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

Base Information

• Chemical Name: 2,4,6-Trichlorobenzene-1,3,5-tricarbaldehyde
• CAS No.: 14222-98-1
• Molecular Formula: C₉H₃Cl₃O₃
• Molecular Weight: 265.48

Synonyms:2,4,6-trichlorobenzene-1,3,5-tricarbaldehyde;14222-98-1;2,4,6-Trichloro-benzene-1,3,5-tricarbaldehyde;2,4,6-Trichlor-1,3,5-trialdehyde-benzene;YSZC222;SCHEMBL21643711;AMY25175;BS-45849;CS-0110552;2,4,6-trichloro-1,3,5-benzenetricarbaldehyde;E81333

Chemical Property of 2,4,6-Trichlorobenzene-1,3,5-tricarbaldehyde

Chemical Property:

• PSA: 51.21000
• LogP: 3.08430
• XLogP3: 2.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 263.914777
• Heavy Atom Count: 15
• Complexity: 211

Purity/Quality:

99%, ^*data from raw suppliers

2,4,6-Trichlorobenzene-1,3,5-tricarbaldehyde 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C(=O)C1=C(C(=C(C(=C1Cl)C=O)Cl)C=O)Cl

Technology Process of 2,4,6-Trichlorobenzene-1,3,5-tricarbaldehyde

There total 6 articles about 2,4,6-Trichlorobenzene-1,3,5-tricarbaldehyde which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 91.0%

α,α,α',α',α'',α'',2,4,6-nonachloromesitylene (40860-87-5) → 2,4,6-trichlorobenzene-1,3,5-tricarbaldehyde (14222-98-1)

Guidance literature:

With sulfuric acid; iron(II) sulfate; at 125 ℃; for 5h;

DOI:10.1021/ol901127q

Reference yield:

1,3,5-trichloro-2,4,6-trimethylbenzene (5324-68-5) → 2,4,6-trichlorobenzene-1,3,5-tricarbaldehyde (14222-98-1)

Guidance literature:

Multi-step reaction with 2 steps

1: Cl₂ / CCl₄ / 12 h / Heating; Irradiation

2: FeSO₄, H₂SO₄ / 125 °C

With sulfuric acid; chlorine; iron(II) sulfate; In tetrachloromethane;

DOI:10.1016/S0040-4020(01)82585-0

Reference yield:

1,3,5-trimethyl-benzene (108-67-8) → 2,4,6-trichlorobenzene-1,3,5-tricarbaldehyde (14222-98-1)

Guidance literature:

Multi-step reaction with 3 steps

1: Cl₂ / CCl₄ / 12 h / 15 - 20 °C

2: Cl₂ / CCl₄ / 12 h / Heating; Irradiation

3: FeSO₄, H₂SO₄ / 125 °C

With sulfuric acid; chlorine; iron(II) sulfate; In tetrachloromethane;

DOI:10.1016/S0040-4020(01)82585-0

upstream raw materials:

α,α,α',α',α'',α'',2,4,6-nonachloromesitylene

1,3,5-trichloro-2,4,6-trimethylbenzene

1,3,5-trimethyl-benzene

α,α',α'',2,4,6-Hexachlor-mesitylen

Downstream raw materials:

benzo[1,2-b:3,4-b':5,6-b]trithiophene-2,5,8 tricarbaldehyde

2.4.6-Trichlor-benzoltrialdehyd-(1.3.5)-trioxim

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