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1,6-Diaminophenazine

Base Information
  • Chemical Name:1,6-Diaminophenazine
  • CAS No.:16582-03-9
  • Molecular Formula:C12H10 N4
  • Molecular Weight:210.23
  • Hs Code.:2933990090
  • DSSTox Substance ID:DTXSID20168030
  • Nikkaji Number:J3.059.354E
  • Wikidata:Q83037546
  • Mol file:16582-03-9.mol
1,6-Diaminophenazine

Synonyms:1,6-Diaminophenazine;1,6-Phenazinediamine;phenazine-1,6-diamine;16582-03-9;CCRIS 3023;Phenazine, 1,6-diamino-;BRN 0176444;FKTKBFVVAFESPW-UHFFFAOYSA-;DTXSID20168030;LS-103004

Suppliers and Price of 1,6-Diaminophenazine
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
  • American Custom Chemicals Corporation
  • 1,6-DIAMINOPHENAZINE 95.00%
  • 5MG
  • $ 496.89
Total 5 raw suppliers
Chemical Property of 1,6-Diaminophenazine
Chemical Property:
  • Vapor Pressure:1.83E-10mmHg at 25°C 
  • Boiling Point:508.6°Cat760mmHg 
  • Flash Point:294°C 
  • PSA:77.82000 
  • Density:1.414g/cm3 
  • LogP:3.10980 
  • XLogP3:1.3
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:0
  • Exact Mass:210.090546336
  • Heavy Atom Count:16
  • Complexity:231
Purity/Quality:

99% *data from raw suppliers

1,6-DIAMINOPHENAZINE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC(=C2C(=C1)N=C3C(=N2)C=CC=C3N)N
Technology Process of 1,6-Diaminophenazine

There total 3 articles about 1,6-Diaminophenazine 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; palladium on activated charcoal; In trifluoroacetic acid; for 2h;
DOI:10.1039/b506295k
Guidance literature:
Multi-step reaction with 2 steps
1: 30 percent / nitric acid; sulfuric acid / 8 h / 75 °C
2: 68 percent / H2 / Pd/C / trifluoroacetic acid / 2 h
With sulfuric acid; hydrogen; nitric acid; palladium on activated charcoal; In trifluoroacetic acid;
DOI:10.1039/b506295k
Guidance literature:
1,6-Dinitrophenazin, Zn-Staub, Red.;
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