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1-butyl-4-hydroxy-2-quinolinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

296759-12-1

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296759-12-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 296759-12-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,6,7,5 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 296759-12:
(8*2)+(7*9)+(6*6)+(5*7)+(4*5)+(3*9)+(2*1)+(1*2)=201
201 % 10 = 1
So 296759-12-1 is a valid CAS Registry Number.

296759-12-1SDS

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 1-butyl-4-hydroxyquinolin-2-one

1.2 Other means of identification

Product number -
Other names 4-hydroxy-2-oxo-1-propyl-1,2-dihydroquinoline

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:296759-12-1 SDS

296759-12-1Downstream Products

296759-12-1Relevant academic research and scientific papers

4-Hydroxy-2-quinolones. 149*. Synthesis, chemical transformations, and biological properties of β-N-acylhydrazides of 1-R-4-hydroxy-2-oxo-1,2- dihydro-quinoline-4-carboxylic acids

Ukrainets,Tkach,Yang, Liu Yang

experimental part, p. 1347 - 1354 (2009/05/27)

Two methods of preparation have been proposed and the synthesis has been effected of a large series of β-N-acylhydrazides of 1-R-4-hydroxy-2-oxo-1, 2-dihydroquinoline-3-carboxylic acids. The possibility of using various condensing agents for converting them into the corresponding 1,3,4-oxa-diazoloquinolines has been studied. Results are given of an investigation of the antitubercular activity of the synthesized compounds.

METHOD FOR SCREENING CYSTEINE PROTEASE INHIBITOR

-

, (2008/06/13)

A method for screening a cysteine protease inhibitor of which cysteine protease inhibitory activity is enhanced in the presence of endogenous polyvalent metal ion, which comprises treating a cysteine protease with a test compound in the presence of the polyvalent metal ion, and a pharmaceutical composition for treating apoptosis-associated diseases, which contains as the active ingredient a cysteine protease inhibitor of which cysteine protease inhibitory activity is enhanced in the presence of endogenous polyvalent metal ion.

COMPOSITIONS FOR PREVENTING AND TREATING TYPE I ALLERGY

-

, (2008/06/13)

A method for screening a cysteine protease inhibitor of which cysteine protease inhibitory activity is enhanced in the presence of endogenous polyvalent metal ion, which comprises treating a cysteine protease with a test compound in the presence of the polyvalent metal ion, and a pharmaceutical composition for treating apoptosis-associated diseases, which contains as the active ingredient a cysteine protease inhibitor of which cysteine protease inhibitory activity is enhanced in the presence of endogenous polyvalent metal ion.

4-Hydroxy-2-quinolones. 42. Synthesis and biological activity of 1-R-2-oxo-3-(2H-1,2,4-benzothiadiazine-1,1-dioxid-3-yl)-4-hydroxyquinolines

Ukrainets,Taran,Gorokhova,Jaradat,Voronina,Porokhnyak

, p. 346 - 350 (2007/10/03)

A preparative method for the synthesis of 1-R-2-oxo-3-(2H-1,2,4-benzothiadiazine-l,l-dioxid-3-yl)-4-hydroxyquinolines has been developed. The diuretic and antitubercular activity of the obtained compounds have been studied.

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