Indolizino[2,3-g]quinoline-5,12-dione

Base Information

Chemical Name:Indolizino[2,3-g]quinoline-5,12-dione
CAS No.:915032-96-1
Molecular Formula:C₁₅H₈N₂O₂
Molecular Weight:248.241
Hs Code.:
ChEMBL ID:CHEMBL452698
DSSTox Substance ID:DTXSID60582110
Wikidata:Q82473431
Mol file:915032-96-1.mol

Synonyms:Indolizino[2,3-g]quinoline-5,12-dione;915032-96-1;CHEMBL452698;DTXSID60582110

Suppliers and Price of Indolizino[2,3-g]quinoline-5,12-dione

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
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price

Total 1 raw suppliers

Chemical Property of Indolizino[2,3-g]quinoline-5,12-dione

Chemical Property:

PSA：51.44000
LogP:2.10970
XLogP3:3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:248.058577502
Heavy Atom Count:19
Complexity:422

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=CC3=C(N2C=C1)C(=O)C4=C(C3=O)C=CC=N4

Technology Process of Indolizino[2,3-g]quinoline-5,12-dione

There total 3 articles about Indolizino[2,3-g]quinoline-5,12-dione 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: 82.0%

: 134793-78-5
ethyl 5,10-dioxo-5,10-dihydro-4a,6-diazabenzo[b]fluorene-11-carboxylate

: 915032-96-1
4,6-diazabenzo[b]fluorene-5,10-dione

Guidance literature:: ethyl 5,10-dioxo-5,10-dihydro-4a,6-diazabenzo[b]fluorene-11-carboxylate; With sodium hydroxide; In ethanol; for 0.5h; Heating;

With sodium ethanolate; In ethanol; for 5h; Heating;
DOI:10.1002/ejoc.200600317

Reference yield: 13.0%

: 110-86-1
pyridine

: 6541-19-1
6,7-dichloroquinoline-5,8-dione

: 75-52-5
nitromethane

: 915032-96-1
4,6-diazabenzo[b]fluorene-5,10-dione

: 1031265-44-7
C₁₅H₈N₂O₂

Guidance literature:: In ethanol; for 16h; Heating;
DOI:10.1016/j.bmc.2008.02.036

Reference yield:

: 6541-19-1
6,7-dichloroquinoline-5,8-dione

: 915032-96-1
4,6-diazabenzo[b]fluorene-5,10-dione

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium acetate / 2-methyl-propan-2-ol / 2 h / Heating

1.2: 4 h / Heating

2.1: NaOH / ethanol / 0.5 h / Heating

2.2: 82 percent / NaOEt / ethanol / 5 h / Heating

With sodium hydroxide; sodium acetate; In ethanol; tert-butyl alcohol;
DOI:10.1002/ejoc.200600317