92513-28-5

Usage

Uses

Used in Pharmaceutical Industry:
3-Methylquinoline-2-carboxylic acid is used as an intermediate in the synthesis of various pharmaceuticals for its potential pharmacological activities. It contributes to the development of drugs that target the inhibition of cancer cell growth, making it a valuable component in anticancer drug discovery and formulation.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Methylquinoline-2-carboxylic acid serves as an essential intermediate in the production of agrochemicals, which are utilized in pest control and crop protection. Its role in this industry is pivotal for creating effective and targeted solutions to enhance agricultural productivity.
Used in Dye and Pigment Production:
3-Methylquinoline-2-carboxylic acid is used as a building block in the creation of dyes and pigments for various applications. Its chemical properties make it suitable for the development of colorants that are stable and vibrant, serving the needs of industries such as textiles, plastics, and printing inks.
Used in Research Applications:
3-Methylquinoline-2-carboxylic acid is utilized in research settings to explore its pharmacological properties further. It is an important compound for scientific investigations into its anti-inflammatory effects and its potential role in the development of new therapeutic agents.
Production Methods:
3-Methylquinoline-2-carboxylic acid is typically produced through multistep organic synthesis techniques, which involve a series of chemical reactions to obtain the desired compound. It is commercially available for research and industrial use, ensuring that it can be accessed by professionals in various fields for their specific applications.

InChI:InChI=1/C11H9NO2/c1-7-6-8-4-2-3-5-9(8)12-10(7)11(13)14/h2-6H,1H3,(H,13,14)

Upstream product

• 27356-52-1 2-ethyl-3-methylquinoline 
• 860718-13-4 3-methyl-2-tribromomethyl-quinoline 
• 600-18-0 2-Oxobutyric acid 
• 529-23-7 o-aminobenzaldehyde 
• 1721-89-7 2,3-dimethylquinoline 
• 552-89-6 2-nitro-benzaldehyde 

Downstream Products

• 643-38-9 quinoline-2,3-dicarboxylic acid 
• 53821-46-8 methyl 3-methylquinoline-2-carboxylate 
• 55854-89-2 8-methyl-7-propionylindolizino[1,2-b]quinoline-9(11H)-one 
• 54318-59-1 (S)-mappicine 

Relevant academic research and scientific papers

Total synthesis of nothapodytine b and (-)-mappicine

Concise total syntheses of naturally occurring nothapodytine B (1, mappicine ketone) and ( - )-mappicine (3) are detailed. The approach is based on the implememation of a room-temperature, inverse electron demand Diels-Alder reaction of the N-sulfonyl-1-aza-1.3-butadiene 11 for assemblage of a pyridone 1) ring precursor central to the structure. A Friedlander condensation is utilized for constructing the AB ring system of 1 and 3. An acid-catalyzed reaction sequence is used to accomplish a deprotection with subsequent ring-closure for introduction of the C ring in a single step.

Total synthesis of the cytotoxic alkaloid luotonin A

The structure of luotonin A was unambiguously confirmed by total synthesis. Deprotonation of 3-oxo-1H-pyrrolo[3,4-b]quinoline gave an anion which was coupled with 2-sulfinylaminobenzoyl chloride (prepared by reaction of anthranilic acid with thionyl chlor

2-(2-imidazolin-2-yl)-pyridines and quinolines, process and intermediates for the preparation thereof, and use of said compounds as herbicidal agents

There are provided novel 2-(2-imidazolin-2-yl)pyridine and quinoline compounds, a process and intermediate compounds for the preparation thereof, and a method for controlling a wide variety of annual and perennial plant species therewith.

Process for the preparation of 2,3-quinolinedicarboxylic acids

There is provided a novel process for the preparation of a substituted or unsubstituted 2,3-quinolinedicarboxylic acid, utilizing as the starting material, 2-methyl-3-quinolinecarboxylic acid or 3-methyl-2-quinolinecarboxylic acid or the alkyl ester of either of the above compounds.