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Flumequine

Base Information Edit
  • Chemical Name:Flumequine
  • CAS No.:42835-25-6
  • Deprecated CAS:143984-63-8
  • Molecular Formula:C14H12FNO3
  • Molecular Weight:261.253
  • Hs Code.:2933990090
  • European Community (EC) Number:255-962-6
  • NSC Number:757806
  • UNII:UVG8VSP2SJ
  • DSSTox Substance ID:DTXSID5045623
  • Nikkaji Number:J16.025C
  • Wikipedia:Flumequine
  • Wikidata:Q3074500
  • NCI Thesaurus Code:C80639
  • Metabolomics Workbench ID:49610
  • ChEMBL ID:CHEMBL370252
  • Mol file:42835-25-6.mol
Flumequine

Synonyms:Apurone;flumequine;R 802;R-802

Suppliers and Price of Flumequine
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
  • Flumequine
  • 500ul
  • $ 360.00
  • Usbiological
  • Flumequine
  • 500ul
  • $ 306.00
  • TRC
  • Flumequine
  • 10mg
  • $ 50.00
  • TRC
  • Flumequine
  • 50mg
  • $ 60.00
  • TCI Chemical
  • Flumequine >98.0%(HPLC)(T)
  • 25g
  • $ 246.00
  • TCI Chemical
  • Flumequine >98.0%(HPLC)(T)
  • 5g
  • $ 91.00
  • Sigma-Aldrich
  • Flumequine
  • 1g
  • $ 46.30
  • Sigma-Aldrich
  • Flumequine VETRANAL
  • 250mg
  • $ 55.90
  • Sigma-Aldrich
  • Flumequine
  • 5g
  • $ 144.00
  • Sigma-Aldrich
  • Flumequine European Pharmacopoeia (EP) Reference Standard
  • $ 190.00
Total 154 raw suppliers
Chemical Property of Flumequine Edit
Chemical Property:
  • Appearance/Colour:white to off-white powder 
  • Vapor Pressure:1.66E-08mmHg at 25°C 
  • Melting Point:253- 255 °C 
  • Refractive Index:1.645 
  • Boiling Point:439.7 °C at 760 mmHg 
  • PKA:pKa 6.42(H2O t=25.0 I=0.025)(Approximate) 
  • Flash Point:219.7 °C 
  • PSA:59.30000 
  • Density:1.45 g/cm3 
  • LogP:2.34600 
  • Storage Temp.:0-6°C 
  • Solubility.:1 M NH4OH: soluble50mg/mL 
  • Water Solubility.:Soluble in DMSO and dilute alkali hydroxides. Insoluble in water 
  • XLogP3:2.9
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:1
  • Exact Mass:261.08012141
  • Heavy Atom Count:19
  • Complexity:462
Purity/Quality:

99% *data from raw suppliers

Flumequine *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 22-24/25-36/37/39-27-26 
MSDS Files:

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CC1CCC2=C3N1C=C(C(=O)C3=CC(=C2)F)C(=O)O
  • Description Flumequine is a synthetic antibiotic belonging to the second-generation quinolone group and is mainly active against Gram negative bacteria. It is currently the only non-humans shared broad-spectrum antimicrobial veterinary drug. It is taken as the substitute product of norfloxacin. It has a strong bactericidal activity with excellent efficacy in the treatment of animal bacterial diseases. Its main effect is to inhibit bacterial deoxy nucleic acid (DNA) gyrase, interfering with the deoxyribonucleic acid (DNA) synthesis, thereby causing failure of cell for further division, and thus playing the role of killing bacteria. It is used in bovine, ovine, chicken, rabbits, goats, horses and salmonidae, however the establishment of MRLs was only requested for non-lactating cattle, pigs, sheep, chicken and salmonidae.
  • Uses Flumequine is a fluoroquinolone compound with antimicrobial activity against Gram-negative organisms. It is used in the treatment of enteric infections in food animals and in the treatment of bacterial infections in farmed fish. Flumequine is replacing oxolinic acid in aquaculture because of its more appropriate pharmacokinetic profile and lower effective doses (Treves-Brown 2000). Flumequine also has limited use in humans for the treatment of urinary tract infections.
  • Therapeutic Function Antibacterial
Technology Process of Flumequine

There total 8 articles about Flumequine 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 sodium hydroxide; PPA; In 5,5-dimethyl-1,3-cyclohexadiene;
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