4H-Imidazo[4,5,1-ij]quinolin-2(1H)-one

Base Information

Chemical Name:4H-Imidazo[4,5,1-ij]quinolin-2(1H)-one
CAS No.:83848-83-3
Molecular Formula:C10H8 N2 O
Molecular Weight:0
Hs Code.:2933990090
DSSTox Substance ID:DTXSID10509918
Mol file:83848-83-3.mol

Synonyms:4H-Imidazo[4,5,1-ij]quinolin-2(1H)-one;83848-83-3;4h-imidazo(4,5,1-ij)quinolin-2(1h)-one;1,2-Dihydro-4-imidazo{4,5,1-i,j}quinolin-2-one;SCHEMBL1650468;DTXSID10509918;QBRFYQULBWCTPB-UHFFFAOYSA-N;AKOS024288542

Suppliers and Price of 4H-Imidazo[4,5,1-ij]quinolin-2(1H)-one

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 4 raw suppliers

Chemical Property of 4H-Imidazo[4,5,1-ij]quinolin-2(1H)-one

Chemical Property:

PSA：38.05000
LogP:1.76870
XLogP3:1.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:172.063662883
Heavy Atom Count:13
Complexity:274

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C=CC2=C3N1C(=O)NC3=CC=C2

Technology Process of 4H-Imidazo[4,5,1-ij]quinolin-2(1H)-one

There total 2 articles about 4H-Imidazo[4,5,1-ij]quinolin-2(1H)-one 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: 47.6%

: 83848-82-2
quinolin-8-ylcarbamic acid phenyl ester

: 83848-83-3
1,2-dihydro-4H-imidazo<5,4,1-ij>quinolin-2-one

Guidance literature:: With sodium tetrahydroborate; In tetrahydrofuran; ethanol; for 20h; Ambient temperature;

Reference yield:

: 578-66-5
8-amino quinoline

: 83848-83-3
1,2-dihydro-4H-imidazo<5,4,1-ij>quinolin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 86.4 percent / pyridine / 72 h / Ambient temperature

2: 47.6 percent / NaBH₄ / ethanol; tetrahydrofuran / 20 h / Ambient temperature

With pyridine; sodium tetrahydroborate; In tetrahydrofuran; ethanol;