Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

Famoxadone

Base Information Edit
  • Chemical Name:Famoxadone
  • CAS No.:131807-57-3
  • Molecular Formula:C22H18N2O4
  • Molecular Weight:374.396
  • Hs Code.:
  • European Community (EC) Number:603-520-1
  • UNII:V1C07OR6II
  • DSSTox Substance ID:DTXSID8034588
  • Nikkaji Number:J974.559I
  • Wikipedia:Famoxadone
  • Wikidata:Q412776
  • ChEMBL ID:CHEMBL1812200
  • Mol file:131807-57-3.mol
Famoxadone

Synonyms:5-methyl-5-(4-phenoxyphenyl)-3-(phenylamino)-2,4-oxazolidinedione;DPX JE874;DPX-JE874;famoxadon;famoxadone;famoxate

Suppliers and Price of Famoxadone
Supply Marketing:Edit
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
  • TRC
  • Famoxadone
  • 10g
  • $ 305.00
  • TRC
  • Famoxadone
  • 1g
  • $ 145.00
  • Sigma-Aldrich
  • Famoxadone solution 100ng/μL in acetonitrile, PESTANAL
  • 2ml-r
  • $ 67.00
  • Medical Isotopes, Inc.
  • Famoxadone
  • 50 g
  • $ 875.00
  • Medical Isotopes, Inc.
  • Famoxadone
  • 1 g
  • $ 620.00
  • ChemScene
  • Famoxadone 98.03%
  • 10mg
  • $ 50.00
  • American Custom Chemicals Corporation
  • FAMOXADONE 98.00%
  • 1G
  • $ 1131.90
  • AHH
  • Famoxadone 98%
  • 1g
  • $ 410.00
Total 58 raw suppliers
Chemical Property of Famoxadone Edit
Chemical Property:
  • Vapor Pressure:8.52E-10mmHg at 25°C 
  • Melting Point:140.3~141.8 °C 
  • Refractive Index:1.659 
  • Boiling Point:491.251 °C at 760 mmHg 
  • PKA:0.63±0.40(Predicted) 
  • Flash Point:250.9 °C 
  • PSA:67.87000 
  • Density:1.328 g/cm3 
  • LogP:4.71090 
  • Storage Temp.:0-6°C 
  • Water Solubility.:0.243 mg-1 (pH 5), 0.011 mg l-1 (pH 7) at 20 °C 
  • XLogP3:5
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:5
  • Exact Mass:374.12665706
  • Heavy Atom Count:28
  • Complexity:563
Purity/Quality:

98% *data from raw suppliers

Famoxadone *data from reagent suppliers

Safty Information:
  • Pictogram(s): HarmfulXn,DangerousN,Flammable
  • Hazard Codes:Xn,N,F 
  • Statements: 48/22-50/53-36-20/21/22-11 
  • Safety Statements: 46-60-61-36-26-16-36/37 
MSDS Files:

SDS file from LookChem

Useful:
  • Chemical Classes:Pesticides -> Fungicides
  • Canonical SMILES:CC1(C(=O)N(C(=O)O1)NC2=CC=CC=C2)C3=CC=C(C=C3)OC4=CC=CC=C4
  • Description Famoxadone is an oxazolidinedione fungicide. Although famoxadone is not a strobilurin derivative, it shares the same mechanism of action. Famoxadone provides control of a broad spectrum of fungi but is particularly effective against downy mildew (P. viticola), late and early blights (Phytophthora infestans and Alternaria solani), the Septoria complex, and barley net blotch at rates of 50 to 200 g ai/ha. Target crops include vines, potatoes/tomatoes, cereals, sugar beets, canola, and cucumber. It shows good protectant, translaminar and residual control, with excellent rainfastness and good crop safety. As was seen for trifloxystrobin, it is particularly effective against grape downy mildew when applied in mixture with cymoxanil. The cereal disease spectrum and level of disease control are improved when famoxadone is mixed with triazole fungicides such as flusilazole.
  • Uses Famoxadone is a known fungicide used in the protection of agricultural products against various fungal diseases and other biotic stresses such as pests. Agricultural fungicide. Famoxadone provides preventive control of a broad spectrum of fungal pathogens such as Plasmopara viticola (grape downy mildew), Phytophthora infestans (potato/ tomato late blight), Pseudoperonospora cubensis (cucumber downy mildew), Septoria tritici (wheat leaf blotch), S. nodorum (wheat glume blotch) and Alternaria solani (potato/tomato early blight).
Technology Process of Famoxadone

There total 6 articles about Famoxadone 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:
Guidance literature:
With acetic acid; phenylhydrazine; In diphenylether; hexane; dichloromethane; water; ethyl acetate;
Guidance literature:
With dmap; acetic acid; In 1,4-dioxane; dichloromethane; water;
Guidance literature:
In dichloromethane; water; acetone;
Post RFQ for Price