Home Chemistry Organic Building Blocks Amines Tri([1,1'-Biphenyl]-4-Yl)Amine
Redox Reactions: TPA is capable of undergoing redox reactions due to the presence of the nitrogen atom. It can be both oxidized and reduced.
Cross-Coupling Reactions: TPA can participate in various cross-coupling reactions, where it can form bonds with other compounds. For instance, Suzuki, Heck, or Sonogashira reactions.
Metalation Reactions: The nitrogen atom in TPA can coordinate with various metal ions, leading to the formation of metal complexes.
Grignard Reactions: TPA can react with Grignard reagents to form new compounds.
Oxidative Coupling: Under certain conditions, TPA can undergo oxidative coupling reactions to form dimers or oligomers.
Substitution Reactions: The hydrogen atoms on the biphenyl rings can be replaced with various functional groups through substitution reactions.
Amination Reactions: TPA can undergo amination reactions to introduce amino groups.
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N,N-Di([1,1'-biphenyl]-4-yl)-4'-bromo-[1,1'-biphenyl]-4-amine
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4',4''',4'''''-Nitrilotris(([1,1'-biphenyl]-3-carboxylic acid))
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4',4''',4'''''-Nitrilotris(([1,1'-biphenyl]-3,5-dicarbaldehyde))
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[1,1-Biphenyl]-4-carboxaldehyde, 4-[bis(4-formyl[1,1-biphenyl]-4-yl)amino]-
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4',4''',4'''''-Nitrilotris(([1,1'-biphenyl]-4-carbonitrile))
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N4,N4-Bis(4'-amino-[1,1'-biphenyl]-4-yl)-[1,1'-biphenyl]-4,4'-diamine
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4,4'',4''''-Nitrilotris(([1,1'-biphenyl]-3,5-dicarboxylic acid))
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