Fenthiaprop

Base Information

Chemical Name:Fenthiaprop
CAS No.:73519-50-3
Deprecated CAS:95721-12-3
Molecular Formula:C16H12 Cl N O4 S
Molecular Weight:349.79
Hs Code.:
UNII:60X8DHC00H
DSSTox Substance ID:DTXSID50914840
Nikkaji Number:J34.358G
Wikidata:Q27155831
Mol file:73519-50-3.mol

Synonyms:Fenthiaprop;73519-50-3;Fenthiaprop [ISO];UNII-60X8DHC00H;60X8DHC00H;HOE 43336;2-[4-[(6-chloro-1,3-benzothiazol-2-yl)oxy]phenoxy]propanoic acid;Propanoic acid, 2-(4-((6-chloro-2-benzothiazolyl)oxy)phenoxy)-;2-[4-(6-chlorobenzo[d]thiazol-2-yl)oxyphenoxy]propanoic acid;95721-12-3;SCHEMBL134264;CHEBI:82242;DTXSID50914840;2-[4-(6-chloro-2-benzthiazolyloxy)-phenoxy]-propionic acid;HOE-43336;C19121;Q27155831;2-{4-[(6-chloro-2-benzothiazolyl)-oxy]-phenoxy}-propionic acid

Suppliers and Price of Fenthiaprop

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 1 raw suppliers

Chemical Property of Fenthiaprop

Chemical Property:

Vapor Pressure:6.11E-12mmHg at 25°C
Melting Point:151 - 152 °C (hexane)
Boiling Point:527.1°C at 760 mmHg
PKA:3.14±0.10(Predicted)
Flash Point:272.6°C
PSA：96.89000
Density:1.452g/cm³
LogP:4.59390
XLogP3:4.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:5
Exact Mass:349.0175567
Heavy Atom Count:23
Complexity:419

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C(=O)O)OC1=CC=C(C=C1)OC2=NC3=C(S2)C=C(C=C3)Cl

Technology Process of Fenthiaprop

There total 3 articles about Fenthiaprop 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: 66.0%

: 66441-10-9
methyl 2-{4-[(6-chloro-2-benzothiazolyl)oxy]phenoxy}propionate

: 73519-50-3,95721-12-3
2-[4-(6-chloro-2-benzthiazolyloxy)-phenoxy]-propionic acid

Guidance literature:: With sodium hydroxide; In tetrahydrofuran;
DOI:10.1021/jm0200097

Reference yield:

: 3622-23-9
2,6-dichloro-1,3-benzothiazole

: 73519-50-3,95721-12-3
2-[4-(6-chloro-2-benzthiazolyloxy)-phenoxy]-propionic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 63 percent / K₂CO₃ / acetonitrile / Heating

2: 66 percent / aq. NaOH / tetrahydrofuran

With sodium hydroxide; potassium carbonate; In tetrahydrofuran; acetonitrile;
DOI:10.1021/jm0200097

Reference yield:

: 60075-04-9
(RS)-methyl 2-(4-hydroxyphenoxy)propionate

: 73519-50-3,95721-12-3
2-[4-(6-chloro-2-benzthiazolyloxy)-phenoxy]-propionic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 63 percent / K₂CO₃ / acetonitrile / Heating

2: 66 percent / aq. NaOH / tetrahydrofuran

With sodium hydroxide; potassium carbonate; In tetrahydrofuran; acetonitrile;
DOI:10.1021/jm0200097