2,4,6-Trimethylphenyl 2-methoxybenzoate

Base Information

Chemical Name:2,4,6-Trimethylphenyl 2-methoxybenzoate
CAS No.:77408-43-6
Molecular Formula:C17H18O3
Molecular Weight:270.328
Hs Code.:
DSSTox Substance ID:DTXSID70506509
Wikidata:Q82362279

Synonyms:77408-43-6;2,4,6-Trimethylphenyl 2-methoxybenzoate;DTXSID70506509

Suppliers and Price of 2,4,6-Trimethylphenyl 2-methoxybenzoate

Supply Marketing:

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

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Chemical Property of 2,4,6-Trimethylphenyl 2-methoxybenzoate

Chemical Property:

XLogP3:4.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:270.125594432
Heavy Atom Count:20
Complexity:316

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=C(C(=C1)C)OC(=O)C2=CC=CC=C2OC)C

Technology Process of 2,4,6-Trimethylphenyl 2-methoxybenzoate

There total 3 articles about 2,4,6-Trimethylphenyl 2-methoxybenzoate 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: 49.0%

: 51114-00-2
sodium 2,4,6-trimethylphenoxide

: 21615-34-9
2-Methoxybenzoyl chloride

: 77408-43-6
2,4,6-trimethylphenyl 2-methoxybenzoate

Guidance literature:: In toluene; for 2h; Heating;

Reference yield:

: 579-75-9
2-Methoxybenzoic acid

: 77408-43-6
2,4,6-trimethylphenyl 2-methoxybenzoate

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / 3 h / Heating

2: 4-dimethylaminopyridine, pyridine / benzene / 4 h / Ambient temperature

With pyridine; dmap; thionyl chloride; In benzene;
DOI:10.1246/bcsj.66.3034