 57072-72-7 (2-bromo-4,6-dinitro-phenyl)-hydrazine 
• 1616624-68-0 C₂₇H₁₉Br₂NO₂ 
• 1616624-66-8 (E)-1,2-bis(2-bromo-4-nitrophenyl)-1,2-diphenylethene 
• 1240047-96-4 (E)-1-(2-bromo-4-fluorophenyl)-2-(2-bromo-4-nitrophenyl)-1,2-diphenylethene 
• 1616624-45-3 (E)-[2-(2-bromo-4-nitrophenyl)-1-(4-methoxyphenyl)-2-phenylvinyl]trimethylstannane 
• 1616624-46-4 (E)-[2-(2-bromo-4-nitrophenyl)-2-(4-methoxyphenyl)-1-phenylvinyl]-trimethylstannane 
• 1616624-47-5 (E)-1-(2-bromo-4-nitrophenyl)-2-(2-bromo-4-trifluoromethylphenyl)-2-(4-methoxyphenyl)-1-phenylethene 
• 1616624-48-6 (E)-1-(2-bromo-4-nitrophenyl)-2-(2-bromo-4-trifluoro-methylphenyl)-1-(4-methoxyphenyl)-2-phenylethene 
• 1616624-61-3 (E)-[2-(2-bromo-4-nitrophenyl)-1,2-diphenylvinyl]trimethylstannane 

Relevant articles and documents

Rhodium-Catalyzed Synthesis and Optical Properties of Silicon-Bridged Arylpyridines

A convergent and regioselective synthesis of silicon-bridged 4-arylpyridines has been developed through a rhodium-catalyzed [2+2+2] cycloaddition of silicon-containing diynes with nitriles. The absorption and emission properties of these compounds have be

Tribromoisocyanuric acid in trifluoroacetic acid: An efficient system for smooth brominating of moderately deactivated arenes

Moderately deactivated arenes are efficiently brominated by the reaction with tribromoisocyanuric acid (0.34 mol equiv) in trifluoroacetic acid at room temperature in 48-85% isolated yield. This medium avoids the polybromination of the substrate, observed in the same reaction performed in 98% H 2SO4. Georg Thieme Verlag Stuttgart · New York.