2-Methyl-5-Aminoquinoline

2-Methyl-5-aminoquinoline is one of the organic compounds. It has a wide range of uses and has important applications in many fields.
Bearing the brunt, in the field of pharmaceutical chemistry, 2-methyl-5-aminoquinoline is often used as a key intermediate. The synthesis of many drugs relies on its participation to build a specific chemical structure, which in turn endows the drug with unique pharmacological activity. Due to its structural properties, it can be chemically modified to interact with specific targets in organisms, paving the way for the development of new drugs. For example, in the process of creating some antimicrobial and anticancer drugs, 2-methyl-5-aminoquinoline is used as a starting material or key structural unit, and is converted into a therapeutic drug molecule through a multi-step reaction.
Furthermore, in the field of materials science, this compound has also emerged. It can be used to prepare functional materials, such as organic optoelectronic materials. Because its molecular structure can absorb and emit light of specific wavelengths, it can be applied to the manufacture of devices such as organic Light Emitting Diodes (OLEDs) and solar cells. In OLEDs, it can be used as a light-emitting layer material to endow the device with good luminous properties; in solar cells, it can help improve the photoelectric conversion efficiency.
In addition, 2-methyl-5-aminoquinoline is also useful in the field of analytical chemistry. It can be used as an analytical reagent for the detection and quantitative analysis of specific substances. Because of its specific recognition ability for certain ions or compounds, accurate detection of the target is achieved through chemical reactions or spectral changes. For example, in the detection of certain metal ions, specific complexes are formed with them, causing color or fluorescence changes, so that the presence and content of metal ions can be easily detected.
To sum up, 2-methyl-5-aminoquinoline plays an indispensable role in many fields such as medicinal chemistry, materials science and analytical chemistry, and is of great significance to promote the development of related fields.

2-Methyl-5-aminoquinoline is also an organic compound. Its physical properties are quite impressive.
Looking at its properties, it is mostly solid at room temperature. This is due to the force between molecules, so that it can maintain a solid state in common temperature environments. As for the color, it is often white to light yellow, like a yellowish book of years precipitation, simple but elegant.
When it comes to the melting point, it is about a specific temperature range. This temperature value is crucial for identifying and purifying the compound. Because the melting point is one of the inherent characteristics of the substance, accurate determination of the melting point can determine the purity of its quality. When heated to the melting point, 2-methyl-5-aminoquinoline gradually melts from a solid state to a liquid state, just like ice and snow in warm spring, quietly changing its form.
Furthermore, its solubility is also a key property. In organic solvents, such as ethanol and chloroform, it exhibits a certain solubility. Due to the principle of similarity and compatibility, there is a suitable interaction between the molecular structure of the compound and the molecules of the organic solvent, so it is soluble. However, in water, the solubility is relatively limited, which is due to the difference between the polarity of water and the molecular polarity of the compound.
In addition, the density of 2-methyl-5-aminoquinoline also has its unique value. The density of the compound reflects the degree of compactness of its internal structure, which is related to its behavior when mixed with other substances in practical applications.
As for its volatility, it is relatively low. Due to the strong intermolecular force, the molecule is not easy to break free and escape into the gas phase, which makes the compound exist relatively stably under conventional conditions, and is not easy to be lost due to volatilization. These many physical properties are indispensable in many fields such as chemical research and drug synthesis, providing guidance for exploring the secrets of the compound.

The synthesis of 2-methyl-5-aminoquinoline has been known for a long time and has various methods. First, it can be started by nitrogen-containing heterocyclic compounds. Take appropriate pyridine derivatives, and through ingenious reaction steps, such as under specific reaction conditions and catalyzed by suitable catalysts, the pyridine ring and the benzene ring are ingeniously connected to construct a quinoline skeleton. In this process, precise control of the reaction temperature, pressure and proportion of reactants is required to ensure the smooth progress of the reaction and improve the yield of the target product.
Furthermore, using aniline compounds as raw materials is also a commonly used method. The aniline derivative and the appropriate aldehyde compound in a specific solvent, under the catalytic action of acid or base, first condensation reaction occurs to form an intermediate product. Subsequently, through further cyclization reaction, the quinoline structure is formed. This path needs to pay attention to the selectivity of the reaction to avoid unnecessary by-products and affect the purity of the product.
Another method of modifying the quinoline parent compound is based on the quinoline. Quinoline is obtained first, and then its specific position is methylated and aminated. When methylating, select a suitable methylating agent, such as iodomethane, and introduce methyl under suitable reaction conditions. In the amination step, ammonolysis and other methods can be used to introduce amino groups at the 5-position. This process requires high control of the reaction conditions to achieve precise chemical modification.
All synthetic methods have their own advantages and disadvantages, and they need to be carefully selected according to the actual experimental conditions, the availability of raw materials, and the purity requirements of the target product.

2-Methyl-5-aminoquinoline is in the market, and its price range is difficult to determine. The price of this compound often varies due to various factors.
First, the amount is involved. If the purchase is huge, the merchant may make a profit, with small profits but quick turnover, the unit price may drop; if only a small amount is needed for research and testing, etc., the unit price may be high.
Second, the source is different. Those from different manufacturers have different prices. Famous works and high-quality factories produce prices that may be too high; however, factories that are initially involved in this field and want to expand the city may compete for customers, and the price may be close to the people.
Third, the change of times. The state of market supply and demand, the fluctuation of the amount of raw materials and the price can cause its price to fluctuate. There are many in demand, but the supply is limited, and the price may rise; otherwise, the price may be depressed.
According to the "Tiangong Kaiwu", although there is no price of this specific product, it is also possible to discuss the production system and circulation of the product. Therefore, in order to know the price of 2-methyl-5-aminoquinoline, when consulting the reagent merchants, or checking the latest price information of the chemical raw material trading platform, you can get a more accurate price range.

2-Methyl-5-aminoquinoline is one of the organic compounds. Its storage is essential to the stability and long-term survival of this substance, as well as the safety and efficacy of the experiment.
If you want to store 2-methyl-5-aminoquinoline well, the first choice is the environment. When placed in a cool place, avoid direct sunlight. Sunlight can make the compound photochemical reaction, or cause decomposition and deterioration. A cool place with constant and low temperature can slow down the rate of its chemical reaction and maintain its chemical stability.
Second, a dry environment is also essential. 2-Methyl-5-aminoquinoline is sensitive to moisture, if moisture enters, or causes reactions such as hydrolysis. Therefore, the storage device should be tightly sealed to prevent moisture from invading. It can be used in glass bottles or plastic bottles. The mouth seal method, or the screw cap is tightly closed, or the wax seal is used to ensure that the air is tight.
Furthermore, it is important to store this compound away from sources of fire and oxidants. 2-Methyl-5-aminoquinoline is flammable, and it will burn in case of fire, or even cause explosion, endangering safety. Oxidants can also react violently with it, damaging its quality. Therefore, when storing, it is appropriate to store it in separate compartments away from the fire source and oxidant.
In addition, the label should not be ignored. On the reservoir, the name of "2-methyl-5-aminoquinoline" should be marked in detail, and letters such as chemical formula and danger warning should be attached. In this way, when using it, it is clear at a glance, which can avoid the risk of misuse and ensure the safety of the experiment and the user.
In short, to properly store 2-methyl-5-aminoquinoline, it is necessary to choose a cool and dry place, seal its container, and keep it away from the fire source and oxidant, and explain its label. Only by having both of these can we achieve the purpose of stability and ensure its quality and safety for scientific research and production.