3-Nitro-1-phenyl-4-phenylsulfanylquinolin-2-one

Base Information

Chemical Name:3-Nitro-1-phenyl-4-phenylsulfanylquinolin-2-one
CAS No.:141945-66-6
Molecular Formula:C21H14 N2 O3 S
Molecular Weight:374.4125
Hs Code.:
DSSTox Substance ID:DTXSID10359879
Wikidata:Q82141293
Mol file:141945-66-6.mol

Synonyms:3-nitro-1-phenyl-4-phenylsulfanylquinolin-2-one;3-nitro-1-phenyl-4-(phenylsulfanyl)-2(1H)-quinolinone;141945-66-6;AE-406/41056193;SCHEMBL13401415;DTXSID10359879

Suppliers and Price of 3-Nitro-1-phenyl-4-phenylsulfanylquinolin-2-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of 3-Nitro-1-phenyl-4-phenylsulfanylquinolin-2-one

Chemical Property:

Vapor Pressure:7.21E-11mmHg at 25°C
Boiling Point:518.8°C at 760 mmHg
Flash Point:267.6°C
PSA：93.12000
Density:1.42g/cm³
LogP:5.57330
XLogP3:4.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:374.07251349
Heavy Atom Count:27
Complexity:603

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)N2C3=CC=CC=C3C(=C(C2=O)[N+](=O)[O-])SC4=CC=CC=C4

Technology Process of 3-Nitro-1-phenyl-4-phenylsulfanylquinolin-2-one

There total 6 articles about 3-Nitro-1-phenyl-4-phenylsulfanylquinolin-2-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: 96.0%

: 110254-64-3
4-chloro-3-nitro-1-phenyl-2(1H)-quinolone

: 108-98-5
thiophenol

: 141945-66-6
3-nitro-1-phenyl-4-phenylthio-2(1H)-quinolone

Guidance literature:: With pyridine; In various solvent(s); for 0.5h; Ambient temperature;

Reference yield:

: 54675-12-6
4-hydroxy-3-nitro-1-phenyl-2(1H)-quinolone

: 141945-66-6
3-nitro-1-phenyl-4-phenylthio-2(1H)-quinolone

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / triethylamine, phosphoryl chloride / 1 h / Heating

2: 96 percent / pyridine / various solvent(s) / 0.5 h / Ambient temperature

With pyridine; triethylamine; trichlorophosphate; In various solvent(s);

Reference yield:

: 14994-75-3
4-hydroxy-1-phenylquinolin-2(1H)-one

: 141945-66-6
3-nitro-1-phenyl-4-phenylthio-2(1H)-quinolone

Guidance literature:: Multi-step reaction with 3 steps

1: 94 percent / conc. HNO₃, NaNO₂ / acetic acid / 0.5 h

2: 96 percent / triethylamine, phosphoryl chloride / 1 h / Heating

3: 96 percent / pyridine / various solvent(s) / 0.5 h / Ambient temperature

With pyridine; nitric acid; triethylamine; sodium nitrite; trichlorophosphate; In acetic acid;