2-(Octyloxy)benzoic acid

Base Information

Chemical Name:2-(Octyloxy)benzoic acid
CAS No.:27830-12-2
Molecular Formula:C15H22O3
Molecular Weight:250.338
Hs Code.:2918990090
European Community (EC) Number:608-139-4
DSSTox Substance ID:DTXSID00602245
Nikkaji Number:J541.567E
Wikidata:Q82499221
Mol file:27830-12-2.mol

Synonyms:2-(OCTYLOXY)BENZOIC ACID;27830-12-2;Benzoic acid, 2-(octyloxy)-;(2-Octyloxy)benzoic Acid;2-n-octyloxybenzoic acid;2-(Octyloxy)benzoicacid;2-octoxybenzoic acid;(octyloxy)benzoic acid;EC 608-139-4;SCHEMBL168816;DTXSID00602245;VSDNNWKISVRDNT-UHFFFAOYSA-N;CBA83012;NS00011475

Suppliers and Price of 2-(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

Crysdot
2-(Octyloxy)benzoicacid 95+%
10g
$ 458.00

American Custom Chemicals Corporation
2-(OCTYLOXY)BENZOIC ACID 95.00%
10G
$ 2638.22

American Custom Chemicals Corporation
2-(OCTYLOXY)BENZOIC ACID 95.00%
5G
$ 2019.23

American Custom Chemicals Corporation
2-(OCTYLOXY)BENZOIC ACID 95.00%
1G
$ 1074.98

Alichem
2-(Octyloxy)benzoicacid
5g
$ 400.00

Total 17 raw suppliers

Chemical Property of 2-(Octyloxy)benzoic acid

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Refractive Index:1.51
Boiling Point:376.923 °C at 760 mmHg
Flash Point:133.565 °C
PSA：46.53000
Density:1.037 g/cm³
LogP:4.12410
XLogP3:5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:9
Exact Mass:250.15689456
Heavy Atom Count:18
Complexity:228

Purity/Quality:

99.9% ^*data from raw suppliers

2-(Octyloxy)benzoicacid 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCOC1=CC=CC=C1C(=O)O

Technology Process of 2-(Octyloxy)benzoic acid

There total 4 articles about 2-(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: 97.0%

: 255062-85-2
2-octyloxybenzoic acid methyl ester

: 27830-12-2
2-octyloxybenzoic acid

Guidance literature:: With sodium hydroxide; In tetrahydrofuran; methanol; water; at 20 - 85 ℃;

Reference yield:

: 111-83-1
1-bromo-octane

: 27830-12-2
2-octyloxybenzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 71 percent / K₂CO₃ / dimethylformamide / 24 h / 90 °C

2: 90 percent / NaOH / methanol / 2 h / Heating

With sodium hydroxide; potassium carbonate; In methanol; N,N-dimethyl-formamide;
DOI:10.1016/j.tet.2007.04.043

Reference yield:

: 119-36-8,8024-54-2
methyl salicylate

: 27830-12-2
2-octyloxybenzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 71 percent / K₂CO₃ / dimethylformamide / 24 h / 90 °C

2: 90 percent / NaOH / methanol / 2 h / Heating

With sodium hydroxide; potassium carbonate; In methanol; N,N-dimethyl-formamide;
DOI:10.1016/j.tet.2007.04.043