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Cinnolin-8-amine

Base Information Edit
  • Chemical Name:Cinnolin-8-amine
  • CAS No.:21905-84-0
  • Molecular Formula:C8H7N3
  • Molecular Weight:145.16100
  • Hs Code.:2933990090
  • DSSTox Substance ID:DTXSID00506299
  • Nikkaji Number:J1.359.688C
  • Wikidata:Q82361995
  • Mol file:21905-84-0.mol
Cinnolin-8-amine

Synonyms:Cinnolin-8-amine;21905-84-0;8-Cinnolinamine;SCHEMBL1765856;DTXSID00506299;AKOS006339221;CS-0449648

Suppliers and Price of Cinnolin-8-amine
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
  • Crysdot
  • Cinnolin-8-amine 95+%
  • 1g
  • $ 1870.00
  • American Custom Chemicals Corporation
  • CINNOLIN-8-AMINE 95.00%
  • 5MG
  • $ 505.71
  • Alichem
  • Cinnolin-8-amine
  • 5g
  • $ 7372.74
  • Alichem
  • Cinnolin-8-amine
  • 1g
  • $ 2947.00
  • AccelPharmtech
  • 8-Cinnolinamine 97.00%
  • 25G
  • $ 12500.00
  • AccelPharmtech
  • 8-Cinnolinamine 97.00%
  • 5G
  • $ 4980.00
  • AccelPharmtech
  • 8-Cinnolinamine 97.00%
  • 1G
  • $ 3800.00
Total 4 raw suppliers
Chemical Property of Cinnolin-8-amine Edit
Chemical Property:
  • PSA:51.80000 
  • LogP:1.79320 
  • Storage Temp.:2-8°C 
  • XLogP3:0.5
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:0
  • Exact Mass:145.063997236
  • Heavy Atom Count:11
  • Complexity:137
Purity/Quality:

99%min *data from raw suppliers

Cinnolin-8-amine 95+% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC2=C(C(=C1)N)N=NC=C2
Technology Process of Cinnolin-8-amine

There total 10 articles about Cinnolin-8-amine 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 titanium(III) chloride; In acetic acid; at 11 ℃; for 0.116667h;
Guidance literature:
cinnoline-8-carboxylic acid; With diphenylphosphoranyl azide; triethylamine; In 1,4-dioxane; at 20 ℃; for 1.33333h;
With water; In 1,4-dioxane; at 100 ℃; for 48h;
Guidance literature:
Multi-step reaction with 8 steps
1.1: sulfuric acid / 16 h / 100 °C
2.1: sodium iodide; copper(l) iodide / 1,4-dioxane / 0.25 h / Sealed tube; Inert atmosphere
2.2: 16 h / 110 °C / Inert atmosphere
3.1: copper(l) iodide; triethylamine; bis-triphenylphosphine-palladium(II) chloride / acetonitrile / 3 h / 20 °C / Inert atmosphere
4.1: hydrogenchloride; sodium nitrite / water; tetrahydrofuran; acetonitrile / 0.25 h / -5 °C
4.2: 1.5 h / 0 - 20 °C
5.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 3 h / 0 - 20 °C
6.1: 1,2-dichloro-benzene / 0.5 h / 200 °C / Sealed tube
7.1: lithium hydroxide monohydrate / tetrahydrofuran / 3 h / 20 °C
8.1: triethylamine; diphenylphosphoranyl azide / 1,4-dioxane / 1.33 h / 20 °C
8.2: 48 h / 100 °C
With hydrogenchloride; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; lithium hydroxide monohydrate; sulfuric acid; diphenylphosphoranyl azide; tetrabutyl ammonium fluoride; triethylamine; sodium iodide; sodium nitrite; In tetrahydrofuran; 1,4-dioxane; water; 1,2-dichloro-benzene; acetonitrile;
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