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1-Fluoro-3-nitrobenzene

Base Information Edit
  • Chemical Name:1-Fluoro-3-nitrobenzene
  • CAS No.:402-67-5
  • Molecular Formula:C6H4FNO2
  • Molecular Weight:141.102
  • Hs Code.:2904.90
  • European Community (EC) Number:206-953-0
  • NSC Number:60651
  • UNII:CCK4NSJ7M3
  • DSSTox Substance ID:DTXSID20193201
  • Nikkaji Number:J47.808C
  • Wikidata:Q63395619
  • ChEMBL ID:CHEMBL164634
  • Mol file:402-67-5.mol
1-Fluoro-3-nitrobenzene

Synonyms:1-FLUORO-3-NITROBENZENE;402-67-5;3-Fluoronitrobenzene;m-Fluoronitrobenzene;Benzene, 1-fluoro-3-nitro-;m-Nitrofluorobenzene;CCK4NSJ7M3;EINECS 206-953-0;NSC 60651;NSC-60651;3-fluoro-1-nitrobenzene;1-fluoro-3-nitro benzene;1-Fluoro-3-nitro-benzene;NSC60651;3-nitrofluorobenzene;MFCD00007196;3-fluoro-nitrobenzene;3-nitro-fluorobenzene;3-fluoro nitro benzene;2-fluoro-4-nitrobenzene;UNII-CCK4NSJ7M3;SCHEMBL248013;META FLUORO NITROBENZENE;CHEMBL164634;1-NITRO-3-FLUOROBENZENE;1-Fluoro-3-nitrobenzene, 97%;DTXSID20193201;BCP16131;AKOS000120876;AKOS040744780;AC-2900;CS-W018306;AS-33375;AM20040406;F0110;FT-0615737;EN300-20820;A25214;1-Fluoro-3-nitrobenzene, purum, >=97.0% (GC);W-106366;N-Methyl-N-[(4-methyl-1,3-thiazol-5-yl)methyl]amin;Q63395619;3-FluoronitrobenzenE;3-Fluoro-1-nitrobenzene;M-Nitrofluorobenzene

Suppliers and Price of 1-Fluoro-3-nitrobenzene
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
  • TRC
  • 3-Fluoronitrobenzene
  • 5g
  • $ 85.00
  • TRC
  • 3-Fluoronitrobenzene
  • 250g
  • $ 330.00
  • TCI Chemical
  • 3-Fluoronitrobenzene >97.0%(GC)
  • 25g
  • $ 53.00
  • SynQuest Laboratories
  • 3-Fluoronitrobenzene 97%
  • 25 g
  • $ 24.00
  • SynQuest Laboratories
  • 3-Fluoronitrobenzene 97%
  • 100 g
  • $ 72.00
  • Sigma-Aldrich
  • 1-Fluoro-3-nitrobenzene 97%
  • 10g
  • $ 29.80
  • Oakwood
  • 1-Fluoro-3-nitrobenzene 99%
  • 25g
  • $ 15.00
  • Oakwood
  • 1-Fluoro-3-nitrobenzene 99%
  • 5g
  • $ 10.00
  • Oakwood
  • 1-Fluoro-3-nitrobenzene 99%
  • 1g
  • $ 9.00
  • Oakwood
  • 1-Fluoro-3-nitrobenzene 99%
  • 100g
  • $ 40.00
Total 110 raw suppliers
Chemical Property of 1-Fluoro-3-nitrobenzene Edit
Chemical Property:
  • Appearance/Colour:clear brown liquid 
  • Melting Point:1.7 °C(lit.) 
  • Refractive Index:1.525 
  • Boiling Point:199.8 °C at 760 mmHg 
  • Flash Point:76.7 °C 
  • PSA:45.82000 
  • Density:1.337 g/cm3 
  • LogP:2.25710 
  • Storage Temp.:Store below +30°C. 
  • Water Solubility.:immiscible 
  • XLogP3:1.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:0
  • Exact Mass:141.02260653
  • Heavy Atom Count:10
  • Complexity:134
Purity/Quality:

99% *data from raw suppliers

3-Fluoronitrobenzene *data from reagent suppliers

Safty Information:
  • Pictogram(s): HarmfulXn, ToxicT, IrritantXi 
  • Hazard Codes:T,Xi,Xn 
  • Statements: 23/24/25-33-20/21/22 
  • Safety Statements: 36/37-45-36 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC(=CC(=C1)F)[N+](=O)[O-]
  • Uses 1-Fluoro-3-nitrobenzene is a di-substitiuted benzene derivative used for the synthesis of fluoroaromatic compounds through fluorodenitration and other pharmaceuticals. 1-Fluoro-3-nitrobenzene was used as an internal standard in the regiospecific silver-mediated fluorination of aryl silanes.
Technology Process of 1-Fluoro-3-nitrobenzene

There total 70 articles about 1-Fluoro-3-nitrobenzene 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:
3-nitro-aniline; With tetrafluoroboric acid; 1-ethyl-3-methylimidazolium tetrafluoroborate; sodium nitrite; at 0 - 20 ℃; for 12.5h;
at 50 ℃;
DOI:10.1016/S0022-1139(00)00337-7
Guidance literature:
With potassium fluoride; phthaloyl fluoride; tetramethlyammonium chloride; In sulfolane; at 160 ℃; for 8h;
DOI:10.1021/jo00022a037
Guidance literature:
With boron trifluoride diethyl etherate; at 120 - 125 ℃; for 1h;
DOI:10.1080/00397919308011253
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