5-(3-Carboxybenzoyl)-2-((6-(4-methoxyphenyl)-5-hexenyl)oxy)benzenepropanoic acid

Base Information

Chemical Name:5-(3-Carboxybenzoyl)-2-((6-(4-methoxyphenyl)-5-hexenyl)oxy)benzenepropanoic acid
CAS No.:117423-74-2
Molecular Formula:C30H30 O7
Molecular Weight:502.564
Hs Code.:
UNII:XG52JC545T
Nikkaji Number:J350.714I
Pharos Ligand ID:Y5WV39A95G7D
ChEMBL ID:CHEMBL49302
Mol file:117423-74-2.mol

Synonyms:5-(3-carboxybenzoyl)-2-((6-(4-methoxyphenyl)-5-hexenyl)oxy)benzenepropanoic acid;CGS 23131;LY 223982;LY 233978 disodium salt;LY-223982;SK and F 107324;SK and F-107324;SKF 107324

Suppliers and Price of 5-(3-Carboxybenzoyl)-2-((6-(4-methoxyphenyl)-5-hexenyl)oxy)benzenepropanoic 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 4 raw suppliers

Chemical Property of 5-(3-Carboxybenzoyl)-2-((6-(4-methoxyphenyl)-5-hexenyl)oxy)benzenepropanoic acid

Chemical Property:

Vapor Pressure:7.11E-24mmHg at 25°C
Boiling Point:753.8°Cat760mmHg
Flash Point:248.4°C
Density:1.235g/cm³
XLogP3:5.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:14
Exact Mass:502.19915329
Heavy Atom Count:37
Complexity:755

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=C(C=C1)C=CCCCCOC2=C(C=C(C=C2)C(=O)C3=CC(=CC=C3)C(=O)O)CCC(=O)O
Isomeric SMILES:COC1=CC=C(C=C1)/C=C/CCCCOC2=C(C=C(C=C2)C(=O)C3=CC(=CC=C3)C(=O)O)CCC(=O)O

Technology Process of 5-(3-Carboxybenzoyl)-2-((6-(4-methoxyphenyl)-5-hexenyl)oxy)benzenepropanoic acid

There total 12 articles about 5-(3-Carboxybenzoyl)-2-((6-(4-methoxyphenyl)-5-hexenyl)oxy)benzenepropanoic 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: 64.0%

: 128577-80-0
3-{3-(2-Ethoxycarbonyl-ethyl)-4-[(E)-6-(4-methoxy-phenyl)-hex-5-enyloxy]-benzoyl}-benzoic acid ethyl ester

: 117423-74-2
LY223982

Guidance literature:: With potassium hydroxide; In ethanol; at 25 ℃; for 1h;
DOI:10.1021/jm00172a020

Reference yield: 64.0%

: 117423-74-2
LY223982

Guidance literature:

Reference yield:

: 128577-60-6
(5E)-6-(4-Methoxyphenyl)-5-hexen-1-ol

: 117423-74-2
LY223982

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine (TEA) / diethyl ether

2: 1.) 60percent sodium hydride disp. in oil / 1.) DMF, 25 deg C, 30 min, 2.) 65 deg C

3: 64 percent / KOH / aq. ethanol / 1 h / 25 °C

With potassium hydroxide; sodium hydride; triethylamine; In diethyl ether; ethanol;
DOI:10.1021/jm00172a020