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Fenazaflor

Base Information
  • Chemical Name:Fenazaflor
  • CAS No.:14255-88-0
  • Molecular Formula:C15H7 Cl2 F3 N2 O2
  • Molecular Weight:375.134
  • Hs Code.:2933990012
  • European Community (EC) Number:238-134-9
  • UNII:4V4BCX2QET
  • DSSTox Substance ID:DTXSID2041969
  • Nikkaji Number:J8.491C
  • Wikidata:Q15632891
  • Mol file:14255-88-0.mol
Fenazaflor

Synonyms:fenazaflor;phenofluorazole

Suppliers and Price of Fenazaflor
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
  • Fenazaflor
  • 1g
  • $ 710.00
  • Sigma-Aldrich
  • Fenazaflor PESTANAL
  • 100mg
  • $ 62.50
Total 16 raw suppliers
Chemical Property of Fenazaflor
Chemical Property:
  • Vapor Pressure:9.59E-08mmHg at 25°C 
  • Melting Point:103℃ 
  • Boiling Point:434.3°Cat760mmHg 
  • Flash Point:216.4°C 
  • PSA:44.12000 
  • Density:1.55g/cm3 
  • LogP:5.40900 
  • Storage Temp.:APPROX 4°C 
  • XLogP3:5.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:2
  • Exact Mass:373.9836673
  • Heavy Atom Count:24
  • Complexity:474
Purity/Quality:

98%Min *data from raw suppliers

Fenazaflor *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:Xn,N 
  • Statements: 21/22-50/53 
  • Safety Statements: 36/37-60-61 
MSDS Files:

SDS file from LookChem

Useful:
  • Chemical Classes:Pesticides -> Other Insecticides
  • Canonical SMILES:C1=CC=C(C=C1)OC(=O)N2C3=CC(=C(C=C3N=C2C(F)(F)F)Cl)Cl
  • Uses Fenazaflor is an acaricide.
Technology Process of Fenazaflor

There total 1 articles about Fenazaflor 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:
Chlorameisensaeurephenylester, 2-Trifluormethyl-5,6-dichlorbenzimidazol;
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