3,4-Bis(decyloxy)benzoic acid

Base Information

Chemical Name:3,4-Bis(decyloxy)benzoic acid
CAS No.:120878-42-4
Molecular Formula:C27H46O4
Molecular Weight:434.66
Hs Code.:
DSSTox Substance ID:DTXSID70567094
Nikkaji Number:J1.070.916D
Wikidata:Q82452881
Mol file:120878-42-4.mol

Synonyms:3,4-BIS(DECYLOXY)BENZOIC ACID;120878-42-4;SCHEMBL1199875;DTXSID70567094

Suppliers and Price of 3,4-Bis(decyloxy)benzoic acid

Supply Marketing:

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

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Chemical Property of 3,4-Bis(decyloxy)benzoic acid

Chemical Property:

XLogP3:10.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:21
Exact Mass:434.33960994
Heavy Atom Count:31
Complexity:412

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCCCOC1=C(C=C(C=C1)C(=O)O)OCCCCCCCCCC

Technology Process of 3,4-Bis(decyloxy)benzoic acid

There total 11 articles about 3,4-Bis(decyloxy)benzoic acid 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: 96.0%

: 156447-67-5
3,4-di(decyloxy)benzoic acid methyl ester

: 120878-42-4
3,4-di-n-decyloxybenzoic acid

Guidance literature:: With potassium hydroxide; In ethanol; water;
DOI:10.1039/b503591k

Reference yield: 82.0%

: 118468-34-1
3,4-didecyloxybenzaldehyde

: 120878-42-4
3,4-di-n-decyloxybenzoic acid

Guidance literature:: With Jones reagent; In acetone; for 1h;
DOI:10.1021/jo302332u

Reference yield:

: 2150-43-8
3,4-dihydroxybenzoic acid methyl ester

: 120878-42-4
3,4-di-n-decyloxybenzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: K₂CO₃; KI / dimethylformamide / 110 °C

2: aq. KOH / dioxane / 6 h / Heating

With potassium hydroxide; potassium carbonate; potassium iodide; In 1,4-dioxane; N,N-dimethyl-formamide; 1: Williamson etherification;
DOI:10.1021/ja0585477