3-Nitroquinoline 1-oxide

Base Information

Chemical Name:3-Nitroquinoline 1-oxide
CAS No.:7433-86-5
Molecular Formula:C9H6N2O3
Molecular Weight:190.158
Hs Code.:
DSSTox Substance ID:DTXSID50225342
Nikkaji Number:J59.545D
Wikidata:Q83104289
Mol file:7433-86-5.mol

Synonyms:3-Nitroquinoline 1-oxide;Quinoline, 3-nitro-, 1-oxide;BRN 0165282;7433-86-5;3-nitroquinoline-1-oxide;SCHEMBL11095195;DTXSID50225342;LS-142078;4-20-00-03396 (Beilstein Handbook Reference)

Suppliers and Price of 3-Nitroquinoline 1-oxide

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 3 raw suppliers

Chemical Property of 3-Nitroquinoline 1-oxide

Chemical Property:

Vapor Pressure:2.83E-06mmHg at 25°C
Boiling Point:400.9°Cat760mmHg
Flash Point:196.3°C
PSA：71.28000
Density:1.42g/cm³
LogP:2.69970
XLogP3:0.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:190.03784206
Heavy Atom Count:14
Complexity:229

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C=C(C=[N+]2[O-])[N+](=O)[O-]

Technology Process of 3-Nitroquinoline 1-oxide

There total 8 articles about 3-Nitroquinoline 1-oxide 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: 94.0%

: 1613-37-2
Quinoline N-oxide

: 7433-86-5
3-nitroquinoline N-oxide

Guidance literature:: With tert.-butylnitrite; In acetonitrile; at 100 ℃; for 24h; Reagent/catalyst; Solvent; Temperature; regioselective reaction; Green chemistry;
DOI:10.1039/c5ra04632g