1,3,5-Trimethoxy-2,4,6-tris[(2-methylphenyl)methyl]benzene

Base Information

Chemical Name:1,3,5-Trimethoxy-2,4,6-tris[(2-methylphenyl)methyl]benzene
CAS No.:845827-23-8
Molecular Formula:C33H36O3
Molecular Weight:480.647
Hs Code.:
DSSTox Substance ID:DTXSID101193869
Nikkaji Number:J2.147.409F

Synonyms:DTXSID101193869;845827-23-8;1,3,5-Trimethoxy-2,4,6-tris[(2-methylphenyl)methyl]benzene

Suppliers and Price of 1,3,5-Trimethoxy-2,4,6-tris[(2-methylphenyl)methyl]benzene

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1,3,5-Trimethoxy-2,4,6-tris[(2-methylphenyl)methyl]benzene

Chemical Property:

XLogP3:8.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:9
Exact Mass:480.26644501
Heavy Atom Count:36
Complexity:533

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=CC=C1CC2=C(C(=C(C(=C2OC)CC3=CC=CC=C3C)OC)CC4=CC=CC=C4C)OC

Technology Process of 1,3,5-Trimethoxy-2,4,6-tris[(2-methylphenyl)methyl]benzene

There total 2 articles about 1,3,5-Trimethoxy-2,4,6-tris[(2-methylphenyl)methyl]benzene 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: 55.0%

: 932-31-0
ortho-tolylmagnesium bromide

: 434323-17-8
1,3,5-tris(bromomethyl)-2,4,6-(trimethoxy)benzene

: 845827-23-8
1,3,5-tris(2'-methylbenzyl)-2,4,6-trimethoxybenzene

Guidance literature:: In toluene; benzene; for 24h; Heating;
DOI:10.1021/ol047597y

Reference yield:

: 621-23-8
1,2,3-trimethoxybenzene

: 845827-23-8
1,3,5-tris(2'-methylbenzyl)-2,4,6-trimethoxybenzene

Guidance literature:: Multi-step reaction with 2 steps

1.1: glacial acetic acid / 1 h

1.2: 37 percent / HBr; AcOH / 3 h / 70 °C

2.1: 55 percent / toluene; benzene / 24 h / Heating

With acetic acid; In toluene; benzene;
DOI:10.1021/ol047597y