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Kresoxim-Methyl

Base Information Edit
  • Chemical Name:Kresoxim-Methyl
  • CAS No.:143390-89-0
  • Molecular Formula:C18H19NO4
  • Molecular Weight:313.353
  • Hs Code.:29252900
  • European Community (EC) Number:417-880-0,604-351-6
  • UNII:0LXZ062TTB
  • DSSTox Substance ID:DTXSID2032558
  • Nikkaji Number:J1.157.567F,J1.641.072A,J588.356C
  • Metabolomics Workbench ID:70709
  • ChEMBL ID:CHEMBL203191
  • Mol file:143390-89-0.mol
Kresoxim-Methyl

Synonyms:BAS 490 F;BAS 490F;BAS-490 F;BAS-490-02F;BAS-490F;kresoxim methyl ester;kresoxim-methyl;methyl (E)-methoxyimino(alpha-(o-tolyloxy)-o-tolyl)acetate;methyl 2- methoxyimino-2-(2-(o-tolyloxymethyl)phenyl)acetate

Suppliers and Price of Kresoxim-Methyl
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
  • Usbiological
  • Kresoxim-methyl
  • 100mg
  • $ 418.00
  • TRC
  • Kresoxim-methyl
  • 1g
  • $ 185.00
  • Sigma-Aldrich
  • Kresoxim-methyl PESTANAL
  • 100mg
  • $ 138.00
  • Crysdot
  • (E)-Methyl2-(methoxyimino)-2-(2-((o-tolyloxy)methyl)phenyl)acetate 97%
  • 25g
  • $ 59.00
  • Cayman Chemical
  • Kresoxim-methyl ≥95%
  • 100mg
  • $ 105.00
  • Cayman Chemical
  • Kresoxim-methyl ≥95%
  • 50mg
  • $ 63.00
  • Cayman Chemical
  • Kresoxim-methyl ≥95%
  • 25mg
  • $ 35.00
  • AK Scientific
  • Kresoxim-methyl
  • 5g
  • $ 990.00
Total 100 raw suppliers
Chemical Property of Kresoxim-Methyl Edit
Chemical Property:
  • Vapor Pressure:1.4E-07mmHg at 25°C 
  • Melting Point:98-100 °C 
  • Refractive Index:1.53 
  • Boiling Point:429.4 °C at 760 mmHg 
  • Flash Point:171.2 °C 
  • PSA:57.12000 
  • Density:1.1 g/cm3 
  • LogP:3.09750 
  • Storage Temp.:0-6°C 
  • Water Solubility.:2 mg l-1(20 °C) 
  • XLogP3:4.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:7
  • Exact Mass:313.13140809
  • Heavy Atom Count:23
  • Complexity:410
Purity/Quality:

99% *data from raw suppliers

Kresoxim-methyl *data from reagent suppliers

Safty Information:
  • Pictogram(s): HarmfulXn,Dangerous
  • Hazard Codes:Xn;N,N,Xn 
  • Statements: 40-50/53 
  • Safety Statements: 2-36/37-60-61 
MSDS Files:

SDS file from LookChem

Useful:
  • Chemical Classes:Pesticides -> Fungicides
  • Canonical SMILES:CC1=CC=CC=C1OCC2=CC=CC=C2C(=NOC)C(=O)OC
  • Isomeric SMILES:CC1=CC=CC=C1OCC2=CC=CC=C2/C(=N\OC)/C(=O)OC
  • Uses It is a kind of Strobilurin fungicide and is mainly applied to cereals, rice, potatoes, apples, pears, pumpkins and grapes. It also has protection, treatment and eradication activity on the Ascomycetes, Basidiomycetes, Deuteromycetes and Oomycetes and other pathogenic fungi with long duration period. Under recommended dose, it is safe to crops without injury-free and safe for the environment. Agricultural fungicide. An agricultural fungicide. Kresoxim-methyl is used for the control of several diseases (scab, mildews, blast, sheath blight and others) on a range of crops including apples, pears, vines, sugar beet and cereals.
  • Description Kresoxim-methyl is a strobilurin fungicide. It inhibits conidial germination of V. inaequalis isolates from apple orchards (EC50s = 0.00033-0.0078 mg/L). Kresoxim-methyl also inhibits mycelial growth (EC50 = 0.240 mg/L) and is fungicidal against Saprolegnia (MIC = 1 mg/L). It increases intracellular calcium levels and disrupts the mitochondrial membrane potential in mouse cortical cultures in a concentration-dependent manner. Kresoxim-methyl is toxic to goldfish (C. auratus; LC50 = 0.807 mg/L).
Technology Process of Kresoxim-Methyl

There total 22 articles about Kresoxim-Methyl 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 copper(l) iodide; In butanone; for 4h; Concentration; Reagent/catalyst; Reflux;
Refernces Edit
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