1H-Pyrazolo(3,4-f)quinoline-8-carboxylic acid, 6,9-dihydro-6-ethenyl-9-oxo-

Base Information

Chemical Name:1H-Pyrazolo(3,4-f)quinoline-8-carboxylic acid, 6,9-dihydro-6-ethenyl-9-oxo-
CAS No.:69847-87-6
Molecular Formula:C13H9N3O3
Molecular Weight:255.2289
Hs Code.:
DSSTox Substance ID:DTXSID00220145
Wikidata:Q83097251

Synonyms:BRN 0811410;1-Vinyl-3-carboxy-4-oxo-pyrazolo(5,4-f)quinoline;1H-Pyrazolo(3,4-f)quinoline-8-carboxylic acid, 6,9-dihydro-6-ethenyl-9-oxo-;1-Vinyl-3-carboxy-4-oxo-pyrazol(5,4-f)chinolin [German];6,9-Dihydro-6-ethenyl-9-oxo-1H-pyrazolo(3,4-f)quinoline-8-carboxylic acid;Acide dihydro-6,9 oxo-9 vinyl-6 pyrazolo(5,4-f)quinoleine carboxylique-8 [French];1-Vinyl-3-carboxy-4-oxo-pyrazol(5,4-f)chinolin;69847-87-6;Acide dihydro-6,9 oxo-9 vinyl-6 pyrazolo(5,4-f)quinoleine carboxylique-8;DTXSID00220145;LS-129322

Suppliers and Price of 1H-Pyrazolo(3,4-f)quinoline-8-carboxylic acid, 6,9-dihydro-6-ethenyl-9-oxo-

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 2 raw suppliers

Chemical Property of 1H-Pyrazolo(3,4-f)quinoline-8-carboxylic acid, 6,9-dihydro-6-ethenyl-9-oxo-

Chemical Property:

Vapor Pressure:9.22E-11mmHg at 25°C
Boiling Point:498.6°Cat760mmHg
Flash Point:255.4°C
Density:1.658g/cm³
XLogP3:2.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:255.06439116
Heavy Atom Count:19
Complexity:474

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=CN1C=C(C(=O)C2=C1C=CC3=C2NN=C3)C(=O)O

Technology Process of 1H-Pyrazolo(3,4-f)quinoline-8-carboxylic acid, 6,9-dihydro-6-ethenyl-9-oxo-

There total 4 articles about 1H-Pyrazolo(3,4-f)quinoline-8-carboxylic acid, 6,9-dihydro-6-ethenyl-9-oxo- 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:

: 6967-12-0
6-amino-1H-indazole

: 69847-87-6
acide dihydro-6,9 oxo-9 vinyl-6 pyrazolo <5.4-f>quinoleine carboxylique-8

Guidance literature:: Multi-step reaction with 3 steps

1: 75 percent / 0.5 h / 110 °C

2: 90 percent / Gilotherm / 0.17 h / 255 °C

3: 1.) K₂CO₃; 2.) 10percent NaOH / 1.) dimethylformamide, 70 deg C; 2.) reflux, 0.5-2 h

With sodium hydroxide; potassium carbonate;

Reference yield:

: 65642-21-9
indazolyl-6 aminomethyllenemalonate d'ethyle

: 69847-87-6
acide dihydro-6,9 oxo-9 vinyl-6 pyrazolo <5.4-f>quinoleine carboxylique-8

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / Gilotherm / 0.17 h / 255 °C

2: 1.) K₂CO₃; 2.) 10percent NaOH / 1.) dimethylformamide, 70 deg C; 2.) reflux, 0.5-2 h

With sodium hydroxide; potassium carbonate;

Reference yield:

: 107-04-0
1-Bromo-2-chloroethane

: 65642-22-0
ester ethylique de l'acide dihydro-6,9 oxo-9 pyrazolo <5.4-f>quinoleine carboxylique

: 69847-87-6
acide dihydro-6,9 oxo-9 vinyl-6 pyrazolo <5.4-f>quinoleine carboxylique-8

Guidance literature:: With sodium hydroxide; potassium carbonate; Yield given. Multistep reaction; 1.) dimethylformamide, 70 deg C; 2.) reflux, 0.5-2 h;