Linshang Chemical
PRODUCTS
2,3,5,6-Tetrachloromethoxybenzene
Linshang Chemical
|
HS Code |
492857 |
| Chemical Formula | C7H2Cl4O |
| Molar Mass | 259.903 g/mol |
| Appearance | Solid |
| Solubility In Water | Insoluble |
As an accredited 2,3,5,6-Tetrachloromethoxybenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 2,3,5,6 - tetrachloromethoxybenzene packaged in a sealed plastic container. |
| Storage | 2,3,5,6 - tetrachloromethoxybenzene should be stored in a cool, dry, well - ventilated area. Keep it away from sources of ignition and heat. Store in a tightly closed container, preferably made of a material resistant to chemical corrosion, such as glass or certain plastics. Separate it from incompatible substances to prevent potential reactions. |
| Shipping | 2,3,5,6 - tetrachloromethoxybenzene is shipped in sealed, corrosion - resistant containers. It follows strict hazardous chemical shipping regulations, with proper labeling and documentation to ensure safe transportation. |
Competitive 2,3,5,6-Tetrachloromethoxybenzene prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615365006308 or mail to info@alchemist-chem.com.
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Tel: +8615365006308
Email: info@alchemist-chem.com
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As a leading 2,3,5,6-Tetrachloromethoxybenzene supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
What is the use of 2,3,5,6-tetrachloromethoxybenzene?
2% 2C3% 2C5% 2C6-tetrafluoroethoxyphenyl This substance is useful in various applications. It is quite useful in the field of pharmaceutical chemistry.
In the process of pharmaceutical creation, 2% 2C3% 2C5% 2C6-tetrafluoroethoxyphenyl is often the key raw material. Based on it, a variety of specific drugs can be prepared. Due to its unique chemical structure, it can precisely fit with specific targets in the body, thus helping the drug to exert an efficient therapeutic effect. For example, in the synthesis of some antiviral drugs, the introduction of this group can greatly enhance the drug's ability to inhibit viruses, improve the efficacy of drugs, and bring good news to patients.
In the field of materials science, 2% 2C3% 2C5% 2C6-tetrafluoroethoxy phenyl also has extraordinary performance. Adding this ingredient to polymer materials can significantly improve the properties of materials. It can enhance the heat resistance of materials, so that materials can maintain stable structures and properties in high temperature environments without deformation or damage. At the same time, it can also improve the chemical stability of materials, make materials more resistant to chemical corrosion, prolong the service life of materials, and have broad application prospects in fields such as aerospace, electronics and electrical appliances that require strict material properties.
In the field of pesticide research and development, 2% 2C3% 2C5% 2C6-tetrafluoroethoxy phenyl also plays an important role. The pesticide developed on this basis has a high-efficiency killing effect on pests and is less harmful to the environment. It can precisely act on the physiological system of pests and interfere with the normal growth and reproduction of pests, so as to achieve good insecticidal effect, while reducing the negative impact on the ecological environment. It is in line with the current development concept of green environmental protection.
All in all, 2% 2C3% 2C5% 2C6-tetrafluoroethoxybenzene is based on medicine, materials, pesticides and many other fields. With its unique chemical properties, it plays an indispensable role in promoting technological progress and development in various fields.
In the process of pharmaceutical creation, 2% 2C3% 2C5% 2C6-tetrafluoroethoxyphenyl is often the key raw material. Based on it, a variety of specific drugs can be prepared. Due to its unique chemical structure, it can precisely fit with specific targets in the body, thus helping the drug to exert an efficient therapeutic effect. For example, in the synthesis of some antiviral drugs, the introduction of this group can greatly enhance the drug's ability to inhibit viruses, improve the efficacy of drugs, and bring good news to patients.
In the field of materials science, 2% 2C3% 2C5% 2C6-tetrafluoroethoxy phenyl also has extraordinary performance. Adding this ingredient to polymer materials can significantly improve the properties of materials. It can enhance the heat resistance of materials, so that materials can maintain stable structures and properties in high temperature environments without deformation or damage. At the same time, it can also improve the chemical stability of materials, make materials more resistant to chemical corrosion, prolong the service life of materials, and have broad application prospects in fields such as aerospace, electronics and electrical appliances that require strict material properties.
In the field of pesticide research and development, 2% 2C3% 2C5% 2C6-tetrafluoroethoxy phenyl also plays an important role. The pesticide developed on this basis has a high-efficiency killing effect on pests and is less harmful to the environment. It can precisely act on the physiological system of pests and interfere with the normal growth and reproduction of pests, so as to achieve good insecticidal effect, while reducing the negative impact on the ecological environment. It is in line with the current development concept of green environmental protection.
All in all, 2% 2C3% 2C5% 2C6-tetrafluoroethoxybenzene is based on medicine, materials, pesticides and many other fields. With its unique chemical properties, it plays an indispensable role in promoting technological progress and development in various fields.
What are the physical properties of 2,3,5,6-tetrachloromethoxybenzene?
2% 2C3% 2C5% 2C6 -tetrafluoroethoxy phenyl, which is an organic compound or the like. Its physical properties are quite specific and have various characteristics, as detailed below:
First of all, its properties, at room temperature, this substance may be in a liquid state, the texture is mostly clear and has a certain fluidity. It is similar to clear water, but its chemical composition endows it with special properties that are far from comparable to clear water.
The boiling point is discussed, and its boiling point is within a specific range due to the force between molecules. Generally speaking, compared with common simple organic compounds, because of its fluorine atom, fluorine has extremely high electronegativity, which increases the intermolecular force, so the boiling point is higher. This property makes it occur in a specific temperature environment. Phase transition, from liquid to gas.
Melting point also has unique features. Due to the regularity of molecular structure and the interaction between atoms, its melting point or relatively stable. The specific lattice structure and the attractive force between molecules determine that it requires specific temperature conditions, the lattice begins to be destroyed, and the substance changes from solid to liquid.
In terms of solubility, this substance has good solubility in organic solvents. Due to the fact that its molecular structure contains organic groups such as phenyl groups, it has a similar chemical structure to organic solvents. According to the principle of "similar miscibility", it is easily soluble in organic solvents such as toluene and dichloromethane. However, its solubility in water is poor. Because water is a polar molecule, and the polarity of the substance is relatively weak, the force between the two molecules is difficult to achieve the degree of mutual dissolution.
The density is slightly higher than that of common organic solvents. This is because the fluorine atom has a relatively large atomic weight and a tight molecular structure, resulting in an increase in the mass of the substance per unit volume, so the density increases.
In addition, the substance may have a certain volatility. Although the volatility is not as strong as that of small molecule organic solvents due to intermolecular forces, it will still evaporate slowly in the air under specific temperature, ventilation and other conditions.
In summary, 2% 2C3% 2C5% 2C6 -tetrafluoroethoxy phenyl has unique physical properties and has important application value in many fields such as organic synthesis and materials science. Its special properties can endow materials with specific functions and provide an important material basis for the development of related fields.
First of all, its properties, at room temperature, this substance may be in a liquid state, the texture is mostly clear and has a certain fluidity. It is similar to clear water, but its chemical composition endows it with special properties that are far from comparable to clear water.
The boiling point is discussed, and its boiling point is within a specific range due to the force between molecules. Generally speaking, compared with common simple organic compounds, because of its fluorine atom, fluorine has extremely high electronegativity, which increases the intermolecular force, so the boiling point is higher. This property makes it occur in a specific temperature environment. Phase transition, from liquid to gas.
Melting point also has unique features. Due to the regularity of molecular structure and the interaction between atoms, its melting point or relatively stable. The specific lattice structure and the attractive force between molecules determine that it requires specific temperature conditions, the lattice begins to be destroyed, and the substance changes from solid to liquid.
In terms of solubility, this substance has good solubility in organic solvents. Due to the fact that its molecular structure contains organic groups such as phenyl groups, it has a similar chemical structure to organic solvents. According to the principle of "similar miscibility", it is easily soluble in organic solvents such as toluene and dichloromethane. However, its solubility in water is poor. Because water is a polar molecule, and the polarity of the substance is relatively weak, the force between the two molecules is difficult to achieve the degree of mutual dissolution.
The density is slightly higher than that of common organic solvents. This is because the fluorine atom has a relatively large atomic weight and a tight molecular structure, resulting in an increase in the mass of the substance per unit volume, so the density increases.
In addition, the substance may have a certain volatility. Although the volatility is not as strong as that of small molecule organic solvents due to intermolecular forces, it will still evaporate slowly in the air under specific temperature, ventilation and other conditions.
In summary, 2% 2C3% 2C5% 2C6 -tetrafluoroethoxy phenyl has unique physical properties and has important application value in many fields such as organic synthesis and materials science. Its special properties can endow materials with specific functions and provide an important material basis for the development of related fields.
What are the chemical properties of 2,3,5,6-tetrachloromethoxybenzene?
2% 2C3% 2C5% 2C6-tetrafluoroethoxyphenyl, its chemical properties are particularly important. This substance has unique properties and is used in various fields.
Looking at its chemical properties, it has high stability. Due to the fluorine atom, fluorine has strong electronegativity, resulting in a large C-F bond energy, making the substance not easy to be broken by ordinary chemical reagents, and can also maintain stability in the environment of high temperature, strong acid and strong base. This stability makes it suitable for use in special environments, such as in some industrial processes that require resistance to harsh chemical conditions.
Furthermore, it has certain lipophilic properties. The structure of the phenyl group gives it lipophilicity, which is of great significance in the field of medicine. If the drug molecule has lipophilicity, it is easier to penetrate the biofilm, reach the target of action, and improve the drug efficacy. Therefore, 2% 2C3% 2C5% 2C6-tetrafluoroethoxy phenyl can be used as an intermediate for drug synthesis, and its lipophilicity can improve the bioavailability of drugs.
In addition, the substance may have a specific electronic effect. The presence of fluorine atoms affects the electron cloud distribution of the molecule, changing its reactivity and selectivity. In organic synthesis reactions, this electronic effect can guide the reaction in a specific direction, synthesizing compounds with special structures and functions, providing unique raw materials for materials science, fine chemistry and other fields.
Overall, 2% 2C3% 2C5% 2C6-tetrafluoroethoxy phenyl has broad application prospects in many fields such as chemical engineering, medicine, and materials due to its chemical properties such as stability, lipophilicity, and special electronic effects. It needs to be further explored and explored by researchers.
Looking at its chemical properties, it has high stability. Due to the fluorine atom, fluorine has strong electronegativity, resulting in a large C-F bond energy, making the substance not easy to be broken by ordinary chemical reagents, and can also maintain stability in the environment of high temperature, strong acid and strong base. This stability makes it suitable for use in special environments, such as in some industrial processes that require resistance to harsh chemical conditions.
Furthermore, it has certain lipophilic properties. The structure of the phenyl group gives it lipophilicity, which is of great significance in the field of medicine. If the drug molecule has lipophilicity, it is easier to penetrate the biofilm, reach the target of action, and improve the drug efficacy. Therefore, 2% 2C3% 2C5% 2C6-tetrafluoroethoxy phenyl can be used as an intermediate for drug synthesis, and its lipophilicity can improve the bioavailability of drugs.
In addition, the substance may have a specific electronic effect. The presence of fluorine atoms affects the electron cloud distribution of the molecule, changing its reactivity and selectivity. In organic synthesis reactions, this electronic effect can guide the reaction in a specific direction, synthesizing compounds with special structures and functions, providing unique raw materials for materials science, fine chemistry and other fields.
Overall, 2% 2C3% 2C5% 2C6-tetrafluoroethoxy phenyl has broad application prospects in many fields such as chemical engineering, medicine, and materials due to its chemical properties such as stability, lipophilicity, and special electronic effects. It needs to be further explored and explored by researchers.
What is the synthesis method of 2,3,5,6-tetrachloromethoxybenzene?
The synthesis of 2% 2C3% 2C5% 2C6-tetrafluoroethoxy phenyl is an important topic in organic synthetic chemistry. The synthesis method needs to be strictly based on chemical principles and steps.
To synthesize this compound, the common starting materials are benzene ring compounds with appropriate substituents and reagents containing tetrafluoroethoxy groups. The initial step, or the substitution reaction of benzene ring. Benzene and halogenated hydrocarbons can be alkylated by Fu-g under the catalysis of Lewis acid, and suitable alkyl substituents can be introduced to lay the foundation for subsequent reactions.
Then, the obtained alkylbenzene compound is introduced into halogen atoms at specific positions in the benzene ring by halogenation reaction. This halogen atom will play a key role in the subsequent reaction and can be an activity check point for nucleophilic substitution reactions.
At the same time, reagents containing tetrafluoroethoxy are prepared. Usually, tetrafluoroethanol can be reacted with appropriate halogenated hydrocarbons under alkaline conditions to form tetrafluoroethoxy halides. This halogen has good electrophilicity and can undergo nucleophilic substitution reactions with previously prepared halobenzene-containing compounds.
In the nucleophilic substitution stage, the halobenzene-containing compound is mixed with the tetrafluoroethoxy halide, and an appropriate base is added to promote the reaction. The base neutralizes the hydrogen halide generated by the reaction and pushes the reaction equilibrium towards the product direction. During the reaction process, the reaction temperature, time and ratio of reactants need to be precisely controlled to ensure that the reaction is efficient and selective to generate the target product 2% 2C3% 2C5% 2C6-tetrafluoroethoxy phenyl.
After the reaction is completed, the product needs to be separated and purified. Extraction, distillation, column chromatography and other means can be used to remove the residual raw materials, by-products and catalysts in the reaction system to obtain a pure target compound. After this series of steps, 2% 2C3% 2C5% 2C6-tetrafluoroethoxy phenyl can be obtained.
To synthesize this compound, the common starting materials are benzene ring compounds with appropriate substituents and reagents containing tetrafluoroethoxy groups. The initial step, or the substitution reaction of benzene ring. Benzene and halogenated hydrocarbons can be alkylated by Fu-g under the catalysis of Lewis acid, and suitable alkyl substituents can be introduced to lay the foundation for subsequent reactions.
Then, the obtained alkylbenzene compound is introduced into halogen atoms at specific positions in the benzene ring by halogenation reaction. This halogen atom will play a key role in the subsequent reaction and can be an activity check point for nucleophilic substitution reactions.
At the same time, reagents containing tetrafluoroethoxy are prepared. Usually, tetrafluoroethanol can be reacted with appropriate halogenated hydrocarbons under alkaline conditions to form tetrafluoroethoxy halides. This halogen has good electrophilicity and can undergo nucleophilic substitution reactions with previously prepared halobenzene-containing compounds.
In the nucleophilic substitution stage, the halobenzene-containing compound is mixed with the tetrafluoroethoxy halide, and an appropriate base is added to promote the reaction. The base neutralizes the hydrogen halide generated by the reaction and pushes the reaction equilibrium towards the product direction. During the reaction process, the reaction temperature, time and ratio of reactants need to be precisely controlled to ensure that the reaction is efficient and selective to generate the target product 2% 2C3% 2C5% 2C6-tetrafluoroethoxy phenyl.
After the reaction is completed, the product needs to be separated and purified. Extraction, distillation, column chromatography and other means can be used to remove the residual raw materials, by-products and catalysts in the reaction system to obtain a pure target compound. After this series of steps, 2% 2C3% 2C5% 2C6-tetrafluoroethoxy phenyl can be obtained.
What are the precautions for using 2,3,5,6-tetrachloromethoxybenzene?
2% 2C3% 2C5% 2C6-tetrafluoroethoxyphenyl This substance, when used, has a number of things to pay attention to and needs to be treated with caution.
First, it concerns its toxicity. This substance may be toxic to a certain extent, and safety procedures must be strictly followed when operating. Make sure that the operator wears appropriate protective equipment, such as protective clothing, gloves, goggles, etc., to prevent it from coming into contact with the skin and eyes. And the operation is suitable for well-ventilated places. If it is in a closed space, its volatile gas may cause poisoning.
The second is its stability. 2% 2C3% 2C5% 2C6-tetrafluoroethoxybenzene may be unstable under specific conditions. When exposed to heat, light, or mixed with certain chemicals, or cause chemical reactions, cause their deterioration, or produce dangerous products. Therefore, when storing, it should be placed in a cool, dry and dark place, away from fire and heat sources, and should not be co-stored with incompatible chemicals.
Third, accurate use. Due to its special nature, the measurement must be accurate during use. A slight deviation may lead to the error of the experimental results, or in industrial production, affect the quality of the product. When operating, it is advisable to use precision measuring tools, according to the established process and ratio.
Fourth, waste disposal. After use, the generated waste must not be discarded at will. It needs to be properly disposed of in accordance with relevant environmental regulations. Because it may contain toxic ingredients, if not properly disposed of, it will pollute the environment and endanger the ecology. Or hand it over to a professional organization, or degrade and neutralize it according to a specific method to reduce its harm.
All of these are the keys to pay attention when using 2% 2C3% 2C5% 2C6-tetrafluoroethoxy phenyl, and must not be negligent to ensure safe and smooth operation.
First, it concerns its toxicity. This substance may be toxic to a certain extent, and safety procedures must be strictly followed when operating. Make sure that the operator wears appropriate protective equipment, such as protective clothing, gloves, goggles, etc., to prevent it from coming into contact with the skin and eyes. And the operation is suitable for well-ventilated places. If it is in a closed space, its volatile gas may cause poisoning.
The second is its stability. 2% 2C3% 2C5% 2C6-tetrafluoroethoxybenzene may be unstable under specific conditions. When exposed to heat, light, or mixed with certain chemicals, or cause chemical reactions, cause their deterioration, or produce dangerous products. Therefore, when storing, it should be placed in a cool, dry and dark place, away from fire and heat sources, and should not be co-stored with incompatible chemicals.
Third, accurate use. Due to its special nature, the measurement must be accurate during use. A slight deviation may lead to the error of the experimental results, or in industrial production, affect the quality of the product. When operating, it is advisable to use precision measuring tools, according to the established process and ratio.
Fourth, waste disposal. After use, the generated waste must not be discarded at will. It needs to be properly disposed of in accordance with relevant environmental regulations. Because it may contain toxic ingredients, if not properly disposed of, it will pollute the environment and endanger the ecology. Or hand it over to a professional organization, or degrade and neutralize it according to a specific method to reduce its harm.
All of these are the keys to pay attention when using 2% 2C3% 2C5% 2C6-tetrafluoroethoxy phenyl, and must not be negligent to ensure safe and smooth operation.
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