Dimethyl 3,4,5-trimethoxybenzene-1,2-dicarboxylate

Base Information

Chemical Name:Dimethyl 3,4,5-trimethoxybenzene-1,2-dicarboxylate
CAS No.:62267-82-7
Molecular Formula:C₁₃H₁₆O₇
Molecular Weight:284.266
Hs Code.:
DSSTox Substance ID:DTXSID30512040
Nikkaji Number:J2.433.558E
Wikidata:Q82371119

Synonyms:Dimethyl 3,4,5-trimethoxybenzene-1,2-dicarboxylate;62267-82-7;DTXSID30512040

Suppliers and Price of Dimethyl 3,4,5-trimethoxybenzene-1,2-dicarboxylate

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of Dimethyl 3,4,5-trimethoxybenzene-1,2-dicarboxylate

Chemical Property:

XLogP3:1.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:7
Exact Mass:284.08960285
Heavy Atom Count:20
Complexity:344

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of Dimethyl 3,4,5-trimethoxybenzene-1,2-dicarboxylate

There total 4 articles about Dimethyl 3,4,5-trimethoxybenzene-1,2-dicarboxylate 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:

: 186581-53-3,908094-01-9,334-88-3
diazomethane

: 100118-68-1
3,4,5-trimethoxy-phthalic acid-1-methyl ester

: 62267-82-7
dimethyl 3,4,5-trimethoxy-1,2-benzenedicarboxylate

Guidance literature:

Reference yield:

: 1968-71-4
methyl 2-bromo-3,4,5-trimethoxybenzoate

: 62267-82-7
dimethyl 3,4,5-trimethoxy-1,2-benzenedicarboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: magnesium turnings; diethyl ether; iodine / Einleiten von Kohlendioxyd

With diethyl ether; iodine; magnesium;