Home Chemistry Organic Building Blocks Amines N,N-Diphenyl-[1,1'-Biphenyl]-4-Amine
Nitration: Diphenylamine can be nitrated to form N-phenyl-4-nitrodiphenylamine, which is used as an intermediate in the synthesis of dyes and pigments.
Friedel-Crafts Acylation: It can undergo Friedel-Crafts acylation reactions, resulting in the introduction of acyl groups (RCO-) onto the amino group
Azo Coupling: Diphenylamine can undergo azo coupling reactions to form azo dyes by reacting with diazonium salts of aromatic amines.
Mannich Reaction: It can participate in the Mannich reaction, where it reacts with formaldehyde and a primary or secondary amine to form a β-amino ketone or aldehyde.
Halogenation: Diphenylamine can be halogenated by reaction with various halogenating agents to introduce halogen atoms (e.g., chlorine or bromine) onto the aromatic rings.
Alkylation: It can be alkylated to introduce alkyl groups onto the amino or aromatic rings.
Formation of Derivatives: Various derivatives of diphenylamine can be synthesized, including Schiff bases, imines, and other compounds through condensation reactions.
Formation of Coordination Compounds: Diphenylamine can form coordination compounds with various metal ions, making it suitable for various analytical and synthetic applications
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4'-Bromo-N,N-diphenyl-[1,1'-biphenyl]-4-amine
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4'-(Diphenylamino)-[1,1'-biphenyl]-4-carbaldehyde
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4'-(Diphenylamino)-3-hydroxy-[1,1'-biphenyl]-4-carbaldehyde
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(4-([1,1'-Biphenyl]-4-yl(phenyl)amino)phenyl)boronic acid
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N-(4-Bromophenyl)-N-phenyl-[1,1'-biphenyl]-4-amine
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N-(3-Bromophenyl)-N-phenyl-[1,1'-biphenyl]-4-amine
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2-(4'-(Diphenylamino)-[1,1'-biphenyl]-4-yl)acetonitrile
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