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Ronoxon

Base Information
  • Chemical Name:Ronoxon
  • CAS No.:3983-45-7
  • Molecular Formula:C8H8 Cl3 O4 P
  • Molecular Weight:305.482
  • Hs Code.:
  • European Community (EC) Number:223-624-7
  • NSC Number:133018
  • UNII:CEW5P2E499
  • DSSTox Substance ID:DTXSID60192894
  • Nikkaji Number:J8.283J
  • Wikidata:Q83065573
  • Mol file:3983-45-7.mol
Ronoxon

Synonyms:O,O-dimethyl O-2,4,5-trichlorophenyl phosphate;ronnel oxygen analog;ronoxon

Suppliers and Price of Ronoxon
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
  • TRC
  • Fenchlorphos-oxon
  • 5mg
  • $ 85.00
  • TRC
  • Fenchlorphos-oxon
  • 250mg
  • $ 965.00
  • Labseeker
  • fenchlorphos-oxon 95
  • 25mg
  • $ 416.00
Total 15 raw suppliers
Chemical Property of Ronoxon
Chemical Property:
  • Vapor Pressure:0.000433mmHg at 25°C 
  • Boiling Point:325.6°Cat760mmHg 
  • Flash Point:207.2°C 
  • PSA:54.57000 
  • Density:1.507g/cm3 
  • LogP:4.42650 
  • Storage Temp.:Hygroscopic, Refrigerator, under inert atmosphere 
  • Solubility.:Chloroform (Slightly), Methanol (Slightly) 
  • XLogP3:3.3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:4
  • Exact Mass:303.922579
  • Heavy Atom Count:16
  • Complexity:270
Purity/Quality:

99% *data from raw suppliers

Fenchlorphos-oxon *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:COP(=O)(OC)OC1=CC(=C(C=C1Cl)Cl)Cl
  • Uses Fenchlorphos-oxon is a pesticide residue found in fruits and vegetables.
Technology Process of Ronoxon

There total 5 articles about Ronoxon 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:
2,4,5-trichlorophenol; With sodium hydride; In tetrahydrofuran; mineral oil; for 0.0833333h;
Dimethyl chlorophosphate; In tetrahydrofuran; mineral oil; at 20 ℃; for 2h;
DOI:10.1021/ja904659e
Guidance literature:
With 3,3-dimethyldioxirane; In dichloromethane; acetone; for 0.0833333h; Yield given; Ambient temperature;
DOI:10.1016/S0040-4039(00)89065-6
Guidance literature:
With methanol; dichloromethane; sodium acetate;
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