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5,5',5'',5'''-(Ethene-1,1,2,2-tetrayl)tetrakis(2-hydroxybenzaldehyde)

  • CAS No. 2036328-15-9

  • Cat. No. CS-0170763
  • Molecule weight508.48
  • Purity≥97%
  • MDL No.MFCD34165654

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

5,5',5'',5'''-(Ethene-1,1,2,2-tetrayl)tetrakis(2-hydroxybenzaldehyde)|CS-0170763

Structure of 2036328-15-9

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General Information

  • CAS No. 2036328-15-9
  • Cat. No. CS-0170763
  • Purity ≥97%
  • MDL No. MFCD34165654
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₃₀H₂₀O₈
  • Molecular Weight 508.48
  • Synonym(s) 2-hydroxy-5-[1,2,2-tris(3-formyl-4-hydroxyphenyl)ethenyl]benzaldehyde
  • SMILES O=CC1=CC(=CC=C1O)C(C2=CC=C(O)C(C=O)=C2)=C(C3=CC=C(O)C(C=O)=C3)C4=CC=C(O)C(C=O)=C4

Description

This tetraaldehyde features four 2-hydroxybenzaldehyde units linked via a central ethene-tetrayl bridge, enabling precise spatial control in coordination chemistry. The ortho-hydroxyl groups facilitate chelation and enhance solubility in polar solvents, while the conjugated framework supports redox activity. Designed for modular ligand synthesis and supramolecular assembly, it delivers structural rigidity and predictable binding geometry under standard conditions.

Application

5,5',5'',5'''-(Ethene-1,1,2,2-tetrayl)tetrakis(2-hydroxybenzaldehyde) serves as a versatile tetradentate ligand precursor, enabling the construction of metal-organic frameworks and coordination complexes through its four phenolic hydroxyl and aldehyde functionalities. Its robust bench stability and orthogonal reactivity profile facilitate straightforward purification and integration into multistep syntheses, particularly in the development of chelating scaffolds for catalytic applications.

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Computational Chemistry Data

  • TPSA   149.2
  • LogP   4.7664
  • H_Acceptors   8
  • H_Donors   4
  • Rotatable_Bonds   8

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