110392-56-8

Basic information

• Product Name: bis(4-nitrobenzyl)phenylamine
• Synonyms: bis(4-nitrobenzyl)phenylamine
• CAS NO: 110392-56-8
• Molecular Weight: 363.373
• Mol File: 110392-56-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: bis(4-nitrobenzyl)phenylamine(CAS DataBase Reference)
• NIST Chemistry Reference: bis(4-nitrobenzyl)phenylamine(110392-56-8)
• EPA Substance Registry System: bis(4-nitrobenzyl)phenylamine(110392-56-8)

Safety Data

• Hazardous Substances Data: 110392-56-8(Hazardous Substances Data)

Upstream product

• 100-14-1 4-nitrobenzyl chloride 
• 62-53-3 aniline 
• 151-21-3 sodium dodecyl-sulfate 
• 100-11-8 1-bromomethyl-4-nitro-benzene 
• 785-80-8 p-nitrobenzylideneaniline 
• 619-73-8 4-nitrobenzyl chloride 

Downstream Products

• 83215-18-3 4-aniline 
• 1252602-02-0 N-(methoxycarbonyl)-3-methyl-L-valyl-N-[4-({phenyl[4-({1-[(2R)-2-phenyl-2-pyrrolidin-1-ylacetyl]-L-prolyl}amino)benzyl]amino}methyl)phenyl]-L-prolinamide 
• 1252602-31-5 methyl R-2-oxo-1-phenyl-2-((S)-2-(4-((phenyl(4-((S)-pyrrolidine-2-carboxamido)benzyl)amino)methyl)phenylcarbamoyl)pyrrolidin-1yl)ethylcarbamate 
• 1252600-83-1 methyl (S)-1-((S)-2-(4-(((4-((S)-1-((R)-2-(dimethylamino)-2-phenylacetyl)pyrrolidine-2-carboxamido)benzyl)(phenyl)amino)methyl)phenylcarbamoyl)pyrrolidin-1-yl)-3,3-dimethyl-1-oxobutan-2-ylcarbamate 
• 1252600-84-2 methyl (S)-3,3-dimethyl-1-oxo-1-((S)-2-(4-((phenyl(4-((S)-pyrrolidine-2-carboxamido)benzyl)amino)methyl)phenylcarbamoyl)pyrrolidin-1-yl)butan-2-ylcarbamate 
• 1252600-86-4 methyl (S)-1-((S)-2-(4-(((4-((S)-1-((R)-2-(diethylamino)-2-phenylacetyl)pyrrolidine-2-carboxamido)benzyl)(phenyl)amino)methyl)phenylcarbamoyl)pyrrolidin-1-yl)-3,3-dimethyl-1-oxobutan-2-ylcarbamate 

Relevant articles and documents

Regioselective Synthesis of 2° Amides Using Visible-Light-Induced Photoredox-Catalyzed Nonaqueous Oxidative C-N Cleavage of N, N-Dibenzylanilines

A visible-light-driven photoredox-catalyzed nonaqueous oxidative C-N cleavage of N,N-dibenzylanilines to 2° amides is reported. Further, we have applied this protocol on 2-(dibenzylamino)benzamide to afford quinazolinones with (NH4)2S2O8 as an additive. Mechanistic studies imply that the reaction might undergo in situ generation of α-amino radical to imine by C-N bond cleavage followed by the addition of superoxide ion to form amides.

ANTI-VIRAL COMPOUNDS

Compounds effective in inhibiting replication of Hepatitis C virus (“HCV”) are described. This invention also relates to processes of making such compounds, compositions comprising such compounds, and methods of using such compounds to treat HCV infection.

Anti-Viral Compounds

Compounds effective in inhibiting replication of Hepatitis C virus (“HCV”) are described. This invention also relates to processes of making such compounds, compositions comprising such compounds, and methods of using such compounds to treat HCV infection.