Methyl 4-butoxy-3,5-dimethoxybenzoate

Base Information

Chemical Name:Methyl 4-butoxy-3,5-dimethoxybenzoate
CAS No.:14890-75-6
Molecular Formula:C₁₄H₂₀O₅
Molecular Weight:268.31
Hs Code.:
DSSTox Substance ID:DTXSID201286352

Synonyms:SCHEMBL14999454;ICXWXOZWWKKRCX-UHFFFAOYSA-N;DTXSID201286352;methyl 4-butoxy-3,5-dimethoxybenzoate;methyl 4-n-butoxy-3,5-dimethoxybenzoate;14890-75-6

Suppliers and Price of Methyl 4-butoxy-3,5-dimethoxybenzoate

Supply Marketing:

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

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Chemical Property of Methyl 4-butoxy-3,5-dimethoxybenzoate

Chemical Property:

XLogP3:2.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:8
Exact Mass:268.13107373
Heavy Atom Count:19
Complexity:255

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCOC1=C(C=C(C=C1OC)C(=O)OC)OC

Technology Process of Methyl 4-butoxy-3,5-dimethoxybenzoate

There total 2 articles about Methyl 4-butoxy-3,5-dimethoxybenzoate 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: 94.0%

: 109-65-9
1-bromo-butane

: 884-35-5
methyl syringate

: 14890-75-6
methyl 4-n-butoxy-3,5-dimethoxybenzoate

Guidance literature:: With potassium carbonate; potassium iodide; In N,N-dimethyl-formamide; at 80 ℃; for 24h;

Reference yield:

: 1916-07-0
3,4,5-trimethoxybenzoic acid methyl ester

: 14890-75-6
methyl 4-n-butoxy-3,5-dimethoxybenzoate

Guidance literature:: Multi-step reaction with 2 steps

1: aluminum (III) chloride / dichloromethane / 20 °C

2: potassium carbonate; potassium iodide / N,N-dimethyl-formamide / 24 h / 80 °C

With aluminum (III) chloride; potassium carbonate; potassium iodide; In dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 14890-75-6
methyl 4-n-butoxy-3,5-dimethoxybenzoate

: 363626-73-7
4-butoxy-3,5-dimethoxybenzoic acid chloride

Guidance literature:: Multi-step reaction with 2 steps

1: KOH / methanol / 65 °C

2: SOCl₂ / toluene / 110 °C

With potassium hydroxide; thionyl chloride; In methanol; toluene;
DOI:10.1021/jm0011272