2 Chloroquinoline
Quinoline Thiophene Imidazole Thiazole
2-Chloroquinoline
Chemical Formula C9H6ClN
Molar Mass 163.604 g/mol
Appearance Yellow - brown solid
Melting Point 49 - 52 °C
Boiling Point 265 - 266 °C
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, chloroform
Flash Point 112.8 °C
FAQ

What are the physical properties of 2-Chloroquinoline?

2-Chloroquinoline is also an organic compound. Its physical properties can be quite studied.

Looking at its properties, it is mostly white to light yellow crystalline powder under normal conditions. This color and state are its intuitive signs, and it is visible to the eye.

When it comes to the melting point, it is about 68-72 ° C. For the melting point, the critical temperature for the substance to change from solid to liquid is also. When the ambient temperature rises to S value, 2-chloroquinoline melts from solid to liquid. This property is an important guide in the purification, identification and related chemical processes of the substance.

As for the boiling point, it is about 305 ° C. Boiling point, the temperature at which the vapor pressure of a liquid is equal to the external atmospheric pressure. At this boiling point, 2-chloroquinoline converts from a liquid state to a gaseous state. This value is related to its physical state transition in a high temperature environment. It is a key parameter in chemical distillation, separation and other operations.

Solubility is also an important physical property. 2-chloroquinoline is slightly soluble in water, but it has good solubility in organic solvents such as ethanol, ether, and chloroform. This property makes it participate in many chemical reactions using organic solvents as a medium, and can be effectively operated in the process of extraction, separation, and preparation of substances due to its difference in solubility. < Br >
In terms of density, although the specific value may vary depending on the measurement conditions, it is roughly within a certain range. Density, the mass per unit volume of a substance, is related to its distribution and behavior in different media. In practical application scenarios such as chemical pipeline transportation and storage container design, it is an indispensable consideration.

In addition, 2-chloroquinoline has a certain volatility. Although the volatility is not very strong, under specific environments and conditions, its volatility cannot be ignored, or it has an impact on the environment and operation process.

In light of the above physical properties, it is fundamental and critical information in many fields such as chemical synthesis, drug research and development, material preparation, etc., which helps all kinds of research and applications to understand their properties and make good use of them.

What are the chemical properties of 2-Chloroquinoline?

2-Chloroquinoline is an organic compound with unique chemical properties and many important characteristics. This is a detailed description for you.

First of all, 2-chloroquinoline contains chlorine atoms, which make it have a certain nucleophilic substitution activity. The chlorine atom can be replaced by a variety of nucleophilic reagents. Because the chlorine atom is a good leaving group, it can react with nucleophilic reagents under suitable conditions. For example, in an alkaline environment, nucleophilic reagents such as hydroxyl negative ions can attack the carbon atoms attached to the chlorine atom of 2-chloroquinoline, causing nucleophilic substitution, and the chlorine atoms leave to form corresponding hydroxyl-containing derivatives. This reaction is an important way to prepare compounds such as 2-quinolinol.

Secondly, the quinoline ring of 2-chloroquinoline is aromatic, which gives it certain stability and special electronic properties. The conjugate system of the quinoline ring makes the electron cloud uniformly distributed and not easy to be oxidized or added. However, under specific strong oxidants or special conditions, the quinoline ring can also react. For example, under strong oxidation conditions, some groups on the quinoline ring may be oxidized to form oxygen-containing compounds.

Furthermore, the nitrogen atom of 2-chloroquinoline has a certain alkalinity. The lone pair electron on the nitrogen atom can accept protons, and in acidic solutions, it can combine with protons to form salts. This alkalinity makes it possible to neutralize and react with acids to form corresponding salts, and the solubility of this salt in water may be different from that of 2-chloroquinoline ontology, which can be used to separate and purify 2-chloroquinoline.

In addition, 2-chloroquinoline can participate in some metal catalytic reactions. For example, under the catalysis of transition metals, it can be coupled with organoboronic acids and other reagents to form carbon-carbon bonds or carbon-heteroatomic bonds. This is an important means of constructing complex organic molecules and is widely used in drug synthesis, materials science and other fields. The chemical properties of 2-chloroquinoline are rich and diverse, including nucleophilic substitution, aromaticity, alkalinity, and metal-catalyzed reactions, which make it play a key role in many fields such as organic synthesis and drug development, and provide an important foundation for chemical research and industrial production.

What is the common synthesis method of 2-Chloroquinoline?

2-Chloroquinoline is also an organic compound, and is widely used in the fields of medicine, pesticides and materials. The common synthesis methods generally include the following:

First, the method of using quinoline as the starting material. Quinoline is chlorinated to obtain 2-chloroquinoline. This chlorination method has different paths. If chlorine is used as a chlorination agent, under the presence of appropriate temperature, pressure and catalyst, chlorine gas reacts with quinoline, and chlorine atoms replace hydrogen atoms at the 2-position of quinoline to form 2-chloroquinoline. However, this method needs to pay attention to the control of the reaction conditions. Too high or too low temperature, improper amount of chlorine gas, etc., may cause side reactions to occur, forming other chloroquinoline isomers or deep chlorinated products, which affect the purity and yield of the products.

Second, the quinoline ring is formed by the reaction of aniline compounds with halogenated hydrocarbons, and then 2-chloroquinoline is synthesized. First, aniline and suitable halogenated hydrocarbons are reacted under the action of bases to form an intermediate product, and then the intermediate product is cyclized to form a quinoline ring. If a chlorine-containing group is ingeniously introduced in the reaction design, it can be directly or through subsequent reactions converted to 2-chloroquinoline. This path requires careful design of reaction steps and conditions to ensure the smooth progress of each step of the reaction. It is also crucial for the purification and identification of the reaction intermediates to ensure the structure and purity of the final product.

Third, the synthesis method based on the Skraup reaction. The Skraup reaction usually uses aniline, glycerol, concentrated sulfuric acid and oxidants (such as nitrobenzene, etc.) as raw materials to generate quinoline derivatives through complex reaction processes. If in the reaction system, appropriate adjustment of the raw material structure or reaction conditions can make the reaction tend to introduce chlorine atoms at the 2-position to obtain 2-chloroquinoline. However, this reaction is more intense, the reaction temperature and feeding sequence need to be strictly controlled to prevent danger, and the post-reaction treatment is also more cumbersome, and a variety of separation and purification methods are required to obtain high-purity 2-chloroquinoline.

The above synthesis methods have their own advantages and disadvantages. In practical applications, the most suitable synthesis path should be selected according to specific needs, considering the availability of raw materials, cost, difficulty of reaction conditions, product purity and yield, etc.

2-Chloroquinoline is used in what fields

2-Chloroquinoline has its uses in various fields. In the field of medicine, it can be used as a raw material for the creation of antimalarial drugs. Malaria is a disease that seriously endangers human health. Plasmodium parasites are rampant, causing fever, chills, headaches and other diseases. In the past, malaria epidemics were rampant, and people were struggling. The antimalarial drugs made of 2-chloroquinoline are like a god's weapon, which can effectively kill malaria parasites and relieve people's suffering.

In the field of pesticides, 2-chloroquinoline also has important functions. It can be used to prepare anti-insect and insecticidal agents. Field crops are often devoured by pests, resulting in a sharp decrease in harvest. The pesticide made of 2-chloroquinoline can prevent pests from attacking and keep crops flourishing, just like the soldiers of ancient times, protecting the peace of the pasture.

Furthermore, in the realm of material chemistry, 2-chloroquinoline can participate in the synthesis of special materials. Special materials, widely used, or used in aerospace, or electronic equipment. With its synthetic materials, or with special physical and chemical properties, it can help the progress of science and technology, just like a skilled craftsman making strange tools from good materials.

In addition, in the field of organic synthetic chemistry, 2-chloroquinoline is an important intermediate. Organic synthesis aims to create various organic compounds. 2-chloroquinoline can be converted into complex organic molecules through various chemical reactions, such as the cornerstone of building tall buildings, laying the foundation for the great cause of organic synthesis.

What is the production process of 2-Chloroquinoline?

2-Chloroquinoline is also an organic compound. The method of its preparation, in the past, craftsmen used to follow various paths to make it.

One method, using quinoline as the starting material, obtained by chlorination. Quinoline is placed in the kettle, and an appropriate chlorinating agent, such as chlorine gas or a chlorine-containing reagent, is added. Heat and control its temperature, so that the two are combined. This process must strictly monitor the reaction state to ensure the purity of the product. Due to the structure of quinoline, the chlorination position is selected. To obtain 2-chloroquinoline, the conditions must be well controlled, and the chlorine atom is just at the two position.

Another method, based on other organic compounds, is caused by multiple steps. First, a substrate with a suitable structure is taken, and after several reactions, the structure gradually becomes quinoline-like, and chlorine atoms are introduced into the binary position at an appropriate time. Although this method is complicated, it can obtain higher yield and purity under specific circumstances.

When preparing, it also concerns various details. For example, the choice of solvent, different solvents have an impact on the speed of reaction and the shape of the product. And the temperature and time of the reaction are also important factors. High temperature will cause the reaction speed, and then it may cause the production of side effects; although it may increase the yield over time, it will take time. Therefore, in order to make 2-chloroquinoline well, craftsmen must be familiar with all factors and fine-tune the process, so as to achieve both quality and quantity.