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143946-48-9

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143946-48-9 Usage

General Description

4-Chloro-5-methylquinoline is a chemical compound with the molecular formula C10H8ClN. It is a yellowish powder that is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. 4-CHLORO-5-METHYLQUINOLINE is a quinoline derivative, which is a type of heterocyclic aromatic compound. Quinoline compounds have been studied for their potential anti-inflammatory, anti-cancer, and anti-malarial properties. 4-Chloro-5-methylquinoline is primarily used as a building block in the synthesis of other complex organic compounds, and its diverse applications make it an important compound in various chemical industries. It is important to handle this chemical with care, as it can be harmful if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 143946-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,9,4 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 143946-48:
(8*1)+(7*4)+(6*3)+(5*9)+(4*4)+(3*6)+(2*4)+(1*8)=149
149 % 10 = 9
So 143946-48-9 is a valid CAS Registry Number.

143946-48-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-CHLORO-5-METHYLQUINOLINE

1.2 Other means of identification

Product number -
Other names Quinoline,4-chloro-5-methyl

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:143946-48-9 SDS

143946-48-9Downstream Products

143946-48-9Relevant 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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