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CS-W001157 4
Total: USD 88.00

2,4,6-Trichlorobenzene-1,3,5-tricarbaldehyde

  • CAS No. 14222-98-1

  • Cat. No. CS-0110552
  • Purity≥96%
  • MDL No.None

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

2,4,6-Trichlorobenzene-1,3,5-tricarbaldehyde|CS-0110552

Structure of 14222-98-1

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General Information

  • CAS No. 14222-98-1
  • Cat. No. CS-0110552
  • Purity ≥96%
  • MDL No. None
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₃Cl₃O₃
  • Molecular Weight 265.48
  • Synonym(s) 2,4,6-Trichloro-benzene-1,3,5-tricarbaldehyde
  • SMILES O=CC1=C(C(C=O)=C(C(C=O)=C1Cl)Cl)Cl

Description

2,4,6-Trichlorobenzene-1,3,5-tricarbaldehyde features three electron-deficient aldehyde groups positioned at the 2, 4, and 6 positions of a benzene ring, enabling high reactivity in nucleophilic addition and condensation reactions. The trichloro substitution enhances stability and facilitates selective functionalization under mild conditions. This trialdehyde serves as a rigid, symmetric scaffold for constructing complex molecular architectures in materials science and synthetic organic chemistry.

Application

2,4,6-Trichlorobenzene-1,3,5-tricarbaldehyde serves as a versatile tri-functional building block in synthetic organic chemistry, enabling the construction of complex heterocyclic scaffolds and functionalized aromatic systems. Its three electron-deficient aldehyde groups facilitate efficient condensation reactions, including Mannich and Knoevenagel-type processes, with excellent bench stability and straightforward purification. Functions as a key intermediate in the synthesis of advanced ligands, pharmaceutical precursors, and materials with defined spatial architecture.

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-P330-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   51.21
  • LogP   3.0843
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   3

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