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4,4',4'',4'''-([1,1'-Biphenyl]-4,4'-diylbis(azanetriyl))tetrabenzaldehyde

  • CAS No. 865448-72-2

  • Cat. No. CS-0110885
  • Purity≥97%
  • MDL No.MFCD12031339

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

4,4',4'',4'''-([1,1'-Biphenyl]-4,4'-diylbis(azanetriyl))tetrabenzaldehyde|CS-0110885

Structure of 865448-72-2

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General Information

  • CAS No. 865448-72-2
  • Cat. No. CS-0110885
  • Purity ≥97%
  • MDL No. MFCD12031339
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₄₀H₂₈N₂O₄
  • Molecular Weight 600.66
  • Synonym(s) N,N,N',N'-Tetra(4-formylphenyl)benzidin
  • SMILES O=CC1=CC=C(C=C1)N(C2=CC=C(C=C2)C3=CC=C(C=C3)N(C4=CC=C(C=O)C=C4)C5=CC=C(C=O)C=C5)C6=CC=C(C=O)C=C6

Description

This tetrabenzaldehyde features four aldehyde groups positioned at the 4-positions of a central biphenyl-linked tetraazane scaffold, enabling precise spatial control in multidentate coordination. The extended conjugated framework supports robust π-stacking and facilitates modular integration into supramolecular architectures.

Application

4,4',4'',4'''-([1,1'-Biphenyl]-4,4'-diylbis(azanetriyl))tetrabenzaldehyde serves as a versatile tetradentate ligand scaffold for transition metal coordination, enabling the construction of multidentate complexes with defined geometry. Its four aldehyde functionalities offer high reactivity in imine-based condensations and facilitate conjugation with amine-containing biomolecules or polymers. The biphenyl backbone provides rigidity and π-conjugation, enhancing electronic communication across the ligand framework. This compound demonstrates excellent bench stability and compatibility with standard purification techniques, making it suitable for iterative synthetic workflows in catalysis and materials science.

Safety Information

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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   74.76
  • LogP   9.5432
  • H_Acceptors   6
  • H_Donors   0
  • Rotatable_Bonds   11

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