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4-Chloro-6-fluoro-2-(trifluoromethyl)quinoline, a quinoline derivative with the molecular formula C11H5ClF4N, is characterized by a chloro-substituted ring at the 4 position, a fluoro-substituted ring at the 6 position, and a trifluoromethyl group at the 2 position. This chemical compound is frequently utilized in pharmaceutical research and development as a key building block for synthesizing a variety of bioactive compounds. Its quinoline structure, a common feature in numerous anti-malarial drugs, has also garnered interest for its potential as an anti-malarial agent. Furthermore, it has demonstrated antimicrobial and anti-cancer properties, positioning it as a significant chemical for further exploration and possible applications within the medical and pharmaceutical sectors.

59611-55-1

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59611-55-1 Usage

Uses

Used in Pharmaceutical Research and Development:
4-Chloro-6-fluoro-2-(trifluoromethyl)quinoline is used as a building block for the synthesis of various bioactive compounds, contributing to the development of new pharmaceuticals with potential therapeutic applications.
Used in Anti-malarial Drug Development:
Leveraging its quinoline structure, 4-Chloro-6-fluoro-2-(trifluoromethyl)quinoline is studied for its potential use as an anti-malarial agent, given the prevalence of quinoline motifs in existing anti-malarial medications.
Used in Antimicrobial Applications:
4-Chloro-6-fluoro-2-(trifluoromethyl)quinoline is employed for its antimicrobial properties, offering a potential solution in the ongoing battle against resistant bacteria and other microorganisms.
Used in Anti-cancer Research:
4-CHLORO-6-FLUORO-2-(TRIFLUOROMETHYL)QUINOLINE is utilized in anti-cancer research to explore its potential to combat cancer cells, adding to the arsenal of tools available for cancer treatment and management.
Used in the Medical and Pharmaceutical Industries:
4-Chloro-6-fluoro-2-(trifluoromethyl)quinoline is valued for its broad-spectrum applications in the medical and pharmaceutical industries, where it can be further investigated and developed into effective treatments and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 59611-55-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,6,1 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 59611-55:
(7*5)+(6*9)+(5*6)+(4*1)+(3*1)+(2*5)+(1*5)=141
141 % 10 = 1
So 59611-55-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H23O.CHF3O3S/c1-10-8-11(13(2,3)4)15-12(9-10)14(5,6)7;2-1(3,4)8(5,6)7/h8-9H,1-7H3;(H,5,6,7)/q+1;/p-1

59611-55-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-CHLORO-6-FLUORO-2-(TRIFLUOROMETHYL)QUINOLINE

1.2 Other means of identification

Product number -
Other names 4-chloro-6-fluoro-2-trifluoromethylquinoline

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:59611-55-1 SDS

59611-55-1Upstream product

59611-55-1Downstream Products

59611-55-1Relevant academic research and scientific papers

2 -trifluoromethyl -4 - amino - quinoline derivative and application thereof

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Paragraph 0092-0096; 0168-0172, (2021/11/10)

The invention discloses 2 -trifluoromethyl -4 - amino - quinoline derivatives and application thereof, and comprises a compound represented by the following general formula I. The prepared compound is used for preparing an anti-tumor active drug, has a go

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