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4,6-Dichloro-2-(trifluoromethyl)quinoline is a quinoline derivative chemical compound composed of carbon, hydrogen, chlorine, and fluorine atoms. It features a quinoline ring with two chloro groups and one trifluoromethyl group attached, which endows it with unique structural features and reactivity. These characteristics make it a valuable component in the synthesis of new compounds for potential applications in medicinal and agricultural fields, as well as in material science and chemical research.

18706-33-7

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18706-33-7 Usage

Uses

Used in Pharmaceutical Development:
4,6-Dichloro-2-(trifluoromethyl)quinoline is used as a key intermediate in the synthesis of pharmaceutical compounds for various therapeutic applications. Its unique structure allows for the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Synthesis:
In the agrochemical industry, 4,6-dichloro-2-(trifluoromethyl)quinoline serves as a building block for the creation of novel agrochemicals. Its incorporation into these compounds can lead to the development of more effective and targeted pesticides and other agricultural products.
Used in Material Science:
4,6-Dichloro-2-(trifluoromethyl)quinoline may also find applications in material science due to its potential to form new materials with unique properties. Its structural features can contribute to the development of advanced materials for various industrial and technological applications.
Used in Chemical Research:
As a quinoline derivative with specific reactivity, 4,6-dichloro-2-(trifluoromethyl)quinoline is utilized in chemical research to explore new reaction pathways and mechanisms. This can lead to the discovery of innovative synthetic methods and the creation of novel compounds with potential applications across various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 18706-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,0 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 18706-33:
(7*1)+(6*8)+(5*7)+(4*0)+(3*6)+(2*3)+(1*3)=117
117 % 10 = 7
So 18706-33-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H4Cl2F3N/c11-6-3-1-2-5-7(12)4-8(10(13,14)15)16-9(5)6/h1-4H

18706-33-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-DICHLORO-2-(TRIFLUOROMETHYL)QUINOLINE

1.2 Other means of identification

Product number -
Other names 4,6-Dichloro-2-trifluoromethyl-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:18706-33-7 SDS

18706-33-7Downstream Products

18706-33-7Relevant academic research and scientific papers

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

-

Paragraph 0092-0096; 0148-0152, (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

Palladium-catalyzed chloroimination of imidoyl chlorides to a triple bond: An intramolecular reaction leading to 4-chloroquinolines

Isobe, Akira,Takagi, Jun,Katagiri, Toshimasa,Uneyama, Kenji

supporting information; experimental part, p. 2657 - 2659 (2009/05/27)

(Chemical Equation Presented) In this paper, a new type of effective chloroimination was reported. This reaction afforded 4-chloro-2-perfluoroalkyl quinolines from fluorinated imidoyl chlorides in high yields. This is the first achievement of oxidative addition-reductive elimination type C-Cl bond activation by chloropalladation.

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