2,6-Bis(1-methylethoxy)benzoic acid

Base Information

Chemical Name:2,6-Bis(1-methylethoxy)benzoic acid
CAS No.:79128-15-7
Molecular Formula:C13H18O4
Molecular Weight:238.284
Hs Code.:
DSSTox Substance ID:DTXSID001292436
Nikkaji Number:J2.463.890A

Synonyms:SCHEMBL6080226;DTXSID001292436;2,6-Bis(1-methylethoxy)benzoic acid;79128-15-7

Suppliers and Price of 2,6-Bis(1-methylethoxy)benzoic acid

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Chemical Property of 2,6-Bis(1-methylethoxy)benzoic acid

Chemical Property:

XLogP3:2.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:238.12050905
Heavy Atom Count:17
Complexity:232

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)OC1=C(C(=CC=C1)OC(C)C)C(=O)O

Technology Process of 2,6-Bis(1-methylethoxy)benzoic acid

There total 6 articles about 2,6-Bis(1-methylethoxy)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: 98.0%

: 154549-37-8
methyl 2,6-diisopropoxybenzoate

: 79128-15-7
2,6-di(isopropoxy)benzoic acid

Guidance literature:: With potassium hydroxide; In methanol; water; at 80 ℃; for 13h;
DOI:10.1016/S0040-4020(01)80812-7

Reference yield:

: 303-07-1
2,6-Dihydroxybenzoic acid

: 79128-15-7
2,6-di(isopropoxy)benzoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / dimethylformamide / 24 h / Ambient temperature

2: potassium carbonate / dimethylformamide / 48 h / Ambient temperature

3: 98 percent / 20 wtpercent KOH / methanol; H₂O / 13 h / 80 °C

With potassium hydroxide; potassium carbonate; In methanol; water; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(01)80812-7