Benzaldehyde, 2,2',2''-[1,3,5-benzenetriyltris(methyleneoxy)]tris-

Base Information

• Chemical Name: Benzaldehyde, 2,2',2''-[1,3,5-benzenetriyltris(methyleneoxy)]tris-
• CAS No.: 184587-74-4
• Molecular Formula: C30H24O6
• Molecular Weight: 480.517
• DSSTox Substance ID: DTXSID90451966
• Nikkaji Number: J774.255J
• Wikidata: Q82272291
• Mol file: 184587-74-4.mol

Synonyms:184587-74-4;Benzaldehyde, 2,2',2''-[1,3,5-benzenetriyltris(methyleneoxy)]tris-;DTXSID90451966;1,3,5-tris[(2-formylphenoxy)methyl]benzene;2,2',2''-[1,3,5-Benzenetriyltris(methyleneoxy)]tris[benzaldehyde]

Chemical Property of Benzaldehyde, 2,2',2''-[1,3,5-benzenetriyltris(methyleneoxy)]tris-

Chemical Property:

• XLogP3: 4.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 12
• Exact Mass: 480.15728848
• Heavy Atom Count: 36
• Complexity: 580

Purity/Quality:

99.90% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C(=C1)C=O)OCC2=CC(=CC(=C2)COC3=CC=CC=C3C=O)COC4=CC=CC=C4C=O

Technology Process of Benzaldehyde, 2,2',2''-[1,3,5-benzenetriyltris(methyleneoxy)]tris-

There total 2 articles about Benzaldehyde, 2,2',2''-[1,3,5-benzenetriyltris(methyleneoxy)]tris- 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: 88.0%

1,3,5-Tris(bromomethyl)benzene (18226-42-1) + 2-methyl-benzyl alcohol (89-95-2) → 1,3,5-tri(2'-formylphenyloxamethyl)benzene (184587-74-4)

Guidance literature:

With sodium hydroxide; In ethanol; for 20h; Heating;

DOI:10.1021/jo061616v

Reference yield: 85.0%

1,3,5-Tris(bromomethyl)benzene (18226-42-1) + salicylaldehyde (90-02-8) → 1,3,5-tri(2'-formylphenyloxamethyl)benzene (184587-74-4)

Guidance literature:

With sodium hydroxide; In ethanol; for 3h;

DOI:10.1016/0040-4039(96)01914-4

Reference yield: 88.0%

para-bromoacetophenone (99-90-1) + acetonitrile (75-05-8,26809-02-9) + 1,3,5-tri(2'-formylphenyloxamethyl)benzene (184587-74-4) → C60H54Br3N3O9 (1372112-90-7)

Guidance literature:

With acetyl chloride; at 20 ℃; for 2.25h;

DOI:10.1007/s12039-011-0210-4

upstream raw materials:

1,3,5-Tris(bromomethyl)benzene

salicylaldehyde

2-methyl-benzyl alcohol

Downstream raw materials:

C₆₀H₅₄Br₃N₃O₉