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4(1H)-Quinolinone, 5-hydroxy-7-methoxy-3-(4-methoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

190774-08-4

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190774-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 190774-08-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,7,7 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 190774-08:
(8*1)+(7*9)+(6*0)+(5*7)+(4*7)+(3*4)+(2*0)+(1*8)=154
154 % 10 = 4
So 190774-08-4 is a valid CAS Registry Number.

190774-08-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-hydroxy-7-methoxy-3-(4-methoxyphenyl)-1H-quinolin-4-one

1.2 Other means of identification

Product number -
Other names 3-(4-methoxyphenyl)-5-hydroxy-7-methoxy-(1H)-quinolin-4-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:190774-08-4 SDS

190774-08-4Relevant academic research and scientific papers

Synthesis and anticancer evaluation of 3-substituted quinolin-4-ones and 2,3-dihydroquinolin-4-ones

Rajput, Santosh,Gardner, Christopher R.,Failes, Timothy W.,Arndt, Greg M.,Black, David Stc.,Kumar, Naresh

, p. 105 - 115 (2014/01/17)

A series of 3-aryl-5,7-dimethoxyquinolin-4-ones 8 and 3-aryl-5,7-dimethoxy- 2,3-dihydroquinolin-4-ones 13 were synthesized in good yields. Demethylation under a range of conditions afforded the corresponding 5-hydroxy and 5,7-dihydroxy derivatives. Biolog

Convenient synthetic routes to 5-substituted 3-(4-methoxyphenyl)-4(1H)-quinolones

Joseph, Beno?t,Béhard, Aurélie,Lesur, Brigitte,Guillaumet, Gérald

, p. 1542 - 1544 (2007/10/03)

5-Substituted 3-(4-methoxyphenyl)-4(1H)-quinolones 5-18 have been synthesised in good yields from the corresponding 3-(4-methoxyphenyl)-5-trifluoromethanesulfonate-4(1H)-quinolones 4 via palladium-mediated cross-coupling reactions or aromatic nucleophilic

Pharmaceutical compositions comprising 4-quinolones for treating cancers

-

, (2008/06/13)

A non-cytotoxic pharmaceutical composition acting on the proliferation of clonogenic cells in malignant tumors and including an efficient amount of a compound selected among the compounds of formula (I) and (Ia).

Synthesis of 3-(4-methoxyphenyl)-5,7-dimethoxy-(1H)-quinolin-2- or 4-ones and derivatives

Croisy, Martine,Huel, Christiane,Bisagni, Emile

, p. 683 - 690 (2007/10/03)

Condensation of ethyl 2-(4-methoxyphenyl)-3-hydroxyacrylate with 3,5-dimethoxyaniline afforded, depending on experimental conditions, either 3-(4-methoxyphenyl)-5,7-dimethoxy-(1H)-quinolin-2-one or 3-(4-methoxyphenyl)-5,7-dimethoxy-(1H)-quinolin-4-one. Whereas chlorination with phosphorous oxychloride led to the corresponding 2- and 4- chloroquinolines derivatives, 2-chloro-3-(4-methoxyphenyl)-5,7-dimethoxyquinoline was also obtained by using the Meth Cohn method's.

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