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2-TRIFLUOROMETHYLQUINOLINE-7-CARBOXYLIC ACID, also known as 2-trifluoromethyl-7-quinolinecarboxylic acid, is a chemical compound with the molecular formula C11H6F3NO2. It is a derivative of quinoline and contains a carboxylic acid functional group and a trifluoromethyl group. 2-TRIFLUOROMETHYLQUINOLINE-7-CARBOXYLIC ACID has been studied for its potential use in pharmaceuticals, agrochemicals, and organic electronics due to its fluorescent properties. It has also been found to exhibit antiangiogenic and antiproliferative effects, making it a potential candidate for cancer therapy. Additionally, 2-trifluoromethylquinoline-7-carboxylic acid has been investigated for its antimicrobial and antibacterial properties, which could have applications in the development of new antibiotics.

868662-63-9

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868662-63-9 Usage

Uses

Used in Pharmaceutical Industry:
2-TRIFLUOROMETHYLQUINOLINE-7-CARBOXYLIC ACID is used as a potential therapeutic agent for cancer treatment due to its antiangiogenic and antiproliferative effects. It targets the inhibition of blood vessel formation and the proliferation of cancer cells, making it a promising candidate for cancer therapy.
Used in Agrochemical Industry:
2-TRIFLUOROMETHYLQUINOLINE-7-CARBOXYLIC ACID is used as a potential active ingredient in agrochemicals, where its properties can be harnessed to develop new pesticides or herbicides.
Used in Organic Electronics:
2-TRIFLUOROMETHYLQUINOLINE-7-CARBOXYLIC ACID is used as a component in organic electronics due to its fluorescent properties, which can be utilized in the development of advanced electronic devices and materials.
Used in Antibacterial Applications:
2-TRIFLUOROMETHYLQUINOLINE-7-CARBOXYLIC ACID is used as a potential antimicrobial and antibacterial agent in the development of new antibiotics, given its ability to combat bacterial infections and contribute to the discovery of novel antimicrobial compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 868662-63-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,6,6 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 868662-63:
(8*8)+(7*6)+(6*8)+(5*6)+(4*6)+(3*2)+(2*6)+(1*3)=229
229 % 10 = 9
So 868662-63-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H6F3NO2/c12-11(13,14)9-4-3-6-1-2-7(10(16)17)5-8(6)15-9/h1-5H,(H,16,17)

868662-63-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(trifluoromethyl)quinoline-7-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-Trifluoromethylquinoline-7-carboxylic acid

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:868662-63-9 SDS

868662-63-9Upstream product

868662-63-9Downstream Products

868662-63-9Relevant academic research and scientific papers

New regiospecific synthesis of 2-trifluoromethyl-1,5 diazapentadiene compounds and of 2-trifluoromethylquinolines, their cyclization products

El Kharrat, Salem,Skander, Myriem,Dahmani, Abdelkader,Laurent, Philippe,Blancou, Hubert

, p. 8327 - 8331 (2005)

2-Trifluoromethylquinolines 5 are synthesized in high yields using a perfluoroalkylated gemiodoacetoxy derivative 3 and arylamines 4. The intermediate of this reaction, 2-trifluoromethyl-1,5-diazapentadiene compound 6, was isolated. The procedures are eas

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