2-naphthyl 3,4,5-trimethoxybenzoate

Base Information

Chemical Name:2-naphthyl 3,4,5-trimethoxybenzoate
CAS No.:457923-26-1
Molecular Formula:C20H18O5
Molecular Weight:338.36
Hs Code.:
Mol file:457923-26-1.mol

Synonyms:2-naphthyl-3',4',5'-trimethoxy benzoate;2-naphthyl,3',4',5'-trimethoxy benzoate;2-naphthyl 3,4,5-trimethoxybenzoate;3,4,5-trimethoxybenzoic acid naphtalen-2-yl ester;

Suppliers and Price of 2-naphthyl 3,4,5-trimethoxybenzoate

Supply Marketing:

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

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Chemical Property of 2-naphthyl 3,4,5-trimethoxybenzoate

Chemical Property:

PSA：53.99000
LogP:4.08480

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 2-naphthyl 3,4,5-trimethoxybenzoate

There total 3 articles about 2-naphthyl 3,4,5-trimethoxybenzoate 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: 84.0%

: 135-19-3
β-naphthol

: 118-41-2
Eudesmic acid

: 457923-26-1
3,4,5-trimethoxybenzoic acid naphthalene-2-yl ester

Guidance literature:: With dmap; dicyclohexyl-carbodiimide; In dichloromethane; for 4h; Heating;
DOI:10.1016/j.bmcl.2006.06.010

Reference yield: 46.0%

: 4521-61-3
3,4,5-Trimethoxybenzoyl chloride

: 135-19-3
β-naphthol

: 457923-26-1
3,4,5-trimethoxybenzoic acid naphthalene-2-yl ester

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃;
DOI:10.1016/S0968-0896(03)00302-X

Reference yield:

: 93-44-7
2-naphthyl benzoate

: 457923-26-1
3,4,5-trimethoxybenzoic acid naphthalene-2-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: human liver microsomal carboxylesterase 1; HEPES buffer / dimethylsulfoxide / pH 7.4

2: 46 percent / triethylamine / CH₂Cl₂ / 20 °C

With HEPES buffer; human liver microsomal carboxylesterase 1; triethylamine; In dichloromethane; dimethyl sulfoxide;
DOI:10.1016/S0968-0896(03)00302-X