Quinoxalino[2,3-c]cinnoline

Base Information

Chemical Name:Quinoxalino[2,3-c]cinnoline
CAS No.:75608-87-6
Molecular Formula:C₁₄H₈N₄
Molecular Weight:232.244
Hs Code.:
DSSTox Substance ID:DTXSID60363360
Nikkaji Number:J743.760I
Wikidata:Q82147027
ChEMBL ID:CHEMBL578516
Mol file:75608-87-6.mol

Synonyms:quinoxalino[2,3-c]cinnoline;75608-87-6;5,6,7,12-TETRAAZATETRAPHENE;GNF-Pf-2434;cinnolino[4,3-b]quinoxaline;CHEMBL578516;DTXSID60363360;5,6,7,12-Tetraazabenz[a]anthracene;AKOS005103245;8L-708

Suppliers and Price of Quinoxalino[2,3-c]cinnoline

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
QUINOXALINO[2,3-C]CINNOLINE 95.00%
5MG
$ 623.82

American Custom Chemicals Corporation
QUINOXALINO[2,3-C]CINNOLINE 95.00%
10MG
$ 618.50

American Custom Chemicals Corporation
QUINOXALINO[2,3-C]CINNOLINE 95.00%
1MG
$ 586.97

Total 1 raw suppliers

Chemical Property of Quinoxalino[2,3-c]cinnoline

Chemical Property:

PSA：51.56000
LogP:2.72620
XLogP3:2.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:0
Exact Mass:232.074896272
Heavy Atom Count:18
Complexity:308

Purity/Quality:: QUINOXALINO[2,3-C]CINNOLINE 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)C3=NC4=CC=CC=C4N=C3N=N2

Technology Process of Quinoxalino[2,3-c]cinnoline

There total 7 articles about Quinoxalino[2,3-c]cinnoline 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:

Reference yield: 52.0%

: 151-50-8
potassium cyanide

: 113001-01-7
o-acetamide-N-(o-nitrobenzylidene)aniline

: 75608-87-6
quinoxalino<2,3-c>cinnoline

Guidance literature:: In methanol; for 3h; Heating;

Reference yield:

: 552-32-9
o-nitroacetanilide

: 75608-87-6
quinoxalino<2,3-c>cinnoline

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent / hydrogen / 10percent palladium-charcoal / methanol

2: 82 percent / ethanol / 0.17 h

3: 52 percent / methanol / 3 h / Heating

With ethanol; hydrogen; palladium on activated charcoal; In methanol;