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5-Quinolinecarboxylic acid, 8-methoxy-2-(trifluoromethyl)-, is a chemical compound with the molecular formula C13H8F3NO3. It is a derivative of quinolinecarboxylic acid, featuring a methoxy group and a trifluoromethyl group attached at specific positions on the quinoline ring. 5-Quinolinecarboxylic acid, 8-methoxy-2-(trifluoromethyl)has unique structural features and potential biological activity, making it a promising candidate for applications in medicinal chemistry and pharmaceutical development. Careful handling and adherence to safety protocols are essential when working with this chemical in a laboratory setting.

199872-29-2

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199872-29-2 Usage

Uses

Used in Medicinal Chemistry:
5-Quinolinecarboxylic acid, 8-methoxy-2-(trifluoromethyl)is used as a key intermediate in the synthesis of various pharmaceuticals for its unique structural features and potential biological activity.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 5-Quinolinecarboxylic acid, 8-methoxy-2-(trifluoromethyl)is utilized as a building block for the development of new drugs, particularly those targeting specific diseases or conditions. Its unique structure allows for the design of molecules with enhanced potency, selectivity, and pharmacokinetic properties.
Used in Drug Synthesis:
5-Quinolinecarboxylic acid, 8-methoxy-2-(trifluoromethyl)serves as a valuable precursor in the synthesis of various drug candidates, enabling the creation of novel therapeutic agents with improved efficacy and safety profiles.
Used in Drug Design:
5-Quinolinecarboxylic acid, 8-methoxy-2-(trifluoromethyl)is employed in the design of innovative drug molecules, leveraging its unique structural elements to create new chemical entities with potential therapeutic benefits.
Used in Research and Development:
5-Quinolinecarboxylic acid, 8-methoxy-2-(trifluoromethyl)is utilized in research and development laboratories to explore its potential applications and optimize its use in the creation of new pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 199872-29-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,8,7 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 199872-29:
(8*1)+(7*9)+(6*9)+(5*8)+(4*7)+(3*2)+(2*2)+(1*9)=212
212 % 10 = 2
So 199872-29-2 is a valid CAS Registry Number.

199872-29-2SDS

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 8-methoxy-2-(trifluoromethyl)quinoline-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 5-Quinolinecarboxylic acid,8-methoxy-2-(trifluoromethyl)

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:199872-29-2 SDS

199872-29-2Downstream Products

199872-29-2Relevant academic research and scientific papers

SYNTHESIS OF QUINOLINE 5-CARBOXAMIDES USEFUL FOR THE PREPARATION OF PDE IV INHIBITORS

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Page/Page column 22, (2010/02/11)

In one embodiment, the present application discloses a process for making the compound of the formula:

8-Methoxyquinolines as PDE4 inhibitors.

Billah, Motasim,Buckley, George M,Cooper, Nicola,Dyke, Hazel J,Egan, Robert,Ganguly, Ashit,Gowers, Lewis,Haughan, Alan F,Kendall, Hannah J,Lowe, Christopher,Minnicozzi, Michael,Montana, John G,Oxford, Janet,Peake, Joanna C,Picken, C Louise,Piwinski, John J,Naylor, Robert,Sabin, Verity,Shih, Neng-Yang,Warneck, Julie B H

, p. 1617 - 1619 (2007/10/03)

The synthesis and pharmacological profile of a novel series of 2-substituted 8-methoxyquinolines is described. The 2-trifluoromethyl compound was found to be a potent inhibitor of phosphodiesterase type 4 (PDE4).

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