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4-Nitro-2-(4-nitropyridin-2-yl)-1-oxidopyridin-1-ium

Base Information
  • Chemical Name:4-Nitro-2-(4-nitropyridin-2-yl)-1-oxidopyridin-1-ium
  • CAS No.:84175-12-2
  • Molecular Formula:C10H6N4O5
  • Molecular Weight:262.181
  • Hs Code.:2933399090
  • DSSTox Substance ID:DTXSID10402096
  • Wikidata:Q82205462
  • Mol file:84175-12-2.mol
4-Nitro-2-(4-nitropyridin-2-yl)-1-oxidopyridin-1-ium

Synonyms:4,4'-DINITRO-2,2'-BIPYRIDINE N-OXIDE;4-nitro-2-(4-nitropyridin-2-yl)-1-oxidopyridin-1-ium;84175-12-2;DTXSID10402096;AKOS024341067;J-400507;4-Nitro-2-(4-nitropyridin-2-yl)-1-oxo-1lambda~5~-pyridine

Suppliers and Price of 4-Nitro-2-(4-nitropyridin-2-yl)-1-oxidopyridin-1-ium
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
Total 4 raw suppliers
Chemical Property of 4-Nitro-2-(4-nitropyridin-2-yl)-1-oxidopyridin-1-ium
Chemical Property:
  • Vapor Pressure:3.91E-13mmHg at 25°C 
  • Boiling Point:586.8°C at 760 mmHg 
  • Flash Point:308.7°C 
  • PSA:129.99000 
  • Density:1.63g/cm3 
  • LogP:3.03990 
  • XLogP3:0.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:1
  • Exact Mass:262.03381930
  • Heavy Atom Count:19
  • Complexity:355
Purity/Quality:

95% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CN=C(C=C1[N+](=O)[O-])C2=[N+](C=CC(=C2)[N+](=O)[O-])[O-]
Technology Process of 4-Nitro-2-(4-nitropyridin-2-yl)-1-oxidopyridin-1-ium

There total 2 articles about 4-Nitro-2-(4-nitropyridin-2-yl)-1-oxidopyridin-1-ium 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 potassium nitrate; In sulfuric acid; for 24.5h; Heating;
DOI:10.1021/jo00151a001
Guidance literature:
Multi-step reaction with 2 steps
1: 62.6 percent / m-chloroperbenzoic acid / CHCl3 / 69 h / 0 °C
2: 40 percent / potassium nitrate / H2SO4 / 24.5 h / Heating
With potassium nitrate; 3-chloro-benzenecarboperoxoic acid; In chloroform; sulfuric acid;
DOI:10.1021/jo00151a001
Guidance literature:
With phosphorus trichloride; In chloroform; for 3h; Heating;
DOI:10.1021/jo00151a001
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