• 1. Formula index
  J. Chem. Soc. 1933 1686
• 2. Organic chemistry
  J. Chem. Soc. Abstr. 1925 128 i349

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Quinolines and derivatives Quinolones and derivatives

2-Methoxy-4-methylquinoline (CAS No. 15113-00-5)

2-Methoxy-4-methylquinoline is a heterocyclic organic compound with the CAS registry number 15113-00-5. This compound belongs to the quinoline family, which is a bicyclic structure consisting of a benzene ring fused to a pyridine ring. The presence of a methoxy group at the 2-position and a methyl group at the 4-position introduces unique chemical properties and functional groups that make this compound interesting for various applications in chemistry and materials science.

The synthesis of 2-Methoxy-4-methylquinoline typically involves multi-step organic reactions, often utilizing substitution or condensation mechanisms. Recent advancements in synthetic methodologies have enabled more efficient and selective routes to prepare this compound, reducing production costs and minimizing environmental impact. For instance, researchers have explored the use of microwave-assisted synthesis and catalytic systems to enhance reaction yields and purity levels.

One of the most notable applications of 2-Methoxy-4-methylquinoline is in the field of drug discovery. The compound has been studied for its potential as a lead molecule in the development of new pharmaceutical agents. Its structure provides a scaffold for further functionalization, allowing chemists to explore its pharmacokinetic properties and bioavailability. Recent studies have highlighted its ability to interact with specific biological targets, such as enzymes or receptors, making it a promising candidate for therapeutic interventions.

In addition to its role in pharmacology, 2-Methoxy-4-methylquinoline has found applications in materials science. The compound's aromaticity and conjugated system contribute to its electronic properties, which are valuable in the design of organic semiconductors and optoelectronic devices. Researchers have investigated its use in organic light-emitting diodes (OLEDs) and photovoltaic cells, where its ability to absorb and emit light at specific wavelengths is advantageous.

The chemical stability of 2-Methoxy-4-methylquinoline under various conditions has also been a subject of recent research. Studies have shown that the compound exhibits good thermal stability and resistance to oxidation, making it suitable for high-temperature applications. However, its reactivity towards certain chemical reagents, such as strong acids or bases, has been documented, highlighting the need for careful handling during synthesis and processing.

From an environmental perspective, understanding the fate and transport of 2-Methoxy-4-methylquinoline in natural systems is crucial. Recent ecological studies have assessed its biodegradability and potential toxicity to aquatic organisms. These findings are essential for regulating its use and ensuring sustainable practices in industries that utilize this compound.

In conclusion, 2-Methoxy-4-methylquinoline (CAS No. 15113-00-5) is a versatile compound with a wide range of applications across multiple disciplines. Its unique chemical structure, coupled with recent advancements in synthesis and application development, positions it as an important material for future innovations in medicine, electronics, and beyond.

• 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
• 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
• 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
• 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)
• 89640-58-4(2-Iodo-4-nitrophenylhydrazine)
• 1449132-38-0(3-Fluoro-5-(2-fluoro-5-methylbenzylcarbamoyl)benzeneboronic acid)
• 2034271-14-0(2-(1H-indol-3-yl)-N-{[6-(thiophen-2-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl]methyl}acetamide)