12H-Quino(2,1-b)quinazoline-5-carboxylic acid, 12-oxo-

Base Information

Chemical Name:12H-Quino(2,1-b)quinazoline-5-carboxylic acid, 12-oxo-
CAS No.:137522-63-5
Molecular Formula:C17H10N2O3
Molecular Weight:290.2729
Hs Code.:
DSSTox Substance ID:DTXSID20160211
Nikkaji Number:J418.773C
Wikidata:Q83028571

Synonyms:BRN 5442804;12H-Quino(2,1-b)quinazoline-5-carboxylic acid, 12-oxo-;Quinolino(2,1-b)quinazolin-12-one-5-carboxylic acid;12-Oxo-12H-quino(2,1-b)quinazoline-5-carboxylic acid;137522-63-5;12-Oxo-12H-quino[2,1-b]quinazoline-5-carboxylic acid;DTXSID20160211;LS-142948

Suppliers and Price of 12H-Quino(2,1-b)quinazoline-5-carboxylic acid, 12-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 0 raw suppliers

Chemical Property of 12H-Quino(2,1-b)quinazoline-5-carboxylic acid, 12-oxo-

Chemical Property:

Vapor Pressure:4.19E-10mmHg at 25°C
Boiling Point:482.1°C at 760 mmHg
Flash Point:245.4°C
Density:1.45g/cm³
XLogP3:1.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:290.06914219
Heavy Atom Count:22
Complexity:581

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C(=O)N3C4=CC=CC=C4C(=CC3=N2)C(=O)O

Technology Process of 12H-Quino(2,1-b)quinazoline-5-carboxylic acid, 12-oxo-

There total 1 articles about 12H-Quino(2,1-b)quinazoline-5-carboxylic acid, 12-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: 80.0%