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2,4-Dichloro-6-(trifluoromethyl)quinoline is a synthetic organic compound with the molecular formula C11H5Cl2F3N. It belongs to the class of quinoline derivatives and is characterized by the presence of two chlorine atoms at the 2nd and 4th positions, and a trifluoromethyl group at the 6th position. This unique chemical structure endows it with diverse potential applications in various fields.

852203-17-9

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852203-17-9 Usage

Uses

Used in Pharmaceutical Industry:
2,4-Dichloro-6-(trifluoromethyl)quinoline is used as a building block for the synthesis of various drugs and pharmaceutical compounds. Its unique chemical structure allows for the development of new and effective medications.
Used in Antimicrobial Applications:
2,4-DICHLORO-6-(TRIFLUOROMETHYL)QUINOLINE has shown potential as an antimicrobial agent and is being studied for its activity against certain bacterial and fungal strains. Its ability to target and inhibit the growth of harmful microorganisms makes it a promising candidate for use in antimicrobial treatments.
Used in Agrochemical Industry:
2,4-Dichloro-6-(trifluoromethyl)quinoline may have applications in the field of agrochemicals, where it could be utilized to develop new pesticides or fungicides to protect crops and enhance agricultural productivity.
Used as a Reagent in Organic Synthesis:
Due to its unique chemical structure, 2,4-Dichloro-6-(trifluoromethyl)quinoline can also serve as a reagent in organic synthesis, enabling the creation of new compounds and materials with specific properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 852203-17-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,2,2,0 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 852203-17:
(8*8)+(7*5)+(6*2)+(5*2)+(4*0)+(3*3)+(2*1)+(1*7)=139
139 % 10 = 9
So 852203-17-9 is a valid CAS Registry Number.

852203-17-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 2,4-dichloro-6-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:852203-17-9 SDS

852203-17-9Relevant academic research and scientific papers

Acetonitrile-mediated synthesis of 2,4-dichloroquinoline from 2-ethynylaniline and 2,4-dichloroquinazoline from anthranilonitrile

Lee, Jae Hak,Lee, Byoung Se,Shin, Hyunik,Nam, Do Hyun,Chi, Dae Yoon

, p. 65 - 68 (2007/10/03)

2,4-Dichloroquinolines and 2,4-dichloroquinazolines were synthesized from 2-ethynylanilines and anthranilonitriles, respectively, using diphosgene in acetonitrile and heating at 130 °C or 150 °C for 12 hours. This reaction was applied to the synthesis of 4,6-dichloropyrazolo[3,4-d]pyrimidine (dichloro-9H-isopurine). The postulated mechanism is also described. Georg Thieme Verlag Stuttgart.

Microwave-assisted multistep synthesis of functionalized 4-arylquinolin-2(1H)-ones using palladium-catalyzed cross-coupling chemistry

Glasnov, Toma N.,Stadlbauer, Wolfgang,Kappe, C. Oliver

, p. 3864 - 3870 (2007/10/03)

Biologically active 4-aryl-3-alkenyl-substituted quinolin-2(1H)-ones have been synthesized in a short and concise manner employing readily available 4-hydroxyquinolin-2(1H)-ones as intermediates. Key steps in the synthesis include the derivatization of th

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