Dibenzo[b,g][1,5]naphthyridine-6,12(5H,11H)-dione

Base Information

Chemical Name:Dibenzo[b,g][1,5]naphthyridine-6,12(5H,11H)-dione
CAS No.:17352-37-3
Molecular Formula:C16H10N2O2
Molecular Weight:0
Hs Code.:
Mol file:17352-37-3.mol

Synonyms:Dibenzo{b,g}{1,5}-naphthiridin-6,12(5,11H)dion;5,11-Dihydro-dibenzo[b,g][1,5]naphthyridine-6,12-dione;epindolidione;5,11-Dihydro-dibenzo[b,g][1,5]naphthyridin-6,12-dion;Epindolidion, 5H,11H-Dibenzo1,5-naphthyridindion-(6,12);

Suppliers and Price of Dibenzo[b,g][1,5]naphthyridine-6,12(5H,11H)-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
Packaging
price

Total 5 raw suppliers

Chemical Property of Dibenzo[b,g][1,5]naphthyridine-6,12(5H,11H)-dione

Chemical Property:

PSA：65.72000
LogP:2.52280

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Dibenzo[b,g][1,5]naphthyridine-6,12(5H,11H)-dione

There total 7 articles about Dibenzo[b,g][1,5]naphthyridine-6,12(5H,11H)-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: 80.0%

: 482-89-3,12626-73-2
1H,1H'-2,2'-Biindolylidene-3,3'-dione

: 17352-37-3
dibenzo{b,g}{1,5}-naphthiridin-6,12(5,11H)-dione

Guidance literature:: In gas; at 460 ℃;

Reference yield:

: 860367-74-4
3-anilino-4-hydroxy-quinoline-2-carboxylic acid

: 17352-37-3
dibenzo{b,g}{1,5}-naphthiridin-6,12(5,11H)-dione

Guidance literature:: With phosphorus pentoxide; nitrobenzene;
DOI:10.1002/hlca.19480310306

Reference yield:

: 401640-33-3
(2-acetyl-phenyl)-oxalamic acid ethyl ester

: 17352-37-3
dibenzo{b,g}{1,5}-naphthiridin-6,12(5,11H)-dione

Guidance literature:: Multi-step reaction with 4 steps

1: chloroform; bromine / Irradiation

2: ethanol

3: aq.-ethanolic NaOH

4: P₂O₅; nitrobenzene

With sodium hydroxide; ethanol; chloroform; bromine; phosphorus pentoxide; nitrobenzene;
DOI:10.1002/hlca.19480310306