2,6-Dimethoxyphenyl benzoate

Base Information

Chemical Name:2,6-Dimethoxyphenyl benzoate
CAS No.:108474-23-3
Molecular Formula:C₁₅H₁₄O₄
Molecular Weight:258.274
Hs Code.:
European Community (EC) Number:682-961-1
NSC Number:113050
DSSTox Substance ID:DTXSID901298455
Nikkaji Number:J3.308.494C
ChEMBL ID:CHEMBL1888934

Synonyms:MLS002706503;2,6-dimethoxyphenyl benzoate;NSC113050;BENZOIC ACID 2,6-DIMETHOXY-PHENYL ESTER;CHEMBL1888934;DTXSID901298455;AKOS024331647;Phenol, 2,6-dimethoxy-, 1-benzoate;Benzoic acid 2,6-dimethoxyphenyl ester;NSC-113050;Benzoic acid, 2,6-dimethoxyphenyl ester;108474-23-3;SMR001573908;benzoic acid (2,6-dimethoxy-phenyl) ester

Suppliers and Price of 2,6-Dimethoxyphenyl benzoate

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 1 raw suppliers

Chemical Property of 2,6-Dimethoxyphenyl benzoate

Chemical Property:

XLogP3:3.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:258.08920892
Heavy Atom Count:19
Complexity:274

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=C(C(=CC=C1)OC)OC(=O)C2=CC=CC=C2

Technology Process of 2,6-Dimethoxyphenyl benzoate

There total 9 articles about 2,6-Dimethoxyphenyl benzoate 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:

: 634-36-6
1,2,3-trimethoxybenzene

: 108474-23-3
2,6-dimethoxyphenyl benzoate

Guidance literature:: Multi-step reaction with 2 steps

1: toluene / Kochen des vom Aether befreiten Reaktionsgemisches

2: pyridine

With pyridine; toluene;
DOI:10.1021/ja01261a023

Reference yield:

: 91-10-1
1,3-dimethoxy-2-hydroxy-benzene

: N′-benzoyl-N,N′-dimethoxybenzohydrazide

: 108474-23-3
2,6-dimethoxyphenyl benzoate

Guidance literature:: With zinc trifluoromethanesulfonate; potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 21h;
DOI:10.1002/adsc.201701646

Reference yield:

: 2446-51-7
N-methoxybenzamide

: 108474-23-3
2,6-dimethoxyphenyl benzoate

Guidance literature:: Multi-step reaction with 2 steps

1: tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 3.5 h / 0 °C / Electrolysis

2: zinc trifluoromethanesulfonate; potassium carbonate / N,N-dimethyl-formamide / 21 h / 20 °C

With tetra-(n-butyl)ammonium iodide; zinc trifluoromethanesulfonate; potassium carbonate; In N,N-dimethyl-formamide;
DOI:10.1002/adsc.201701646