Description

6-Fluoro-3-Methyl-2-Phenylquinoline-4-Carboxylic Acid is a high-purity, advanced pharmaceutical intermediate with a defined quinoline core structure. This compound is valued for its role as a critical building block in the synthesis of novel active pharmaceutical ingredients (APIs), particularly in therapeutic areas requiring complex heterocyclic frameworks. It is essential for research and development chemists and manufacturers in the global pharmaceutical, agrochemical, and advanced materials sectors seeking reliable, high-quality intermediates for complex synthesis.

Application

• Pharmaceutical Intermediate: A key precursor in the synthesis of novel drug candidates, especially those targeting central nervous system (CNS) disorders, anti-infectives, and oncology.
• Agrochemical Research: Serves as a building block for developing new generation herbicides, fungicides, and pesticides with enhanced efficacy.
• Material Science: Used in the research and development of organic light-emitting diodes (OLEDs) and other advanced electronic materials due to its fluorinated quinoline structure.
• Chemical Synthesis: Employed in academic and industrial R&D for constructing complex heterocyclic compounds and exploring new reaction pathways.
• Ligand & Catalyst Development: Acts as a precursor for creating specialized ligands used in catalytic processes and metal-organic frameworks (MOFs).

Basic Information

Product Name	6-Fluoro-3-Methyl-2-Phenylquinoline-4-Carboxylic Acid
CAS No.	130507-38-9
Molecular Formula	C18H12FNO2
Molecular Weight	293.29 g/mol
Synonyms	6-Fluoro-3-methyl-2-phenyl-4-quinolinecarboxylic acid; 2-Phenyl-6-fluoro-3-methylquinoline-4-carboxylic acid; 4-Quinolinecarboxylic acid, 6-fluoro-3-methyl-2-phenyl-; 130507-38-9; 6-Fluoro-3-methyl-2-phenylquinoline-4-carboxylate; 6-Fluoro-3-methyl-2-phenyl-4-quinolinecarboxylate
EINECS	Contact for details

Quality Control

Every batch of 6-Fluoro-3-Methyl-2-Phenylquinoline-4-Carboxylic Acid is manufactured under strict quality management systems. Our products undergo rigorous analytical testing, including HPLC, NMR, and MS, to ensure identity, purity, and consistency meet the high standards required for pharmaceutical R&D and production. A comprehensive Certificate of Analysis (COA) detailing all specifications is provided with each shipment and is available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and light-sensitive; containers must be kept tightly sealed and away from direct light sources to maintain stability and purity.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Conforms to reference standard
Assay (HPLC)	≥ 98.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 10 ppm
Related Substances (HPLC)	Individual impurity ≤ 0.5%; Total impurities ≤ 1.0%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.