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2-CHLORO-4-METHOXYQUINOLINE is a chloro-substituted quinoline derivative with a molecular formula C10H8ClNO. It features a chlorine atom at the 2-position and a methoxy group at the 4-position of the quinoline ring. This chemical compound has garnered interest due to its potential pharmaceutical applications, such as antimalarial and antimicrobial properties, and its utility as a building block in the synthesis of other biologically active compounds. Furthermore, it has been explored for its potential as a fluorescent probe in biological imaging studies.

4295-09-4

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4295-09-4 Usage

Uses

Used in Pharmaceutical Industry:
2-CHLORO-4-METHOXYQUINOLINE is used as a pharmaceutical compound for its antimalarial and antimicrobial properties, offering potential treatments for various diseases caused by these pathogens.
Used in Chemical Synthesis:
2-CHLORO-4-METHOXYQUINOLINE is used as a building block in the synthesis of other biologically active compounds, contributing to the development of new pharmaceuticals and therapeutic agents.
Used in Biomedical Research:
2-CHLORO-4-METHOXYQUINOLINE is used as a fluorescent probe in biological imaging studies, aiding researchers in visualizing and studying biological processes at the molecular level.

Check Digit Verification of cas no

The CAS Registry Mumber 4295-09-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,9 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4295-09:
(6*4)+(5*2)+(4*9)+(3*5)+(2*0)+(1*9)=94
94 % 10 = 4
So 4295-09-4 is a valid CAS Registry Number.

4295-09-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-4-methoxyquinoline

1.2 Other means of identification

Product number -
Other names 2-Chloro-4-methoxy-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:4295-09-4 SDS

4295-09-4Upstream product

4295-09-4Downstream Products

4295-09-4Relevant academic research and scientific papers

Synthesis and characterization of substituted 4-methoxy-1H-quinolin-2- thiones

Ramasamy,Balasubramaniam,Mohan

, p. 4726 - 4728 (2012/09/07)

The synthesis of various substituted 4-methoxy-1H-quinolin-2-thiones from various substituted aniline with malonic acid, phosphorousoxychloride, sodium methoxide glacial acetic acid and thiourea under different conditions is described. All these substituted 4-methoxy-1H-quinolin-2-thiones were synthesized from four steps; the first step involved the synthesis of substituted 2,4-dichloro quinoline from aniline (substituted), with malonic acid and phosphorous-oxychloride. In the second step, the substituted 2,4-dichloro compound was heated with freshly prepared methanolic sodium methoxide solution to give 2,4-dimethoxy quinoline compounds, it was then refluxed with glacial acetic acid and hydrochloric acid to get the substituted 4-methoxy-1H-quinolin- 2-one. The final steps involves with an objective of introducing a chloro in the position 2 of the quinolone system, the substituted 4-methoxy-1H-quinolin-2-one was refluxed with distilled PoCl3 chloroform. The substituted 2-chloro-4-methoxy quinoline was then refluxed with thiourea and alcohol to get substituted 4-methoxy-1H-quinolin-2-thiones. The purity of the synthesized compound was judged by their C, H and N analysis and the structure was analyzed on the basics of mass, FT-IR and 1H NMR.

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