Linshang Chemical
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2,5 -Dichloro-4-(1,1,2,3,33,-Hexafluoropropoxy) Nitrobenzene
Linshang Chemical
|
HS Code |
628200 |
| Chemical Formula | C6H2Cl2F6NO4 |
| Molecular Weight | 329.98 |
As an accredited 2,5 -Dichloro-4-(1,1,2,3,33,-Hexafluoropropoxy) Nitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 2,5 - dichloro - 4 - (1,1,2,3,3,3 - hexafluoropropoxy) nitrobenzene in sealed container. |
| Storage | 2,5 - dichloro - 4 - (1,1,2,3,3,3 - hexafluoropropoxy) nitrobenzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and incompatible substances. Store in tightly sealed containers to prevent leakage and exposure to air or moisture, ensuring its stability and minimizing potential safety risks. |
| Shipping | 2,5 - dichloro - 4 - (1,1,2,3,3,3 - hexafluoropropoxy) nitrobenzene is shipped in well - sealed, corrosion - resistant containers. Compliance with hazardous chemical shipping regulations ensures safe transportation, avoiding exposure and environmental risks. |
Competitive 2,5 -Dichloro-4-(1,1,2,3,33,-Hexafluoropropoxy) Nitrobenzene 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
Where to Buy 2,5 -Dichloro-4-(1,1,2,3,33,-Hexafluoropropoxy) Nitrobenzene in China?
As a trusted 2,5 -Dichloro-4-(1,1,2,3,33,-Hexafluoropropoxy) Nitrobenzene manufacturer, we deliver:
Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements.
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As a leading 2,5 -Dichloro-4-(1,1,2,3,33,-Hexafluoropropoxy) Nitrobenzene 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 main use of 2,5-dichloro-4- (1,1,2,3,3,3-hexafluoropropoxy) nitrobenzene
2% 2C5-dioxy-4- (1,1,2,3,3,3-hexafluoropropoxy) pyrimidine has critical uses in many fields.
In the field of medicine, it is a key intermediate for the preparation of specific new antiviral drugs. After a series of chemical reactions, it can be cleverly combined with other active groups to shape drug molecules with high affinity and inhibitory activity for specific viruses. For example, in the study of some RNA viruses, drug molecules built on this basis can precisely act on the replication process of the virus, successfully blocking the proliferation of the virus in the host, and opening up a new path for the development of antiviral drugs.
In the field of pesticides, it exhibits excellent biological activity as a core component of high-efficiency insecticides and fungicides. With its unique chemical structure, it can interfere with the nervous system of pests or the metabolic pathways of pathogens, achieving efficient control effects. For example, when controlling pests and diseases in orchards and farmland, pesticide formulations containing this ingredient can effectively inhibit a variety of common pests and pathogens, and the impact on the environment is relatively slight, and the residue is low, which effectively guarantees the quality and safety of agricultural products.
In the field of materials science, 2% 2C5-dioxy-4 - (1,1,2,3,3,3-hexafluoropropoxy) pyrimidine can be used to prepare polymer materials with excellent performance. In the polymerization reaction, it participates as a functional monomer, endowing polymer materials with properties such as excellent thermal stability, chemical stability, and corrosion resistance. Such polymer materials are widely used in high-end fields such as aerospace, electronics, and electrical appliances, such as the manufacture of high-temperature components for aircraft engines, protective coatings for electronic chips, etc., which greatly enhance the performance and service life of related materials.
In the field of medicine, it is a key intermediate for the preparation of specific new antiviral drugs. After a series of chemical reactions, it can be cleverly combined with other active groups to shape drug molecules with high affinity and inhibitory activity for specific viruses. For example, in the study of some RNA viruses, drug molecules built on this basis can precisely act on the replication process of the virus, successfully blocking the proliferation of the virus in the host, and opening up a new path for the development of antiviral drugs.
In the field of pesticides, it exhibits excellent biological activity as a core component of high-efficiency insecticides and fungicides. With its unique chemical structure, it can interfere with the nervous system of pests or the metabolic pathways of pathogens, achieving efficient control effects. For example, when controlling pests and diseases in orchards and farmland, pesticide formulations containing this ingredient can effectively inhibit a variety of common pests and pathogens, and the impact on the environment is relatively slight, and the residue is low, which effectively guarantees the quality and safety of agricultural products.
In the field of materials science, 2% 2C5-dioxy-4 - (1,1,2,3,3,3-hexafluoropropoxy) pyrimidine can be used to prepare polymer materials with excellent performance. In the polymerization reaction, it participates as a functional monomer, endowing polymer materials with properties such as excellent thermal stability, chemical stability, and corrosion resistance. Such polymer materials are widely used in high-end fields such as aerospace, electronics, and electrical appliances, such as the manufacture of high-temperature components for aircraft engines, protective coatings for electronic chips, etc., which greatly enhance the performance and service life of related materials.
What are the physical properties of 2,5-dichloro-4- (1,1,2,3,3,3-hexafluoropropoxy) nitrobenzene
2% 2C5 -dioxo-4- (1,1,2,3,3,3 -hexafluoropropoxy) quinazoline, the physical properties of this substance are as follows:
Its properties may be crystalline solids, because the molecular structure contains specific fluorine atoms and complex quinazoline rings, which cause it to have a certain melting point. Fluorine atoms have high electronegativity, which will affect the intermolecular force and change the melting point compared to similar compounds without fluorine.
In terms of solubility, the dissolution in organic solvents is special in view of the fact that there are both hydrophobic fluoroalkyl groups and nitrogen-containing heterocycles in the molecule. In non-polar or weakly polar organic solvents, such as toluene and dichloromethane, there should be a certain solubility, because hydrophobic fluoroalkyl groups can interact with organic solvents; while in highly polar solvents, such as water, the solubility may be very small, because of the hydrophobicity of the overall structure.
The density of this substance is also affected by the molecular structure. The relative mass of fluorine atoms is large and the atomic radius is small, which makes the molecule pack more tightly, or causes its density to be higher than that of common organic compounds without fluorine.
Its stability is quite high due to the conjugation system of quinazoline rings and the stabilization of fluorine atoms. The conjugated structure of the quinazoline ring makes the electron cloud uniformly distributed and enhances the stability of the molecule; the C-F bond energy formed by the fluorine atom and the carbon atom is large, which further enhances the stability of the structure and makes it less prone to chemical reactions under normal conditions.
In addition, the volatility of this substance is low. Due to the existence of certain forces between molecules and the relatively complex structure, the energy required for the molecule to transform from the liquid state to the gas state is high, so the degree of volatilization is limited at room temperature and pressure.
Its properties may be crystalline solids, because the molecular structure contains specific fluorine atoms and complex quinazoline rings, which cause it to have a certain melting point. Fluorine atoms have high electronegativity, which will affect the intermolecular force and change the melting point compared to similar compounds without fluorine.
In terms of solubility, the dissolution in organic solvents is special in view of the fact that there are both hydrophobic fluoroalkyl groups and nitrogen-containing heterocycles in the molecule. In non-polar or weakly polar organic solvents, such as toluene and dichloromethane, there should be a certain solubility, because hydrophobic fluoroalkyl groups can interact with organic solvents; while in highly polar solvents, such as water, the solubility may be very small, because of the hydrophobicity of the overall structure.
The density of this substance is also affected by the molecular structure. The relative mass of fluorine atoms is large and the atomic radius is small, which makes the molecule pack more tightly, or causes its density to be higher than that of common organic compounds without fluorine.
Its stability is quite high due to the conjugation system of quinazoline rings and the stabilization of fluorine atoms. The conjugated structure of the quinazoline ring makes the electron cloud uniformly distributed and enhances the stability of the molecule; the C-F bond energy formed by the fluorine atom and the carbon atom is large, which further enhances the stability of the structure and makes it less prone to chemical reactions under normal conditions.
In addition, the volatility of this substance is low. Due to the existence of certain forces between molecules and the relatively complex structure, the energy required for the molecule to transform from the liquid state to the gas state is high, so the degree of volatilization is limited at room temperature and pressure.
Are the chemical properties of 2,5-dichloro-4- (1,1,2,3,3,3-hexafluoropropoxy) nitrobenzene stable?
2% 2C5-dioxy-4- (1,1,2,3,3,3-hexafluoropropoxy) quinazoline, the stability of this physical property depends on many factors.
In its structure, the groups of dioxy and hexafluoropropoxy have a great influence on its physical stability. Dioxy groups, due to their own electron cloud distribution and bond energy characteristics, can change the intermolecular forces. And hexafluoropropoxy, fluorine atoms have strong electronegativity, which can cause electron clouds to be biased, affect molecular polarity, and then play a role in their stability.
In terms of chemical environment, if it is in a high temperature environment, the bonds in the molecule may not be able to resist the impact of thermal energy, causing bond breakage and reducing stability. In case of specific chemical reagents, such as strong oxidizing agents or reducing agents, according to their reactivity or reaction with them, the original structure will be destroyed and its stability will be damaged.
In general conventional environments, if there is no strong external interference, the molecular structure may be relatively stable due to the mutual restraint of chemical bonds. In case of extreme conditions, its stability is difficult to guarantee. Therefore, the stability of 2% 2C5 -dioxy-4- (1,1,2,3,3,3 -hexafluoropropoxy) quinazoline cannot be generalized and must be judged in detail according to specific conditions.
In its structure, the groups of dioxy and hexafluoropropoxy have a great influence on its physical stability. Dioxy groups, due to their own electron cloud distribution and bond energy characteristics, can change the intermolecular forces. And hexafluoropropoxy, fluorine atoms have strong electronegativity, which can cause electron clouds to be biased, affect molecular polarity, and then play a role in their stability.
In terms of chemical environment, if it is in a high temperature environment, the bonds in the molecule may not be able to resist the impact of thermal energy, causing bond breakage and reducing stability. In case of specific chemical reagents, such as strong oxidizing agents or reducing agents, according to their reactivity or reaction with them, the original structure will be destroyed and its stability will be damaged.
In general conventional environments, if there is no strong external interference, the molecular structure may be relatively stable due to the mutual restraint of chemical bonds. In case of extreme conditions, its stability is difficult to guarantee. Therefore, the stability of 2% 2C5 -dioxy-4- (1,1,2,3,3,3 -hexafluoropropoxy) quinazoline cannot be generalized and must be judged in detail according to specific conditions.
What is the production process of 2,5-dichloro-4- (1,1,2,3,3,3-hexafluoropropoxy) nitrobenzene?
The production process of 2% 2C5-dioxy-4- (1,1,2,3,3,3-hexafluoropropoxy) pyridine is a delicate and complex process. This process requires many steps, each step needs to be precisely operated and strictly controlled.
In the initial stage, high-quality raw materials need to be carefully selected to ensure that each ingredient is pure and free of impurities, laying a solid foundation for subsequent reactions. After the raw materials are properly prepared, the key reaction link is started. During this process, the regulation of reaction conditions is crucial, such as temperature, pressure, reaction time and catalyst dosage, all need to be precisely pinched. If the temperature is too high or too low, it may cause the reaction to deviate from the expected path, generate impurities or cause the reaction to be incomplete; the control of pressure should not be underestimated, and the appropriate pressure can promote the reaction to proceed efficiently in the target direction.
Under a specific temperature and pressure environment, the raw materials can be fully reacted under the action of the catalyst. The choice of this catalyst is also very critical, and its activity and selectivity are directly related to the rate of the reaction and the purity of the product. After the reaction is completed, the product is often mixed with impurities such as unreacted raw materials, by-products and catalysts, so fine separation and purification operations are required.
The separation process usually relies on various technical means such as distillation, extraction, crystallization, etc., to effectively separate the target product and impurities according to the differences in the physical and chemical properties of each component. After purification, strict quality inspection of the product is required. Advanced analytical instruments, such as chromatographs, spectrometers, etc., are used to accurately determine the purity and structure of the product to ensure that it meets the established Quality Standards.
The entire production process is like a precise symphony, and all links are closely coordinated. Any omission at any place may affect the quality of the final product. Only by strictly following this well-designed process route can high-quality 2% 2C5-dioxy-4- (1,1,2,3,3,3-hexafluoropropoxy) pyridine be produced stably and efficiently.
In the initial stage, high-quality raw materials need to be carefully selected to ensure that each ingredient is pure and free of impurities, laying a solid foundation for subsequent reactions. After the raw materials are properly prepared, the key reaction link is started. During this process, the regulation of reaction conditions is crucial, such as temperature, pressure, reaction time and catalyst dosage, all need to be precisely pinched. If the temperature is too high or too low, it may cause the reaction to deviate from the expected path, generate impurities or cause the reaction to be incomplete; the control of pressure should not be underestimated, and the appropriate pressure can promote the reaction to proceed efficiently in the target direction.
Under a specific temperature and pressure environment, the raw materials can be fully reacted under the action of the catalyst. The choice of this catalyst is also very critical, and its activity and selectivity are directly related to the rate of the reaction and the purity of the product. After the reaction is completed, the product is often mixed with impurities such as unreacted raw materials, by-products and catalysts, so fine separation and purification operations are required.
The separation process usually relies on various technical means such as distillation, extraction, crystallization, etc., to effectively separate the target product and impurities according to the differences in the physical and chemical properties of each component. After purification, strict quality inspection of the product is required. Advanced analytical instruments, such as chromatographs, spectrometers, etc., are used to accurately determine the purity and structure of the product to ensure that it meets the established Quality Standards.
The entire production process is like a precise symphony, and all links are closely coordinated. Any omission at any place may affect the quality of the final product. Only by strictly following this well-designed process route can high-quality 2% 2C5-dioxy-4- (1,1,2,3,3,3-hexafluoropropoxy) pyridine be produced stably and efficiently.
Precautions for storing and transporting 2,5-dichloro-4- (1,1,2,3,3,3-hexafluoropropoxy) nitrobenzene
2% 2C5-dioxy-4- (1,1,2,3,3,3-hexafluoropropoxy) quinoline requires attention to many matters during storage and transportation.
First, because of its chemical activity, it must be stored in a dry, cool and well-ventilated place. Humid environments can easily cause it to react with water vapor, change chemical properties, and then affect quality and performance. A cool place can prevent decomposition and volatilization caused by excessive temperature, ensuring its chemical stability. Good ventilation can disperse harmful gases that may evaporate in time to avoid potential safety hazards caused by accumulation.
Second, storage containers need to be adapted. Containers with good corrosion resistance and sealing should be selected. The substance may react chemically with certain materials, such as ordinary metal containers, which may be corroded, not only damaging the container, but also contaminating the substance. Sealing well can prevent reactions such as oxidation in contact with air, and maintain its purity and quality.
Third, be well protected during transportation. Take stable measures to avoid collisions and vibrations to prevent material leakage caused by container damage. According to its characteristics, operate according to the regulations for the transportation of hazardous chemicals, and be equipped with corresponding emergency treatment equipment and protective equipment. Once leaked, it can be responded to in time to reduce hazards.
Fourth, it should be stored and transported separately from other chemicals. Due to its chemical properties, it may react with other substances, causing serious consequences such as combustion and explosion. For example, strong oxidants, strong acids and alkalis, etc., must be isolated to ensure the safety of storage and transportation.
In short, the storage and transportation of 2% 2C5-dioxy-4- (1,1,2,3,3,3-hexafluoropropoxy) quinoline, from the environment, containers, protection to isolation, etc., must be strictly controlled to ensure the safety of personnel, the environment is not polluted and the quality of materials is not damaged.
First, because of its chemical activity, it must be stored in a dry, cool and well-ventilated place. Humid environments can easily cause it to react with water vapor, change chemical properties, and then affect quality and performance. A cool place can prevent decomposition and volatilization caused by excessive temperature, ensuring its chemical stability. Good ventilation can disperse harmful gases that may evaporate in time to avoid potential safety hazards caused by accumulation.
Second, storage containers need to be adapted. Containers with good corrosion resistance and sealing should be selected. The substance may react chemically with certain materials, such as ordinary metal containers, which may be corroded, not only damaging the container, but also contaminating the substance. Sealing well can prevent reactions such as oxidation in contact with air, and maintain its purity and quality.
Third, be well protected during transportation. Take stable measures to avoid collisions and vibrations to prevent material leakage caused by container damage. According to its characteristics, operate according to the regulations for the transportation of hazardous chemicals, and be equipped with corresponding emergency treatment equipment and protective equipment. Once leaked, it can be responded to in time to reduce hazards.
Fourth, it should be stored and transported separately from other chemicals. Due to its chemical properties, it may react with other substances, causing serious consequences such as combustion and explosion. For example, strong oxidants, strong acids and alkalis, etc., must be isolated to ensure the safety of storage and transportation.
In short, the storage and transportation of 2% 2C5-dioxy-4- (1,1,2,3,3,3-hexafluoropropoxy) quinoline, from the environment, containers, protection to isolation, etc., must be strictly controlled to ensure the safety of personnel, the environment is not polluted and the quality of materials is not damaged.
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