Linshang Chemical
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Benzene, 1-Chloro-5-Fluoro-2-Methyl-4-Nitro-
Linshang Chemical
|
HS Code |
994118 |
| Chemical Formula | C7H5ClFNO2 |
| Molar Mass | 191.57 g/mol |
As an accredited Benzene, 1-Chloro-5-Fluoro-2-Methyl-4-Nitro- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 1 - chloro - 5 - fluoro - 2 - methyl - 4 - nitro - benzene in a sealed chemical - grade bottle. |
| Storage | 1 - Chloro - 5 - fluoro - 2 - methyl - 4 - nitro - benzene should be stored in a cool, dry, well - ventilated area away from heat sources and ignition sources. It should be kept in a tightly - sealed container, preferably made of corrosion - resistant materials. Separate it from oxidizing agents, reducing agents, and other incompatible substances to prevent potential chemical reactions. |
| Shipping | For the chemical “Benzene, 1 - chloro - 5 - fluoro - 2 - methyl - 4 - nitro -”, it should be shipped in accordance with hazardous chemical regulations. Use proper, labeled containers, and ensure transportation by carriers licensed for such substances. |
Competitive Benzene, 1-Chloro-5-Fluoro-2-Methyl-4-Nitro- 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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What are the physical properties of 1-chloro-5-fluoro-2-methyl-4-nitrobenzene
1 + -Deuterium-5 + -tritium-2 + -methyl-4 + -hydroxy naphthalene, this substance is a special organic compound. Its physical properties are unique, let me tell them one by one.
First of all, the appearance, at room temperature, or a colorless to light yellow oily liquid, with a certain fluidity, can be seen under light flickering, just like a faint light looming in the middle.
In terms of boiling point, due to its intermolecular force and structure, the boiling point is quite high, about [X] ° C. This property makes it not easy to volatilize in ordinary temperature environments, and can exist relatively stably in specific systems. The melting point of
is at [Y] ° C, and it will change from liquid to solid at low temperature. During the morphological change, the molecular arrangement will tend to be orderly from disorder, just like the quiet change of the microscopic world.
In terms of solubility, the substance is difficult to dissolve in water, because water is a polar solvent, and the polarity of this compound is weak. According to the principle of similar miscibility, the two are difficult to fuse. However, it is soluble in many organic solvents, such as ethanol, ether, etc. In such solvents, it can be evenly dispersed, just like fish swimming in water, and they are compatible with each other.
The density is slightly larger than that of water. When mixed with water, it will slowly sink to the bottom of the water, like a pearl falling into the abyss, showing a layered state.
The refractive index also has a specific value. When light passes through this substance, the light path will be deflected accordingly according to its refractive index, just like light meandering in a microscopic maze following specific rules. This property may be potentially useful in the field of optics.
The above is a summary of the physical properties of this 1 + -deuterium-5 + -tritium-2 + -methyl-4 + -hydroxynaphthalene.
First of all, the appearance, at room temperature, or a colorless to light yellow oily liquid, with a certain fluidity, can be seen under light flickering, just like a faint light looming in the middle.
In terms of boiling point, due to its intermolecular force and structure, the boiling point is quite high, about [X] ° C. This property makes it not easy to volatilize in ordinary temperature environments, and can exist relatively stably in specific systems. The melting point of
is at [Y] ° C, and it will change from liquid to solid at low temperature. During the morphological change, the molecular arrangement will tend to be orderly from disorder, just like the quiet change of the microscopic world.
In terms of solubility, the substance is difficult to dissolve in water, because water is a polar solvent, and the polarity of this compound is weak. According to the principle of similar miscibility, the two are difficult to fuse. However, it is soluble in many organic solvents, such as ethanol, ether, etc. In such solvents, it can be evenly dispersed, just like fish swimming in water, and they are compatible with each other.
The density is slightly larger than that of water. When mixed with water, it will slowly sink to the bottom of the water, like a pearl falling into the abyss, showing a layered state.
The refractive index also has a specific value. When light passes through this substance, the light path will be deflected accordingly according to its refractive index, just like light meandering in a microscopic maze following specific rules. This property may be potentially useful in the field of optics.
The above is a summary of the physical properties of this 1 + -deuterium-5 + -tritium-2 + -methyl-4 + -hydroxynaphthalene.
What are the chemical properties of 1-chloro-5-fluoro-2-methyl-4-nitrobenzene
"1 + -
Looking at its structure, there are functional groups such as methyl and carbonyl groups. The methyl group has a certain electron supply property, which can affect the electron cloud distribution of the molecule. Due to the action of the electron supply of the methyl group, the electron cloud density of the benzene ring connected to it can increase. In this way, during the electrophilic substitution reaction, the benzene ring is more vulnerable to the attack of electrophilic reagents, and the reactivity is improved.
And carbonyl is an electron-withdrawing group. Its powerful electron-absorbing effect can reduce the electron cloud density of the benzene ring. In the nucleophilic reaction, the carbon atom of the carbonyl group is positively charged and vulnerable to the attack of nucleophilic reagents, so nucleophilic addition and other reactions can occur.
Furthermore, the "Jiang" part of the compound (or a specific structural fragment, but the description is not detailed, it is only speculated), if it has structural characteristics such as unsaturated bonds, it will also participate in various addition, redox and other reactions.
In terms of solubility, because it contains polar carbonyl groups, it may have a certain solubility in polar solvents; however, there are non-polar parts such as benzene rings and methyl groups, which may also have a certain solubility in non-polar solvents.
As for stability, when the carbonyl group forms a conjugated system with the benzene ring, the molecular stability can be enhanced; however, if it is affected by external conditions such as high temperature, strong acid and base, its structure may change, triggering reactions such as hydrolysis and rearrangement.
In summary, the chemical properties of this compound are rich and diverse, and are influenced by the interaction of various functional groups and external conditions.
Looking at its structure, there are functional groups such as methyl and carbonyl groups. The methyl group has a certain electron supply property, which can affect the electron cloud distribution of the molecule. Due to the action of the electron supply of the methyl group, the electron cloud density of the benzene ring connected to it can increase. In this way, during the electrophilic substitution reaction, the benzene ring is more vulnerable to the attack of electrophilic reagents, and the reactivity is improved.
And carbonyl is an electron-withdrawing group. Its powerful electron-absorbing effect can reduce the electron cloud density of the benzene ring. In the nucleophilic reaction, the carbon atom of the carbonyl group is positively charged and vulnerable to the attack of nucleophilic reagents, so nucleophilic addition and other reactions can occur.
Furthermore, the "Jiang" part of the compound (or a specific structural fragment, but the description is not detailed, it is only speculated), if it has structural characteristics such as unsaturated bonds, it will also participate in various addition, redox and other reactions.
In terms of solubility, because it contains polar carbonyl groups, it may have a certain solubility in polar solvents; however, there are non-polar parts such as benzene rings and methyl groups, which may also have a certain solubility in non-polar solvents.
As for stability, when the carbonyl group forms a conjugated system with the benzene ring, the molecular stability can be enhanced; however, if it is affected by external conditions such as high temperature, strong acid and base, its structure may change, triggering reactions such as hydrolysis and rearrangement.
In summary, the chemical properties of this compound are rich and diverse, and are influenced by the interaction of various functional groups and external conditions.
What are the main uses of 1-chloro-5-fluoro-2-methyl-4-nitrobenzene?
The main use of 1 + -
in the synthesis of fragrances, 1 + -
- < 5 + - -2 + -methyl-4 + -propylbenzene can be used as a key raw material. Due to its unique chemical structure and odor characteristics, through a series of chemical reactions, it can be derived into fragrant and rich fragrances, which are used in cosmetics, perfumes, air fresheners and other products to enhance the uniqueness and elegance of its aroma.
In the field of medicinal chemistry, this compound also plays an important role. As an intermediate, it can be chemically modified and transformed to construct a molecular structure with specific pharmacological activities. With the ingenious means of organic synthesis, drugs for treating specific diseases can be synthesized, or the foundation for the development of new pharmaceutical varieties can be laid.
Furthermore, in the field of materials science, 1 + - 5 + - Jiang - 2 + - methyl - 4 + - propylbenzene or participate in the synthesis of polymer materials. By polymerizing with other monomers, polymer materials are endowed with specific properties, such as improving the solubility and thermal stability of materials, and expanding the application of materials in different fields.
To sum up, 1 + - 5 + - Jiang - 2 + - methyl - 4 + - propylbenzene, with its diverse chemical properties, plays a key role in many fields such as fragrances, medicine, and materials, providing an important material basis for the development of the chemical industry.
in the synthesis of fragrances, 1 + -
- < 5 + - -2 + -methyl-4 + -propylbenzene can be used as a key raw material. Due to its unique chemical structure and odor characteristics, through a series of chemical reactions, it can be derived into fragrant and rich fragrances, which are used in cosmetics, perfumes, air fresheners and other products to enhance the uniqueness and elegance of its aroma.
In the field of medicinal chemistry, this compound also plays an important role. As an intermediate, it can be chemically modified and transformed to construct a molecular structure with specific pharmacological activities. With the ingenious means of organic synthesis, drugs for treating specific diseases can be synthesized, or the foundation for the development of new pharmaceutical varieties can be laid.
Furthermore, in the field of materials science, 1 + - 5 + - Jiang - 2 + - methyl - 4 + - propylbenzene or participate in the synthesis of polymer materials. By polymerizing with other monomers, polymer materials are endowed with specific properties, such as improving the solubility and thermal stability of materials, and expanding the application of materials in different fields.
To sum up, 1 + - 5 + - Jiang - 2 + - methyl - 4 + - propylbenzene, with its diverse chemical properties, plays a key role in many fields such as fragrances, medicine, and materials, providing an important material basis for the development of the chemical industry.
What are the preparation methods of 1-chloro-5-fluoro-2-methyl-4-nitrobenzene
To prepare 1-bromo-5-pentene-2-methyl-4-carbonylbenzene, the method is as follows:
First take an appropriate amount of starting materials, pay attention to the purity and quality of the raw materials, which is related to the effect of the reaction. Benzene compounds with suitable substituents can be selected, supplemented by halogenated olefins containing alkenyl and bromine atoms, and reagents capable of introducing methyl and carbonyl groups.
In the reaction vessel, dissolve the raw materials in a suitable organic solvent, such as anhydrous ethyl ether, tetrahydrofuran, etc., to create a suitable reaction environment. Adding an appropriate amount of catalyst, the choice of this catalyst is very critical, depending on the reaction mechanism and substrate characteristics, such as some metal salt catalysts or organic base catalysts, which can accelerate the reaction process and promote the fracture and formation of chemical bonds.
Control the reaction temperature and time. The reaction may need to be initiated at low temperature or room temperature, and then moderately warmed according to the reaction process. During the reaction, close monitoring is required. The consumption of raw materials and the formation of products can be observed by means of thin-layer chromatography.
When the reaction reaches the desired degree, the reaction is terminated. Separate the product by a suitable method, such as by extraction, using the difference in solubility of the product and impurities in different solvents, and extract the product to a specific solvent layer. After that, the product is purified by drying, filtration, distillation, column chromatography and other fine separation methods to obtain high-purity 1-bromo-5-pentene-2-methyl-4-carbonyl benzene. The whole process must pay attention to the standard and safety of operation to ensure the smooth progress of the reaction, and the quality and yield of the product are excellent.
First take an appropriate amount of starting materials, pay attention to the purity and quality of the raw materials, which is related to the effect of the reaction. Benzene compounds with suitable substituents can be selected, supplemented by halogenated olefins containing alkenyl and bromine atoms, and reagents capable of introducing methyl and carbonyl groups.
In the reaction vessel, dissolve the raw materials in a suitable organic solvent, such as anhydrous ethyl ether, tetrahydrofuran, etc., to create a suitable reaction environment. Adding an appropriate amount of catalyst, the choice of this catalyst is very critical, depending on the reaction mechanism and substrate characteristics, such as some metal salt catalysts or organic base catalysts, which can accelerate the reaction process and promote the fracture and formation of chemical bonds.
Control the reaction temperature and time. The reaction may need to be initiated at low temperature or room temperature, and then moderately warmed according to the reaction process. During the reaction, close monitoring is required. The consumption of raw materials and the formation of products can be observed by means of thin-layer chromatography.
When the reaction reaches the desired degree, the reaction is terminated. Separate the product by a suitable method, such as by extraction, using the difference in solubility of the product and impurities in different solvents, and extract the product to a specific solvent layer. After that, the product is purified by drying, filtration, distillation, column chromatography and other fine separation methods to obtain high-purity 1-bromo-5-pentene-2-methyl-4-carbonyl benzene. The whole process must pay attention to the standard and safety of operation to ensure the smooth progress of the reaction, and the quality and yield of the product are excellent.
What are the environmental effects of 1-chloro-5-fluoro-2-methyl-4-nitrobenzene?
The environmental implications of 1 + -alkane-5 + -ene-2 + -methyl-4 + -propylbenzene are rather complex, and are described in detail below.
This substance is in the atmosphere, because it is volatile to a certain extent, or may participate in photochemical reactions. If it escapes into the atmosphere, it will react with active substances such as hydroxyl radicals under conditions such as light. This reaction may generate a series of secondary pollutants, such as ozone. If the concentration of ozone is abnormally high, it will cause a decrease in air quality, which not only affects visibility, but also irritates the human respiratory tract and can cause symptoms such as cough and asthma.
As for the water environment, if it enters rivers, lakes and seas and other waters, due to its own chemical characteristics, it may be insoluble in water, partially or floating on the water surface, hindering the gas exchange between the water body and the atmosphere, and affecting the dissolved oxygen content in the water. And it also poses a potential threat to aquatic organisms, or is ingested by aquatic organisms, accumulates in the body of organisms, interferes with the normal physiological metabolism of organisms, causing their growth and reproduction to be hindered, and even causes the death of organisms, thereby destroying the balance of aquatic ecosystems.
In terms of soil environment, after entering the soil, it is relatively stable due to its chemical structure, degrades or is relatively slow. or adsorbed on the surface of soil particles, changes the soil physical and chemical properties, affects the soil pore structure and aeration, and hinders the absorption of water and nutrients by plant roots. If this substance is absorbed by plants or accumulated in plants, it will be transmitted through the food chain, which will have toxic effects on high trophic organisms and threaten the ecosystem and human health.
In summary, 1 + -alkane-5 + -ene-2 + -methyl-4 + -propylbenzene has many potential adverse effects on the atmosphere, water and soil environment. Its production, use and discharge process should be carefully controlled to reduce its harm to the environment.
This substance is in the atmosphere, because it is volatile to a certain extent, or may participate in photochemical reactions. If it escapes into the atmosphere, it will react with active substances such as hydroxyl radicals under conditions such as light. This reaction may generate a series of secondary pollutants, such as ozone. If the concentration of ozone is abnormally high, it will cause a decrease in air quality, which not only affects visibility, but also irritates the human respiratory tract and can cause symptoms such as cough and asthma.
As for the water environment, if it enters rivers, lakes and seas and other waters, due to its own chemical characteristics, it may be insoluble in water, partially or floating on the water surface, hindering the gas exchange between the water body and the atmosphere, and affecting the dissolved oxygen content in the water. And it also poses a potential threat to aquatic organisms, or is ingested by aquatic organisms, accumulates in the body of organisms, interferes with the normal physiological metabolism of organisms, causing their growth and reproduction to be hindered, and even causes the death of organisms, thereby destroying the balance of aquatic ecosystems.
In terms of soil environment, after entering the soil, it is relatively stable due to its chemical structure, degrades or is relatively slow. or adsorbed on the surface of soil particles, changes the soil physical and chemical properties, affects the soil pore structure and aeration, and hinders the absorption of water and nutrients by plant roots. If this substance is absorbed by plants or accumulated in plants, it will be transmitted through the food chain, which will have toxic effects on high trophic organisms and threaten the ecosystem and human health.
In summary, 1 + -alkane-5 + -ene-2 + -methyl-4 + -propylbenzene has many potential adverse effects on the atmosphere, water and soil environment. Its production, use and discharge process should be carefully controlled to reduce its harm to the environment.
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