40932-71-6

Basic information

• Product Name: 4-Bromo-N-(4-nitrophenyl)benzenamine
• Synonyms: 4-Bromo-4'-nitrodiphenylamine;4-Bromo-N-(4-nitrophenyl)benzenamine;4-bromo-N-(4-nitrophenyl)aniline
• CAS NO: 40932-71-6
• Molecular Formula: C₁₂H₉BrN₂O₂
• Molecular Weight: 293.12
• Mol File: 40932-71-6.mol
• Article Data: 2

Chemical Properties

• Melting Point: 162-163 ºC
• Appearance: /
• Density: 1.597
• CAS DataBase Reference: 4-Bromo-N-(4-nitrophenyl)benzenamine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Bromo-N-(4-nitrophenyl)benzenamine(40932-71-6)
• EPA Substance Registry System: 4-Bromo-N-(4-nitrophenyl)benzenamine(40932-71-6)

Safety Data

• Hazardous Substances Data: 40932-71-6(Hazardous Substances Data)

Upstream product

• 589-87-7 1,4-bromoiodobenzene 
• 100-01-6 4-nitro-aniline 
• 91-22-5 quinoline 
• 7664-93-9 sulfuric acid 
• 836-30-6 4-ntrophenyl(phenyl)amine 
• 7726-95-6 bromine 
• 64-19-7 acetic acid 
• 110-86-1 pyridine 

Downstream Products

• 51363-91-8 4-bromo-N-methyl-N-(4-nitrophenyl)aniline 

Relevant articles and documents

Ligand-Enabled Gold-Catalyzed C(sp2)-N Cross-Coupling Reactions of Aryl Iodides with Amines

The first example of ancillary (P,N)-ligand-enabled gold-catalyzed C-N cross-coupling reactions of aryl iodides with amines is reported. The high generality of the reaction in de novo synthesis, late-stage modifications, and cascade processes to access functionalized indolinones and carbazoles underscores the synthetic potential of the presented strategy. Monitoring the reaction with ESI-HRMS and NMR provided strong evidence for the in situ formation of putative high valent Au(III) intermediates.