4-hydroxy-1-phenyl-3-(phenylsulfanyl)-2(1H)-quinolinone

Base Information

Chemical Name:4-hydroxy-1-phenyl-3-(phenylsulfanyl)-2(1H)-quinolinone
CAS No.:18693-16-8
Molecular Formula:C21H15NO2S
Molecular Weight:345.4143
Hs Code.:
Mol file:18693-16-8.mol

Synonyms:4-Hydroxy-1-phenyl-3-phenylsulfanyl-1H-quinolin-2-one;4-hydroxy-1-phenyl-3-phenylthio-2(1H)-quinolone;

Suppliers and Price of 4-hydroxy-1-phenyl-3-(phenylsulfanyl)-2(1H)-quinolinone

Supply Marketing:

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

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Chemical Property of 4-hydroxy-1-phenyl-3-(phenylsulfanyl)-2(1H)-quinolinone

Chemical Property:

Vapor Pressure:7.91E-10mmHg at 25°C
Boiling Point:475°Cat760mmHg
Flash Point:241.1°C
PSA：67.53000
Density:1.39g/cm³
LogP:4.84750

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 4-hydroxy-1-phenyl-3-(phenylsulfanyl)-2(1H)-quinolinone

There total 3 articles about 4-hydroxy-1-phenyl-3-(phenylsulfanyl)-2(1H)-quinolinone 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: 72.0%

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

: 882-33-7
diphenyldisulfane

: 18693-16-8
4-hydroxy-1-phenyl-3-phenylsulfanylquinolin-2(1H)-one

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 100 - 130 ℃; for 5h;
DOI:10.1002/jhet.5570390621

Reference yield:

: 2-[Phenyl-(2-phenylsulfanyl-acetyl)-amino]-benzoic acid methyl ester

: 18693-16-8
4-hydroxy-1-phenyl-3-phenylsulfanylquinolin-2(1H)-one

Guidance literature:: With Amberlyst A-26 (OH(-) form); trifluoroacetic acid; Yield given. Multistep reaction; 1.) MeOH, r.t., 16 h, 2.) MeOH, r.t., 30 min;
DOI:10.1039/a709125g