Fluazifop, ethyl ester

Base Information

Chemical Name:Fluazifop, ethyl ester
CAS No.:69045-80-3
Molecular Formula:C17H16F3NO4
Molecular Weight:355.314
Hs Code.:
DSSTox Substance ID:DTXSID801161059

Synonyms:Fluazifop, ethyl ester;69045-80-3;Fluazifop-ethyl;SCHEMBL10873975;DTXSID801161059;Ethyl 2-[4-[[5-(trifluoromethyl)-2-pyridyl]oxy]phenoxy]propanoate;Ethyl 2-[4-[[5-(trifluoromethyl)-2-pyridinyl]oxy]phenoxy]propanoate

Suppliers and Price of Fluazifop, ethyl ester

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

Usbiological
Fluazifop-ethyl
50mg
$ 460.00

TRC
Fluazifop-ethyl
50mg
$ 165.00

Total 0 raw suppliers

Chemical Property of Fluazifop, ethyl ester

Chemical Property:

Boiling Point:182 - 185 °C (3 mmHg)
PSA：57.65000
LogP:4.22310
XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:7
Exact Mass:355.10314248
Heavy Atom Count:25
Complexity:425

Purity/Quality:: Fluazifop-ethyl ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C(C)OC1=CC=C(C=C1)OC2=NC=C(C=C2)C(F)(F)F
Uses Fluazifop-ethyl is an intermediate in the synthesis of (±)-Fluazifop (F407430). (±)-Fluazifop is a grass-selective herbicide which inhibits acetyl-CoA carboxylase in sensitive plant species.

Technology Process of Fluazifop, ethyl ester

There total 2 articles about Fluazifop, ethyl ester 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: 83.0%

: 69045-85-8
2-(4-hydroxyphenoxy)-5-trifluoromethylpyridine

: 535-11-5,41978-69-2
Ethyl 2-bromopropionate

: 69045-80-3
ethyl 2-[4-[[5-(trifluoromethyl)-2-pyridyl]oxy]phenoxy]propanoate

Guidance literature:: With potassium carbonate; In acetonitrile; at 70 ℃; for 16h;

Reference yield:

: 69045-80-3
ethyl 2-[4-[[5-(trifluoromethyl)-2-pyridyl]oxy]phenoxy]propanoate

Guidance literature:: Carbonsaeure, 1) SOCl2, 2) Ethanol/Triethylamin;

Reference yield:

: 69045-80-3
ethyl 2-[4-[[5-(trifluoromethyl)-2-pyridyl]oxy]phenoxy]propanoate

: 1456712-14-3
(1E)-2-[4-[[5-(trifluoromethyl)-2-pyridyl]oxy]phenoxy]propanal oxime

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium aluminium tetrahydride / tetrahydrofuran / 20 °C / Cooling with ice

1.2: 0 °C

2.1: Dess-Martin periodane / dichloromethane / 2.25 h / 20 °C

3.1: hydroxylamine hydrochloride; sodium carbonate / ethanol / 70 °C

With lithium aluminium tetrahydride; hydroxylamine hydrochloride; sodium carbonate; Dess-Martin periodane; In tetrahydrofuran; ethanol; dichloromethane;