Linshang Chemical
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1,2,3,4,5-Pentafluoro-6-(Trichloromethyl)Benzene
Linshang Chemical
|
HS Code |
675817 |
| Chemical Formula | C7Cl3F5 |
| Molar Mass | 297.42 g/mol |
| Appearance | likely a colorless to pale - colored liquid |
| Solubility In Water | very low, as it is a non - polar aromatic compound |
| Solubility In Organic Solvents | soluble in common non - polar organic solvents like hexane, toluene |
| Vapor Pressure | low vapor pressure at room temperature due to relatively high molar mass |
| Stability | stable under normal conditions, but may react with strong oxidizing or reducing agents |
As an accredited 1,2,3,4,5-Pentafluoro-6-(Trichloromethyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500 - gram bottle of 1,2,3,4,5 - pentafluoro - 6-(trichloromethyl)benzene, well - sealed. |
| Storage | 1,2,3,4,5 - Pentafluoro - 6 - (trichloromethyl)benzene should be stored in a cool, well - ventilated area, away from heat sources and ignition points. Keep it in a tightly closed container made of corrosion - resistant materials, as it may react with certain substances. Store separately from oxidizing agents, reducing agents, and incompatible chemicals to prevent hazardous reactions. |
| Shipping | 1,2,3,4,5 - Pentafluoro - 6 - (trichloromethyl)benzene is shipped in specialized, tightly - sealed containers. It follows strict hazardous chemical shipping regulations to prevent leakage and ensure safe transportation due to its potentially harmful nature. |
Competitive 1,2,3,4,5-Pentafluoro-6-(Trichloromethyl)Benzene 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 1,2,3,4,5-Pentafluoro-6-(Trichloromethyl)Benzene 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 this compound 1,2,3,4,5-pentafluoro-6- (trichloromethyl) benzene?
This compound, 1,2,3,4,5-pentanediol-6- (trifluoromethyl) naphthalene, has important uses in many fields.
In the field of medicinal chemistry, it can be used as a key intermediate in drug synthesis. Due to its unique chemical structure, trifluoromethyl can significantly change the physical, chemical and biological activities of compounds. For example, trifluoromethyl has strong electron absorption and can adjust the electron cloud distribution of molecules, thereby enhancing the ability of drugs to bind to targets and improving the efficacy of drugs. With the help of this compound, a series of drug molecules with specific pharmacological activities can be synthesized for the treatment of various diseases such as cardiovascular diseases, neurological diseases and cancer.
In the field of materials science, it can be used to prepare high-performance functional materials. The pentanediol structure gives the material certain flexibility and hydrophilicity, while trifluoromethyl can enhance the chemical stability, corrosion resistance and low surface energy of the material. For example, when preparing special coating materials, the addition of this compound can make the coating have excellent waterproof, oil-proof and anti-fouling properties, which are widely used in construction, automotive and aerospace fields. At the same time, in electronic materials, it can also optimize the electrical properties and thermal stability of the material, and improve the performance and reliability of electronic devices.
In the field of organic synthetic chemistry, it is an extremely useful synthetic block. With its multiple reactivity checking points, it can construct more complex organic molecular structures through various organic reactions, such as esterification, etherification, oxidation, etc. Organic chemists can use it to design and synthesize organic compounds with novel structures and functions, providing new material basis and research ideas for the development of organic synthetic chemistry.
In the field of medicinal chemistry, it can be used as a key intermediate in drug synthesis. Due to its unique chemical structure, trifluoromethyl can significantly change the physical, chemical and biological activities of compounds. For example, trifluoromethyl has strong electron absorption and can adjust the electron cloud distribution of molecules, thereby enhancing the ability of drugs to bind to targets and improving the efficacy of drugs. With the help of this compound, a series of drug molecules with specific pharmacological activities can be synthesized for the treatment of various diseases such as cardiovascular diseases, neurological diseases and cancer.
In the field of materials science, it can be used to prepare high-performance functional materials. The pentanediol structure gives the material certain flexibility and hydrophilicity, while trifluoromethyl can enhance the chemical stability, corrosion resistance and low surface energy of the material. For example, when preparing special coating materials, the addition of this compound can make the coating have excellent waterproof, oil-proof and anti-fouling properties, which are widely used in construction, automotive and aerospace fields. At the same time, in electronic materials, it can also optimize the electrical properties and thermal stability of the material, and improve the performance and reliability of electronic devices.
In the field of organic synthetic chemistry, it is an extremely useful synthetic block. With its multiple reactivity checking points, it can construct more complex organic molecular structures through various organic reactions, such as esterification, etherification, oxidation, etc. Organic chemists can use it to design and synthesize organic compounds with novel structures and functions, providing new material basis and research ideas for the development of organic synthetic chemistry.
What are the physical properties of 1,2,3,4,5-pentafluoro-6- (trichloromethyl) benzene?
The physical properties of 1% 2C2% 2C3% 2C4% 2C5-pentamethyl-6- (trimethylphenyl) naphthalene are as follows:
The appearance of this compound may be in a crystalline state, and it is usually a white to light yellow solid. Its melting point is quite critical. It has been calculated by many researchers and is about a specific temperature range. This temperature range has a great impact on its application in various scenarios. The melting point determines the heat required for it to change from a solid state to a liquid state, which is related to whether it can exist stably under specific conditions, or at what temperature the phase change occurs.
The boiling point is also one of the important physical properties. In a certain pressure environment, at a certain temperature, the substance will change from a liquid state to a gas state, and this temperature is the boiling point. Knowing the boiling point is crucial in the process of separating and purifying this compound, and is the basis for precise control of the process conditions. The density of
cannot be ignored, reflecting the mass of the substance per unit volume. Through accurate measurement, its density value can be known. This value provides an important reference for judging its sinking and floating in different media and the proportion of volume when mixed with other substances. In terms of solubility, the substance exhibits certain solubility properties in organic solvents. It can be dissolved in some common organic solvents, such as ethanol, ether, etc., but it is less soluble in water. This property determines its dispersion and reaction behavior in different solvent systems, and has far-reaching impact on related chemical synthesis, preparation and other application fields.
In addition, its crystal structure has also been deeply investigated. By means of advanced techniques such as X-ray diffraction, the arrangement of its molecules in the lattice is revealed. This structure is closely related to the above physical properties, explaining the essence of the macroscopic properties of matter at the microscopic level.
The appearance of this compound may be in a crystalline state, and it is usually a white to light yellow solid. Its melting point is quite critical. It has been calculated by many researchers and is about a specific temperature range. This temperature range has a great impact on its application in various scenarios. The melting point determines the heat required for it to change from a solid state to a liquid state, which is related to whether it can exist stably under specific conditions, or at what temperature the phase change occurs.
The boiling point is also one of the important physical properties. In a certain pressure environment, at a certain temperature, the substance will change from a liquid state to a gas state, and this temperature is the boiling point. Knowing the boiling point is crucial in the process of separating and purifying this compound, and is the basis for precise control of the process conditions. The density of
cannot be ignored, reflecting the mass of the substance per unit volume. Through accurate measurement, its density value can be known. This value provides an important reference for judging its sinking and floating in different media and the proportion of volume when mixed with other substances. In terms of solubility, the substance exhibits certain solubility properties in organic solvents. It can be dissolved in some common organic solvents, such as ethanol, ether, etc., but it is less soluble in water. This property determines its dispersion and reaction behavior in different solvent systems, and has far-reaching impact on related chemical synthesis, preparation and other application fields.
In addition, its crystal structure has also been deeply investigated. By means of advanced techniques such as X-ray diffraction, the arrangement of its molecules in the lattice is revealed. This structure is closely related to the above physical properties, explaining the essence of the macroscopic properties of matter at the microscopic level.
Is 1,2,3,4,5-pentafluoro-6- (trichloromethyl) benzene chemically stable?
The chemical stability of "Wuhe" referred to by 1% 2C2% 2C3% 2C4% 2C5 and 6- (tritium methyl) benzene needs to be studied in detail.
The stability of a chemical substance depends on its molecular structure, chemical bond energy and many other factors. For Wuhe, if viewed as a collection of water, water is a common and relatively stable compound. Its hydrogen and oxygen atoms are connected by covalent bonds, and the bond energy is quite high. To make it chemically change, specific conditions such as high temperature and chemical reactants are often required.
As for 6- (tritium methyl) benzene, the benzene ring itself has a conjugated system, which gives benzene a certain stability. However, the introduction of tritium methyl may have other effects. Tritium is a radioactive isotope of hydrogen, and its nucleus contains two neutrons and one proton, which is more two neutrons than that of ordinary hydrogen atoms. This extra neutron may cause slight changes in the interaction between atoms, and the radioactivity of tritium may affect the molecular stability. Tritium methyl is connected to the benzene ring, or changes the electron cloud distribution of the benzene ring, which affects its chemical activity.
But only for this statement, its exact structure and surrounding chemical environment are not known, and it is difficult to determine its stability. It may be necessary to know more about its spatial configuration, the interaction of surrounding functional groups, and the external conditions such as temperature and pressure in order to obtain a definite conclusion of its chemical stability.
The stability of a chemical substance depends on its molecular structure, chemical bond energy and many other factors. For Wuhe, if viewed as a collection of water, water is a common and relatively stable compound. Its hydrogen and oxygen atoms are connected by covalent bonds, and the bond energy is quite high. To make it chemically change, specific conditions such as high temperature and chemical reactants are often required.
As for 6- (tritium methyl) benzene, the benzene ring itself has a conjugated system, which gives benzene a certain stability. However, the introduction of tritium methyl may have other effects. Tritium is a radioactive isotope of hydrogen, and its nucleus contains two neutrons and one proton, which is more two neutrons than that of ordinary hydrogen atoms. This extra neutron may cause slight changes in the interaction between atoms, and the radioactivity of tritium may affect the molecular stability. Tritium methyl is connected to the benzene ring, or changes the electron cloud distribution of the benzene ring, which affects its chemical activity.
But only for this statement, its exact structure and surrounding chemical environment are not known, and it is difficult to determine its stability. It may be necessary to know more about its spatial configuration, the interaction of surrounding functional groups, and the external conditions such as temperature and pressure in order to obtain a definite conclusion of its chemical stability.
What are the methods for preparing 1,2,3,4,5-pentafluoro-6- (trichloromethyl) benzene?
To prepare 1,2,3,4,5-pentene-6- (trimethyl) benzene, the following approaches can be started.
First, suitable aromatic derivatives can be started. Find benzene ring compounds with appropriate substituents, and introduce halogen atoms at specific positions in the benzene ring by halogenation reaction. If benzene is used as the starting material, halogenated benzene can be prepared by the action of halogenating agents. After that, with the help of metal-organic reagents, such as Grignard reagents, react with halogenated benzene to form carbon-carbon bonds, and introduce structural fragments containing alkenyl groups and methyl groups. For example, by reacting halogenated benzene with Grignard reagents such as allyl magnesium halide in a suitable solvent, such as anhydrous ether or tetrahydrofuran, after subsequent treatment, it is expected to obtain benzene derivatives containing alkenyl substitutions. Then through appropriate methylation reagents, such as the combination of iodomethane and base, under specific conditions, methyl groups are introduced into the molecule to gradually construct the structure of the target molecule.
Second, a stepwise synthesis strategy is adopted. First, the carbon chain structure containing alkenyl groups is constructed. Acetylene or other alkynes are used as raw materials and selectively hydrogenated to obtain the corresponding alkenes. If acetylene is catalyzed by Lindela catalyst, ethylene can be obtained. Using ethylene and halogenated alkanes under the action of a suitable catalyst, the carbon chain is increased through an addition reaction. After that, the constructed alkenyl-containing carbon chain is connected to the benzene ring. The Fourier-Gram reaction can be used to react the alkenyl-containing halogenated hydrocarbon with benzene under the action of a Lewis acid catalyst such as aluminum trichloride, and the alkenyl group is introduced into the benzene ring. Finally, the resulting product is methylated to achieve the preparation of 1,2,3,4,5-pentene-6- (trimethyl) benzene.
Third, the cyclization reaction strategy can be considered. A chain-like compound containing multiple alkenyl groups and appropriate substituents is selected, and under suitable catalysts and reaction conditions, the cyclization reaction occurs in the molecule to form a benzene ring structure. For example, a chain-like diolefin derivative containing five conjugated alkenyl groups and appropriate methyl substitutions is used as a raw material. Under the catalysis of specific catalysts such as metal complexes, an intramolecular cyclization reaction occurs to construct a benzene ring skeleton, and then the target product is obtained. In this process, the reaction conditions need to be carefully adjusted to ensure the regioselectivity and stereoselectivity of the cyclization reaction to obtain the desired 1,2,3,4,5-pentene-6- (trimethyl) benzene.
First, suitable aromatic derivatives can be started. Find benzene ring compounds with appropriate substituents, and introduce halogen atoms at specific positions in the benzene ring by halogenation reaction. If benzene is used as the starting material, halogenated benzene can be prepared by the action of halogenating agents. After that, with the help of metal-organic reagents, such as Grignard reagents, react with halogenated benzene to form carbon-carbon bonds, and introduce structural fragments containing alkenyl groups and methyl groups. For example, by reacting halogenated benzene with Grignard reagents such as allyl magnesium halide in a suitable solvent, such as anhydrous ether or tetrahydrofuran, after subsequent treatment, it is expected to obtain benzene derivatives containing alkenyl substitutions. Then through appropriate methylation reagents, such as the combination of iodomethane and base, under specific conditions, methyl groups are introduced into the molecule to gradually construct the structure of the target molecule.
Second, a stepwise synthesis strategy is adopted. First, the carbon chain structure containing alkenyl groups is constructed. Acetylene or other alkynes are used as raw materials and selectively hydrogenated to obtain the corresponding alkenes. If acetylene is catalyzed by Lindela catalyst, ethylene can be obtained. Using ethylene and halogenated alkanes under the action of a suitable catalyst, the carbon chain is increased through an addition reaction. After that, the constructed alkenyl-containing carbon chain is connected to the benzene ring. The Fourier-Gram reaction can be used to react the alkenyl-containing halogenated hydrocarbon with benzene under the action of a Lewis acid catalyst such as aluminum trichloride, and the alkenyl group is introduced into the benzene ring. Finally, the resulting product is methylated to achieve the preparation of 1,2,3,4,5-pentene-6- (trimethyl) benzene.
Third, the cyclization reaction strategy can be considered. A chain-like compound containing multiple alkenyl groups and appropriate substituents is selected, and under suitable catalysts and reaction conditions, the cyclization reaction occurs in the molecule to form a benzene ring structure. For example, a chain-like diolefin derivative containing five conjugated alkenyl groups and appropriate methyl substitutions is used as a raw material. Under the catalysis of specific catalysts such as metal complexes, an intramolecular cyclization reaction occurs to construct a benzene ring skeleton, and then the target product is obtained. In this process, the reaction conditions need to be carefully adjusted to ensure the regioselectivity and stereoselectivity of the cyclization reaction to obtain the desired 1,2,3,4,5-pentene-6- (trimethyl) benzene.
What are the environmental effects of 1,2,3,4,5-pentafluoro-6- (trichloromethyl) benzene?
1% 2C2% 2C3% 2C4% 2C5-Wuhe-6- (trichloromethyl) benzene is involved in the environment, which is quite complex and crucial. Let me explain in detail.
First word water environment. If this compound enters the water body, it may accumulate in the water body due to its chemical characteristics, or it is difficult for aquatic organisms to decompose, resulting in its accumulation in the water body. Aquatic organisms such as fish, shrimp, shellfish, etc. live in this polluted water for a long time, and their physiological functions are easily damaged. It may affect the reproduction of organisms, cause aberration in the development of larvae, decrease the population number, and cause imbalance in the aquatic ecosystem. And this substance is transmitted through the food chain layer by layer, or poses a potential threat to human health.
and soil. If 1% 2C2% 2C3% 2C4% 2C5-Wuhe-6- (trichloromethyl) benzene seeps into the soil, it will change the physical and chemical properties of the soil. Or affect the community structure and function of soil microorganisms, reducing microbial diversity. Microorganisms play a key role in soil nutrient cycling, organic matter decomposition and other processes. If they are affected, they will cause soil fertility to decline and hinder plant growth. Poor plant growth will affect the organisms that feed on plants, and then affect the energy flow and material circulation of terrestrial ecosystems.
Let's talk about the atmosphere. This compound evaporates to the atmosphere under specific conditions and will participate in photochemical reactions. It interacts with other pollutants in the atmosphere, or generates secondary pollutants, such as ozone, fine particulate matter, etc., which exacerbates the degree of air pollution, affects air quality, causes damage to the human respiratory system, cardiovascular system, etc., and also affects the climate, making climate change more complex.
In short, 1% 2C2% 2C3% 2C4% 2C5 - Wuhe - 6 - (trichloromethyl) benzene has a negative impact on environmental factors such as water, soil, and air. It should be treated with caution and strictly controlled to protect the safety of the ecological environment.
First word water environment. If this compound enters the water body, it may accumulate in the water body due to its chemical characteristics, or it is difficult for aquatic organisms to decompose, resulting in its accumulation in the water body. Aquatic organisms such as fish, shrimp, shellfish, etc. live in this polluted water for a long time, and their physiological functions are easily damaged. It may affect the reproduction of organisms, cause aberration in the development of larvae, decrease the population number, and cause imbalance in the aquatic ecosystem. And this substance is transmitted through the food chain layer by layer, or poses a potential threat to human health.
and soil. If 1% 2C2% 2C3% 2C4% 2C5-Wuhe-6- (trichloromethyl) benzene seeps into the soil, it will change the physical and chemical properties of the soil. Or affect the community structure and function of soil microorganisms, reducing microbial diversity. Microorganisms play a key role in soil nutrient cycling, organic matter decomposition and other processes. If they are affected, they will cause soil fertility to decline and hinder plant growth. Poor plant growth will affect the organisms that feed on plants, and then affect the energy flow and material circulation of terrestrial ecosystems.
Let's talk about the atmosphere. This compound evaporates to the atmosphere under specific conditions and will participate in photochemical reactions. It interacts with other pollutants in the atmosphere, or generates secondary pollutants, such as ozone, fine particulate matter, etc., which exacerbates the degree of air pollution, affects air quality, causes damage to the human respiratory system, cardiovascular system, etc., and also affects the climate, making climate change more complex.
In short, 1% 2C2% 2C3% 2C4% 2C5 - Wuhe - 6 - (trichloromethyl) benzene has a negative impact on environmental factors such as water, soil, and air. It should be treated with caution and strictly controlled to protect the safety of the ecological environment.
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