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

Name: 2,4,6-Trichlorobenzene-1,3,5-tricarbaldehyde
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CAS No. 14222-98-1
Cat. No. CS-0110552
Molecule weightNone
Purity≥96%
MDL No.MFCD18429922

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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. MFCD18429922
Storage 4°C, stored under nitrogen
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₉H₃Cl₃O₃
Molecular Weight None
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.

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Signal Word : N/A	UN#: N/A
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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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2,4,6-Trichlorobenzene-1,3,5-tricarbaldehyde

CAS No. 14222-98-1

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