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4,7-dichloro-3-methylquinoline is an organic compound characterized by its quinoline structure, which is a tricyclic aromatic system. This particular derivative features two chlorine atoms at the 4th and 7th positions and a methyl group at the 3rd position. It is a synthetic chemical that can be used in various applications, such as in the synthesis of pharmaceuticals or as an intermediate in chemical reactions. Due to its specific functional groups, it may exhibit different chemical properties compared to other quinolines. The compound's exact use and properties would depend on the context in which it is applied, and it is typically handled by professionals in a laboratory setting due to its potential reactivity and the need for controlled conditions.

6622-28-2

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6622-28-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6622-28-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6622-28:
(6*6)+(5*6)+(4*2)+(3*2)+(2*2)+(1*8)=92
92 % 10 = 2
So 6622-28-2 is a valid CAS Registry Number.

6622-28-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,7-dichloro-3-methylquinoline

1.2 Other means of identification

Product number -
Other names 4,7-dichloro-3-methyl-quinoline

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:6622-28-2 SDS

6622-28-2Relevant academic research and scientific papers

Antimalarials: Synthesis of 4-aminoquinolines that circumvent drug resistance in malaria parasites

De,Byers,Krogstad

, p. 315 - 320 (2007/10/03)

The strategies described here have permitted the synthesis of a series of 4-aminoquinoline antimalarials. Substantive improvements over previous syntheses include nucleophilic substitution with neat amine rather than in phenol, regioselective reductive alkylation to convert the terminal primary amine (12a-20a) on the diaminoalkane side chain to a diethylamino group, and purification by column chromatography with basic alumina. The 1H nmr spectra obtained after regioselective reductive alkylation with sodium borodeuteride (in comparison with sodium borohydride) demonstrated that this reductive alkylation proceeds via formation and subsequent reduction of the corresponding diamides in situ.

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