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FUBERIDAZOLE

Base Information
  • Chemical Name:FUBERIDAZOLE
  • CAS No.:3878-19-1
  • Deprecated CAS:1135441-28-9
  • Molecular Formula:C11H8N2O
  • Molecular Weight:184.197
  • Hs Code.:2934999090
  • European Community (EC) Number:223-404-0
  • NSC Number:72670
  • UN Number:2811,2902
  • UNII:RXD450F6C7
  • DSSTox Substance ID:DTXSID4041995
  • Nikkaji Number:J2.201B
  • Wikipedia:Fuberidazole
  • Wikidata:Q5506905
  • Metabolomics Workbench ID:87104
  • ChEMBL ID:CHEMBL201094
  • Mol file:3878-19-1.mol
FUBERIDAZOLE

Synonyms:Fubridazole;2-(2-Furanyl)-1H-benzimidazole;2-(furan-2-yl)-benzimidazole;2-(furan-2-yl)-1H-benzo[d]imidazole;Benzimidazole,2-(2-furyl);2-(furan-2-yl)-1H-benzimidazole;Fuberidatol;2-(2'-furyl)-benzimidazole;Voronite;Fuberidazol;Furidazole;Furidazol;2-(2-furyl)benzimidazole;Fuberisazol;2-(furan-2-yl)-1H-1,3-benzimidazole;2-(2'-furyl)-1H-benzimidazole;Voronit;

Suppliers and Price of FUBERIDAZOLE
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
  • Fuberidazole
  • 50mg
  • $ 150.00
  • TRC
  • Fuberidazole
  • 10mg
  • $ 60.00
  • TRC
  • Fuberidazole
  • 5mg
  • $ 45.00
  • Sigma-Aldrich
  • Fuberidazole PESTANAL
  • 250mg
  • $ 86.10
  • Oakwood
  • 2-Furan-2-yl-1H-benzoimidazole 97%
  • 1g
  • $ 44.00
  • Matrix Scientific
  • 2-(2-Furyl)-1H-benzimidazole
  • 500mg
  • $ 126.00
  • Matrix Scientific
  • 2-(2-Furyl)-1H-benzimidazole
  • 1g
  • $ 158.00
  • Matrix Scientific
  • 2-(2-Furyl)-1H-benzimidazole
  • 5g
  • $ 483.00
  • Crysdot
  • 2-(Furan-2-yl)-1H-benzo[d]imidazole 95+%
  • 25g
  • $ 529.00
  • Chemenu
  • 2-(2-Furyl)-1H-benzimidazole 95%
  • 5g
  • $ 266.00
Total 22 raw suppliers
Chemical Property of FUBERIDAZOLE
Chemical Property:
  • Vapor Pressure:5.37E-06mmHg at 25°C 
  • Melting Point:310-312℃ 
  • Refractive Index:1.5300 (estimate) 
  • Boiling Point:380.6°C at 760 mmHg 
  • PKA:4.6 (base) 
  • Flash Point:194.7°C 
  • PSA:41.82000 
  • Density:1.286g/cm3 
  • LogP:2.82290 
  • Storage Temp.:0-6°C 
  • Solubility.:DMSO (Slightly), Methanol (Slightly) 
  • Water Solubility.:200 mg l-1 (pH 4), 71 mg l-1 (pH 7) at 20 °C 
  • XLogP3:2.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:1
  • Exact Mass:184.063662883
  • Heavy Atom Count:14
  • Complexity:210
  • Transport DOT Label:Poison
Purity/Quality:

98% *data from raw suppliers

Fuberidazole *data from reagent suppliers

Safty Information:
  • Pictogram(s): Xn,N,T 
  • Hazard Codes:Xn,N,T 
  • Statements: 22-50/53-23-21-48/22-43-40-21/22 
  • Safety Statements: 22-60-61-45-36/37 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)NC(=N2)C3=CC=CO3
  • Uses Fuberidazole is a systemic fungicide used in cereal seed dressing to control a variety of soil and seed borne diseases caused by Fusarium spp. It is also used as an anthelmintic and an inhibitor of enteroviruses. Fuberidazole is a benzimidazole based fungicide used as a fungicidal seed treatment of barley.
Technology Process of FUBERIDAZOLE

There total 69 articles about FUBERIDAZOLE 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 hydrogen; In ethyl acetate; at 70 ℃; for 20h; under 7500.75 Torr; Autoclave; Green chemistry;
DOI:10.1002/cssc.202002344
Guidance literature:
With hydrogen; In ethyl acetate; at 60 ℃; for 20h; under 7500.75 Torr; Autoclave; Green chemistry;
DOI:10.1002/cssc.202002344
Guidance literature:
With Al cations incorporated into the Si framework; open air; In neat (no solvent); at 100 ℃; for 15h; Green chemistry;
DOI:10.1039/d1gc02627e
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