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4',4''',4'''''-nitrilotris(([1,1'-biphenyl]-4-carbaldehyde))

  • CAS No. 872689-79-7

  • Cat. No. CS-0110964
  • Purity≥97%
  • MDL No.None

*For research and further manufacturing use only, not for direct human use.

4',4''',4'''''-nitrilotris(([1,1'-biphenyl]-4-carbaldehyde))|CS-0110964

Structure of 872689-79-7

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General Information

  • CAS No. 872689-79-7
  • Cat. No. CS-0110964
  • Purity ≥97%
  • MDL No. None
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₃₉H₂₇NO₃
  • Molecular Weight 557.64
  • Synonym(s) [1,1'-Biphenyl]-4-carboxaldehyde,4'-[bis(4'-formyl[1,1'-biphenyl]-4-yl)amino]-
  • SMILES O=CC1=CC=C(C2=CC=C(N(C3=CC=C(C4=CC=C(C=O)C=C4)C=C3)C5=CC=C(C6=CC=C(C=O)C=C6)C=C5)C=C2)C=C1

Description

This trisaldehyde features three 4-carbaldehyde groups positioned at the para-positions of biphenyl units, connected through a central nitrilo bridge. The extended π-system enables strong electronic coupling, while the aldehyde functionalities offer high reactivity for conjugation and polymer integration. Designed for precision in molecular architecture, this compound serves as a rigid, multi-functional scaffold in advanced materials synthesis.

Application

4',4''',4'''''-Nitrilotris(([1,1'-biphenyl]-4-carbaldehyde]) serves as a versatile tri-functional building block for the construction of extended π-conjugated systems and multi-chromophoric architectures. Its three aldehyde groups enable efficient condensation reactions, including imine formation and reductive amination, while the biphenyl backbone provides structural rigidity and enhanced electron delocalization. The molecule exhibits good bench stability and facilitates straightforward purification, making it well-suited for applications in organic electronics and molecular scaffold synthesis.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   54.45
  • LogP   9.5949
  • H_Acceptors   4
  • H_Donors   0
  • Rotatable_Bonds   9

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