2 Quinolineethanol
Quinoline Thiophene Imidazole Thiazole
2-Quinolineethanol
Chemical Formula C11H11NO
Appearance Solid
Odor Odorless
Melting Point 76 - 78 °C
Boiling Point 334.9 °C at 760 mmHg
Density 1.136 g/cm³
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone
Flash Point 156.3 °C
FAQ

What are the physical properties of 2-Quinolineethanol?

2-Quinolineethanol, that is, 2-quinolineethanol, is a kind of organic compound. Its physical properties are quite critical, and the following are described in detail by you.

First of all, its appearance, 2-quinolineethanol is often in the state of white to light yellow crystalline powder, which is easy to observe and distinguish. In many chemical experiments and industrial application scenarios, this appearance feature can help researchers and practitioners to preliminarily judge the properties of substances.

Second, the melting point of this substance is about 137-140 ° C. The melting point is an important physical constant of the substance. By measuring the melting point, the purity of the substance can be checked. If the measured melting point is consistent with the standard value and the melting range is narrow, it indicates that the purity of the substance is quite high; conversely, if the melting range is too wide or the melting point deviates from the standard value, it indicates that it may contain impurities.

In addition, 2-quinoline ethanol also has characteristics in terms of solubility. It is slightly soluble in water, but soluble in common organic solvents such as ethanol and acetone. This solubility characteristic is of great significance in the separation, purification and chemical reaction process of substances. For example, in the chemical synthesis reaction, the selection of an appropriate organic solvent can promote the full dissolution of 2-quinoline ethanol, thereby improving the reaction rate and yield; in the separation process, according to its solubility difference, extraction and other means can be used to achieve effective separation from other substances.

In addition, the density of 2-quinoline ethanol is also a key physical property parameter. Although the exact value needs to be determined according to specific experimental conditions, its density plays a guiding role in solution preparation, reaction system design, etc., and is related to the accurate calculation of the dosage of each substance and the stability of the reaction system.

The physical properties of 2-quinoline ethanol, from appearance, melting point, solubility to density, have an indispensable impact on its research, production and application in the field of chemistry, and play an important role in many fields such as chemical production and drug development.

What are the chemical properties of 2-Quinolineethanol?

2 - Quinolineethanol is an organic compound with unique chemical properties and many interesting properties.

Looking at its structure, it contains a quinoline ring and an ethanol group. The quinoline ring contains nitrogen heterocycles, which are aromatic and have certain stability and electron cloud distribution characteristics. The ethanol group contains hydroxyl groups, which give the compound the typical properties of partial alcohols.

In terms of reactivity, hydroxyl groups can participate in many reactions. If it can be esterified with acids, it can form corresponding esters. Under suitable conditions, it can react with acylating reagents such as acyl halides and acid anhydrides to form ester derivatives. This reaction is often used in organic synthesis to introduce specific functional groups or modify molecular structures.

In addition, hydroxyl groups can also participate in dehydration reactions. If there are appropriate catalysts and reaction conditions, intramolecular dehydration can occur to form olefins, or intermolecular dehydration can occur to form ethers.

Due to the presence of quinoline rings, 2-Quinolineethanol can participate in some reactions involving heterocycles. The nitrogen atom on the quinoline ring has a lone pair of electrons, which can participate in nucleophilic reactions as an electron donor, and can also coordinate with metal ions to form metal complexes. This property may have applications in the field of materials science and catalysis.

At the same time, the reactivity of the compound to some reagents is affected by other parts of the molecule. For example, the substituent on the quinoline ring can change its electron cloud density, which in turn affects the reactivity of hydroxyl groups, or changes the reaction selectivity of the whole molecule to electrophilic and nucleophilic reagents.

In summary, 2-Quinolineethanol has potential applications in organic synthesis, medicinal chemistry and other fields due to its special structure and rich chemical properties.

What are the common uses of 2-Quinolineethanol?

2-Quinoline ethanol is often used for various wonders due to its unique properties. In the field of medicine, it is often a key raw material for the development of pharmaceuticals. Gein 2-quinoline ethanol has a specific chemical structure and activity, and can participate in many pharmacological reactions, helping to create good medicines against diseases. In the field of medicinal chemistry, if it can be precisely formulated, it may be able to develop prescriptions with significant curative effects on specific diseases, adding to the medical way to treat diseases and save people.

In the path of chemical industry, it is also an important chemical raw material. In the field of organic synthesis, it can be used as a key intermediate to construct complex and diverse organic compounds through a series of delicate chemical reactions. The preparation of many fine chemical products relies on the participation of 2-quinoline ethanol, such as special dyes and high-performance additives. With its unique chemical properties, it can give products unique characteristics and improve their quality and performance.

Furthermore, in the road of scientific research, 2-quinoline ethanol is also indispensable. Scientists often use this as a basis to explore new reaction paths and unearth unknown chemical phenomena. Through in-depth study of its chemical properties and reaction mechanism, it may open up new horizons in the field of chemistry, inject new vitality into the development of chemistry, and lead chemical research to a higher peak.

What are the synthesis methods of 2-Quinolineethanol?

The synthesis method of 2-quinoline ethanol has been known in ancient times, and now it is detailed by Jun Chen.

First, quinoline is used as the base, and the nucleophilic substitution method is used. First, quinoline and halogenated ethanol are reacted at co-temperature in suitable bases and solvents. Base agents such as potassium carbonate can promote the departure of the halogen atom of halogenated ethanol, while the nitrogen atom of quinoline is attacked nucleophilically, and then it becomes 2-quinoline ethanol. This reaction needs to be controlled by temperature. If the temperature is too high, side reactions will occur, and if it is too low, the reaction will be delayed.

Second, the method of metal catalysis is used. Transition metal catalysts, such as palladium, are used to catalyze the reaction of quin The metal catalyst can activate the substrate and greatly increase the reaction activity. In this process, aptamers need to be selected to increase the selectivity and activity of the catalyst. The reaction is carried out under the protection of inert gas to prevent the oxidation of the metal catalyst from deactivation.

Third, it is converted from quinoline derivatives. First, quinoline derivatives containing convertible groups, such as quinoline aldehyde or quinoline one, are prepared. Taking quinoline aldehyde as an example, it can be converted into 2-quinoline ethanol through a series of reactions such as reduction and hydroxylation. Strong reducing agents such as lithium aluminum hydride are commonly used in the reduction step, and suitable reagents and conditions are selected for hydroxylation according to specific conditions. < Br >
This number method has its own advantages and disadvantages, and the practical application depends on factors such as raw material availability, cost and reaction conditions.

What are the precautions for the storage and transportation of 2-Quinolineethanol?

2-Quinoline ethanol is also an organic compound. When storing and transporting, it is necessary to pay attention to many matters.

First, it is related to storage. This compound should be placed in a cool, dry and well-ventilated place. If it is in a high temperature and humid environment, its properties may change. High temperature can accelerate its chemical reaction, and humid gas can also cause adverse reactions such as hydrolysis, which will damage its quality. And it should be kept away from fire and heat sources to prevent it from being dangerous due to heat. It must be stored separately from oxidizing agents and acids, and must not be mixed. If these substances come into contact with it, it is easy to cause violent reactions and endanger safety.

Second, as for transportation. Make sure the packaging is complete and sealed before transportation. If the package is damaged, 2-quinoline ethanol or leakage will not only pollute the environment, but also easily cause personal contact and injury. During transportation, the speed should be stable, and violent shaking such as sudden braking and sharp turns should be avoided to prevent the package from crashing and breaking. Transportation vehicles also need to be equipped with corresponding varieties and quantities of fire-fighting equipment and leakage emergency treatment equipment for emergencies. Escort personnel must be familiar with the characteristics and emergency treatment methods of 2-quinoline ethanol, and closely monitor during transportation. If there is any abnormality, they should be properly disposed of immediately. In this way, Fang Guaranteed 2-quinoline ethanol is safe during storage and transportation.