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4-Hydroxy-5-methylquinoline is an organic compound with the molecular formula C10H9NO. It is a derivative of quinoline, a heterocyclic aromatic compound consisting of a benzene ring fused to a pyridine ring. This particular compound features a hydroxyl group (-OH) at the 4-position and a methyl group (-CH3) at the 5-position. 4-Hydroxy-5-methylquinoline is a white crystalline solid that is soluble in organic solvents and has various applications in the chemical industry, including the synthesis of pharmaceuticals, agrochemicals, and dyes. It is also used as an intermediate in the production of certain antimalarial drugs and as a reagent in analytical chemistry. Due to its potential applications and properties, 4-hydroxy-5-methylquinoline is an important compound in the field of organic chemistry.

848128-81-4

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848128-81-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 848128-81-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,1,2 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 848128-81:
(8*8)+(7*4)+(6*8)+(5*1)+(4*2)+(3*8)+(2*8)+(1*1)=194
194 % 10 = 4
So 848128-81-4 is a valid CAS Registry Number.

848128-81-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-1H-quinolin-4-one

1.2 Other means of identification

Product number -
Other names 4-HYDROXY-5-METHYLQUINOLINE

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:848128-81-4 SDS

848128-81-4Downstream Products

848128-81-4Relevant articles and documents

Synthesis of ring-substituted 4-aminoquinolines and evaluation of their antimalarial activities

Madrid, Peter B.,Sherrill, John,Liou, Ally P.,Weisman, Jennifer L.,DeRisi, Joseph L.,Guy, R. Kiplin

, p. 1015 - 1018 (2007/10/03)

A simple two-step synthesis method was used to make 51 B-ring-substituted 4-hydroxyquinolines allowing analysis of the effect of ring substitutions on inhibition of growth of chloroquine sensitive and resistant strains of Plasmodium falciparum, the dominant cause of malaria morbidity. Substituted quinoline rings other than the 7-chloroquinoline ring found in chloroquine were found to have significant activity against the drug-resistant strain of P. falciparum W2.

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