3,5-Bis(octyloxy)benzoic acid

Base Information

Chemical Name:3,5-Bis(octyloxy)benzoic acid
CAS No.:87963-85-7
Molecular Formula:C23H38O4
Molecular Weight:378.552
Hs Code.:
DSSTox Substance ID:DTXSID10607226
Nikkaji Number:J1.906.785H
Wikidata:Q82506197

Synonyms:3,5-BIS(OCTYLOXY)BENZOIC ACID;87963-85-7;3,5-dioctoxybenzoic acid;3,5-Dioctyloxybenzoic acid;Benzoic acid, 3,5-bis(octyloxy)-;SCHEMBL11050536;DTXSID10607226;CS-0457748;A1-05336

Suppliers and Price of 3,5-Bis(octyloxy)benzoic acid

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
Packaging
price

Total 2 raw suppliers

Chemical Property of 3,5-Bis(octyloxy)benzoic acid

Chemical Property:

XLogP3:8.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:17
Exact Mass:378.27700969
Heavy Atom Count:27
Complexity:332

Purity/Quality:: 99.0% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCCCCCOC1=CC(=CC(=C1)C(=O)O)OCCCCCCCC

Technology Process of 3,5-Bis(octyloxy)benzoic acid

There total 7 articles about 3,5-Bis(octyloxy)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: 100.0%

: 87963-84-6
methyl 3,5-bis(octyloxy)benzoate

: 87963-85-7
3,5-bis(octyloxy)benzoic acid

Guidance literature:: With potassium hydroxide; In ethanol; at 100 ℃; for 2h;
DOI:10.1021/acs.biomac.8b01405

Reference yield:

: 2150-44-9
1-carbomethoxy-3,5-dihydroxybenzene

: 87963-85-7
3,5-bis(octyloxy)benzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / K₂CO₃; Adogen 464 / acetone / Heating

2: 86 percent / NaOH / methanol / Heating

With sodium hydroxide; adogen 464; potassium carbonate; In methanol; acetone;
DOI:10.1039/b615545f

Reference yield:

: 111-83-1
1-bromo-octane

: 87963-85-7
3,5-bis(octyloxy)benzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / K₂CO₃ / acetonitrile / 100 °C

2: 98 percent / KOH / ethanol / 4 h / Heating

With potassium hydroxide; potassium carbonate; In ethanol; acetonitrile;
DOI:10.1055/s-2004-831241