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1-Azido-4-nitrobenzene

Base Information
  • Chemical Name:1-Azido-4-nitrobenzene
  • CAS No.:1516-60-5
  • Molecular Formula:C6H4 N4 O2
  • Molecular Weight:164.123
  • Hs Code.:
  • European Community (EC) Number:841-636-6
  • NSC Number:118406
  • DSSTox Substance ID:DTXSID60164814
  • Wikidata:Q83033902
  • ChEMBL ID:CHEMBL3236181
  • Mol file:1516-60-5.mol
1-Azido-4-nitrobenzene

Synonyms:1-Azido-4-nitrobenzene;1516-60-5;Benzene, 1-azido-4-nitro-;diazonio-(4-nitrophenyl)azanide;p-Azidonitrobenzene;p-Nitrophenyl azide;4-Nitrophenyl azide;1-Azido-4-nitrobenzen;1-Nitro-4-triazobenzene;1-azido-4-nitro-benzene;CHEMBL3236181;SCHEMBL13449656;DTXSID60164814;BAA51660;NSC118406;AKOS016035723;NSC 118406;NSC-118406;1-(4-nitrophenyl)triaz-2-yn-2-ium-1-ide;EN300-133078

Suppliers and Price of 1-Azido-4-nitrobenzene
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 9 raw suppliers
Chemical Property of 1-Azido-4-nitrobenzene
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • Density:g/cm3 
  • XLogP3:2.8
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:1
  • Exact Mass:164.03342538
  • Heavy Atom Count:12
  • Complexity:210
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC(=CC=C1N=[N+]=[N-])[N+](=O)[O-]
Technology Process of 1-Azido-4-nitrobenzene

There total 74 articles about 1-Azido-4-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:
With hydroxylamine hydrochloride; In water; at 20 ℃; for 24h; Green chemistry;
DOI:10.1039/c6gc02379g
Guidance literature:
With dinitrogen tetraoxide; In tetrachloromethane; acetonitrile; at -30 ℃; for 0.166667h;
DOI:10.1016/S0040-4039(00)85055-8
Guidance literature:
With sodium azide; copper(II) acetate monohydrate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In dimethyl sulfoxide; at 95 ℃; for 2.5h;
DOI:10.3184/174751918X15260507766192
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