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4-Hydroxy-3,5-dinitrobenzonitrile

Base Information
  • Chemical Name:4-Hydroxy-3,5-dinitrobenzonitrile
  • CAS No.:2315-80-2
  • Molecular Formula:C7H3 N3 O5
  • Molecular Weight:209.1158
  • Hs Code.:2926909090
  • DSSTox Substance ID:DTXSID10177732
  • Nikkaji Number:J2.667.294E
  • Wikidata:Q83048057
  • Mol file:2315-80-2.mol
4-Hydroxy-3,5-dinitrobenzonitrile

Synonyms:4-Hydroxy-3,5-dinitrobenzonitrile;2315-80-2;Benzonitrile, 4-hydroxy-3,5-dinitro-;C7H3N3O5;DTXSID10177732;3,5-Dinitro-4-hydroxybenzonitrile;C7-H3-N3-O5;3,5-dinitro-4-hydroxy benzonitrile;FT-0743376;A18491

Suppliers and Price of 4-Hydroxy-3,5-dinitrobenzonitrile
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 8 raw suppliers
Chemical Property of 4-Hydroxy-3,5-dinitrobenzonitrile
Chemical Property:
  • Vapor Pressure:0.00254mmHg at 25°C 
  • Boiling Point:278.3°Cat760mmHg 
  • Flash Point:122.1°C 
  • PSA:135.66000 
  • Density:1.72g/cm3 
  • LogP:2.12668 
  • XLogP3:0.8
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:0
  • Exact Mass:209.00727020
  • Heavy Atom Count:15
  • Complexity:300
Purity/Quality:

97% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=C(C=C(C(=C1[N+](=O)[O-])O)[N+](=O)[O-])C#N
Technology Process of 4-Hydroxy-3,5-dinitrobenzonitrile

There total 2 articles about 4-Hydroxy-3,5-dinitrobenzonitrile 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 trichloroisocyanuric acid; silica gel; sodium nitrite; at 20 ℃; for 0.25h;
DOI:10.1055/s-2003-42063
Guidance literature:
With potassium hydroxide; In methanol; water; at 25 ℃; Rate constant; μ = 0.2 M (KCl), hydrolysis; reactivity of spiro, 1,1-dimethoxy, and 1-methoxy-1-phenoxy Meisenheimer complexes, stereoelectronic and conformational effects;
DOI:10.1021/ja00389a057
upstream raw materials:

2,6-dinitro-4-cyanoanisole

4-cyanophenol

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