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4-Bromo-7-chloro-2-(trifluoromethyl)quinoline is a heterocyclic aromatic compound that belongs to the quinoline family. It features a quinoline core with bromine, chlorine, and trifluoromethyl substituents, which contribute to its unique structure and properties. This chemical compound is a valuable intermediate in organic synthesis and has a wide range of applications in various research and industrial fields.

57124-19-3

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57124-19-3 Usage

Uses

Used in Synthetic Chemistry:
4-Bromo-7-chloro-2-(trifluoromethyl)quinoline is used as a building block in synthetic chemistry for the preparation of various biologically active compounds, pharmaceuticals, and agrochemicals. Its unique structure allows for the creation of diverse molecules with potential therapeutic and pesticidal properties.
Used in Coordination Chemistry as a Ligand:
In coordination chemistry, 4-Bromo-7-chloro-2-(trifluoromethyl)quinoline serves as a ligand, forming complexes with metal ions. These complexes exhibit interesting properties and can be used in various applications, such as catalysts, sensors, and materials with unique electronic or magnetic properties.
Used in Fluorescent Probes for Protein-Ligand Interactions:
4-Bromo-7-chloro-2-(trifluoromethyl)quinoline can be employed as a fluorescent probe for studying protein-ligand interactions. Its fluorescence properties allow researchers to monitor the binding of 4-Bromo-7-chloro-2-(trifluoromethyl)quinoline to target proteins, providing insights into the molecular mechanisms of action and potential applications in drug discovery.
Used in Research and Industrial Applications:
Due to its unique structure and properties, 4-Bromo-7-chloro-2-(trifluoromethyl)quinoline is a valuable intermediate in a variety of research and industrial applications. It can be used in the development of new synthetic routes, the synthesis of novel compounds with specific biological activities, and the exploration of its potential uses in various fields, such as materials science, pharmaceuticals, and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 57124-19-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,1,2 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 57124-19:
(7*5)+(6*7)+(5*1)+(4*2)+(3*4)+(2*1)+(1*9)=113
113 % 10 = 3
So 57124-19-3 is a valid CAS Registry Number.

57124-19-3SDS

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-bromo-7-chloro-2-(trifluoromethyl)quinoline

1.2 Other means of identification

Product number -
Other names 4-Brom-7-chlor-2-trifluormethylchinolin

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:57124-19-3 SDS

57124-19-3Upstream product

57124-19-3Downstream Products

57124-19-3Relevant academic research and scientific papers

Trifluoromethyl substituted analogs of quinine and quinidine

-

, (2008/06/13)

Trifluoromethyl substituted analogs of quinine and quinidine are prepared by reacting a 4-quinolyllithium compound with a 4,5-erythro-5-ethyl-(or vinyl)-quinuclidine-2 ξ-carboxaldehyde or the corresponding quinuclidine-2 ξ-carboxylic acid alkyl ester. The end products are useful as antimalarial agents.

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