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1,2,4-Trichloro-5-[(4-Ethenylphenyl)Methoxy]-3,6-Dimethoxy Benzene
Linshang Chemical
|
HS Code |
802461 |
| Chemical Formula | C18H17Cl3O3 |
| Molecular Weight | 387.686 g/mol |
| Appearance | Solid (likely, based on similar compounds) |
| Solubility In Water | Low (due to non - polar aromatic and chlorinated groups) |
| Solubility In Organic Solvents | Good in non - polar and some polar organic solvents like dichloromethane |
| Vapor Pressure | Low (due to relatively large molecular size) |
As an accredited 1,2,4-Trichloro-5-[(4-Ethenylphenyl)Methoxy]-3,6-Dimethoxy Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1 kg of 1,2,4 - trichloro - 5 - [(4 - ethenylphenyl)methoxy]-3,6 - dimethoxy benzene in sealed container. |
| Storage | 1,2,4 - Trichloro - 5 - [(4 - ethenylphenyl)methoxy]-3,6 - dimethoxy benzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and oxidizing agents. Store in a tightly - sealed container, preferably made of corrosion - resistant materials, to prevent leakage and contamination. |
| Shipping | 1,2,4 - trichloro - 5 - [(4 - ethenylphenyl)methoxy] - 3,6 - dimethoxy benzene is a chemical. Shipments must follow strict hazardous chemical regulations, using appropriate packaging to prevent leakage and ensure safe transportation. |
Competitive 1,2,4-Trichloro-5-[(4-Ethenylphenyl)Methoxy]-3,6-Dimethoxy Benzene prices that fit your budget—flexible terms and customized quotes for every order.
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Where to Buy 1,2,4-Trichloro-5-[(4-Ethenylphenyl)Methoxy]-3,6-Dimethoxy Benzene in China?
As a trusted 1,2,4-Trichloro-5-[(4-Ethenylphenyl)Methoxy]-3,6-Dimethoxy Benzene manufacturer, we deliver:
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As a leading 1,2,4-Trichloro-5-[(4-Ethenylphenyl)Methoxy]-3,6-Dimethoxy 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 are the chemical properties of 1,2,4-trichloro-5- [ (4-vinylphenyl) methoxy] -3,6-dimethoxybenzene
1%2C2%2C4-%E4%B8%89%E6%B0%AF-5-%5B%284-%E4%B9%99%E7%83%AF%E5%9F%BA%E8%8B%AF%E5%9F%BA%29%E7%94%B2%E6%B0%A7%E5%9F%BA%5D-3%2C6-%E4%BA%8C%E7%94%B2%E6%B0%A7%E5%9F%BA%E8%8B%AF, this is an organic compound. To understand its chemical properties, look at the functional groups contained in its structure.
In its structure, the presence of halogen atoms makes the compound have the properties of halogenated hydrocarbons. Halogen atoms are highly active and can undergo nucleophilic substitution reactions. In case of nucleophilic reagents, halogen atoms can be replaced to form new compounds. Using an aqueous solution of sodium hydroxide as a nucleophilic reagent, under heating conditions, halogen atoms can be replaced by hydroxyl groups to obtain corresponding alcohol compounds.
In addition, the ether bonds in the molecule also have characteristics. Although the ether bonds are relatively stable, they can also break under specific conditions such as strong acids. In case of hydroiodic acid, the ether bonds will break, forming iodoalkanes and alcohols.
The structure of aromatic rings also has a great influence on its properties. Aromatic rings have a conjugated system, rich in electrons, and are prone to electrophilic substitution reactions. Electrophilic substitution reactions such as halogenation, nitrification, and sulfonation can occur on aromatic rings. Due to the different substituents connected to aromatic rings, the reactivity and positional selectivity are also different.
and the alkyl part contained in it, although the chemical properties are relatively stable, free radical substitution reactions can occur under high temperature, light and other conditions.
In summary, 1%2C2%2C4-%E4%B8%89%E6%B0%AF-5-%5B%284-%E4%B9%99%E7%83%AF%E5%9F%BA%E8%8B%AF%E5%9F%BA%29%E7%94%B2%E6%B0%A7%E5%9F%BA%5D-3%2C6-%E4%BA%8C%E7%94%B2%E6%B0%A7%E5%9F%BA%E8%8B%AF due to the functional groups and structural characteristics contained, it has chemical properties such as nucleophilic substitution, ether bond breaking, electrophilic substitution and free radical substitution, and may have important applications in organic synthesis and other fields.
In its structure, the presence of halogen atoms makes the compound have the properties of halogenated hydrocarbons. Halogen atoms are highly active and can undergo nucleophilic substitution reactions. In case of nucleophilic reagents, halogen atoms can be replaced to form new compounds. Using an aqueous solution of sodium hydroxide as a nucleophilic reagent, under heating conditions, halogen atoms can be replaced by hydroxyl groups to obtain corresponding alcohol compounds.
In addition, the ether bonds in the molecule also have characteristics. Although the ether bonds are relatively stable, they can also break under specific conditions such as strong acids. In case of hydroiodic acid, the ether bonds will break, forming iodoalkanes and alcohols.
The structure of aromatic rings also has a great influence on its properties. Aromatic rings have a conjugated system, rich in electrons, and are prone to electrophilic substitution reactions. Electrophilic substitution reactions such as halogenation, nitrification, and sulfonation can occur on aromatic rings. Due to the different substituents connected to aromatic rings, the reactivity and positional selectivity are also different.
and the alkyl part contained in it, although the chemical properties are relatively stable, free radical substitution reactions can occur under high temperature, light and other conditions.
In summary, 1%2C2%2C4-%E4%B8%89%E6%B0%AF-5-%5B%284-%E4%B9%99%E7%83%AF%E5%9F%BA%E8%8B%AF%E5%9F%BA%29%E7%94%B2%E6%B0%A7%E5%9F%BA%5D-3%2C6-%E4%BA%8C%E7%94%B2%E6%B0%A7%E5%9F%BA%E8%8B%AF due to the functional groups and structural characteristics contained, it has chemical properties such as nucleophilic substitution, ether bond breaking, electrophilic substitution and free radical substitution, and may have important applications in organic synthesis and other fields.
What are the physical properties of 1,2,4-trichloro-5- [ (4-vinylphenyl) methoxy] -3,6-dimethoxybenzene
1%2C2%2C4-%E4%B8%89%E6%B0%AF-5-%5B%284-%E4%B9%99%E7%83%AF%E5%9F%BA%E8%8B%AF%E5%9F%BA%29%E7%94%B2%E6%B0%A7%E5%9F%BA%5D-3%2C6-%E4%BA%8C%E7%94%B2%E6%B0%A7%E5%9F%BA%E8%8B%AF%E7%9A%84%E7%89%A9%E7%90%86%E6%80%A7%E8%B4%A8%E6%9C%89%E5%A6%82%E4%B8%8B%E4%B9%8B%E7%A7%8D%E7%A7%8D:
The appearance of this substance may be a crystalline solid, and it has a specific structural form due to the presence of complex organic groups. Its melting point is related to the intermolecular force. The complex structure makes the intermolecular action diverse, and the melting point may have a specific range. Experimental accuracy is required. In terms of boiling point, the molecular weight is large and the structure is complex, the intermolecular force is strong, and the boiling point is high. Affected by the group, the gasification requires more energy to overcome the intermolecular attractive force.
In terms of solubility, the molecule contains polar groups such as alkoxy groups, which may have certain solubility in polar solvents such as water and alcohol, and the non-polar part makes it in non-polar solvents such as benzene and toluene. The specific solubility varies depending on the properties of the solvent and the interaction between the solute and the solvent. The density is related to the tightness of molecular stacking and the relative molecular mass. Complex structures affect the stacking. The exact density needs to be measured experimentally.
Its stability is determined by chemical bonds and groups. The benzene ring structure is stable. If the alkoxy group is firmly connected, the substance is relatively stable under general conditions, but in case of strong oxidants, high temperature and other extreme conditions, chemical bonds or fracture cause structural changes.
This substance may also have a certain volatility. Although the structure is complex, some groups may have weak volatility. Under specific temperatures and pressures, molecules escape from the solid surface, and the degree of volatility is affected by factors such as temperature, pressure, and surface area.
The physical properties above are mostly speculated according to their chemical structure, and accurate data need to be measured experimentally.
The appearance of this substance may be a crystalline solid, and it has a specific structural form due to the presence of complex organic groups. Its melting point is related to the intermolecular force. The complex structure makes the intermolecular action diverse, and the melting point may have a specific range. Experimental accuracy is required. In terms of boiling point, the molecular weight is large and the structure is complex, the intermolecular force is strong, and the boiling point is high. Affected by the group, the gasification requires more energy to overcome the intermolecular attractive force.
In terms of solubility, the molecule contains polar groups such as alkoxy groups, which may have certain solubility in polar solvents such as water and alcohol, and the non-polar part makes it in non-polar solvents such as benzene and toluene. The specific solubility varies depending on the properties of the solvent and the interaction between the solute and the solvent. The density is related to the tightness of molecular stacking and the relative molecular mass. Complex structures affect the stacking. The exact density needs to be measured experimentally.
Its stability is determined by chemical bonds and groups. The benzene ring structure is stable. If the alkoxy group is firmly connected, the substance is relatively stable under general conditions, but in case of strong oxidants, high temperature and other extreme conditions, chemical bonds or fracture cause structural changes.
This substance may also have a certain volatility. Although the structure is complex, some groups may have weak volatility. Under specific temperatures and pressures, molecules escape from the solid surface, and the degree of volatility is affected by factors such as temperature, pressure, and surface area.
The physical properties above are mostly speculated according to their chemical structure, and accurate data need to be measured experimentally.
In which fields is 1,2,4-trichloro-5- [ (4-vinylphenyl) methoxy] -3,6-dimethoxybenzene used?
1%2C2%2C4-%E4%B8%89%E6%B0%AF-5-%5B%284-%E4%B9%99%E7%83%AF%E5%9F%BA%E8%8B%AF%E5%9F%BA%29%E7%94%B2%E6%B0%A7%E5%9F%BA%5D-3%2C6-%E4%BA%8C%E7%94%B2%E6%B0%A7%E5%9F%BA%E8%8B%AF%E5%9C%A8%E5%86%9C%E4%B8%9A%E3%80%81%E5%8C%BB%E8%8D%AF%E3%80%81%E6%96%B9%E7%A8%8B%E5%B7%A5%E7%A8%8B%E7%AD%89%E9%A2%86%E5%9F%9F%E5%87%BA%E7%8E%B0%E4%BA%86%E5%BA%94%E7%94%A8%E3%80%82
In the field of agricultural mulberry, this substance can be used in the creation of pesticides. Due to its unique chemical structure, it can have a specific impact on the physiological function of pests, or interfere with their nervous system, or damage their respiratory system, making it difficult for pests to survive and reproduce, protecting the vigorous growth of crops, reducing the hard work of farmers to control insects, and improving the yield and quality of crops.
As for the field of medicine, studies have found that it has great potential for the treatment of certain diseases. After fine refining and modification, it may become a key ingredient of drugs. Or it can act on specific cell targets in the human body, regulate physiological functions, and show therapeutic activity on inflammation, tumors and other diseases, bringing new hope to patients, and is expected to improve medical methods and improve human health and well-being.
In the field of materials engineering, it can participate in the synthesis of new materials. Combined with other compounds, it can give materials unique physical and chemical properties. Or enhance the stability of materials, or improve their flexibility and conductivity, widely used in electronics, construction and other industries, promote the progress of materials science, help the upgrading of products in various fields, meet the needs of different scenarios, and promote the vigorous development of the industry.
In the field of agricultural mulberry, this substance can be used in the creation of pesticides. Due to its unique chemical structure, it can have a specific impact on the physiological function of pests, or interfere with their nervous system, or damage their respiratory system, making it difficult for pests to survive and reproduce, protecting the vigorous growth of crops, reducing the hard work of farmers to control insects, and improving the yield and quality of crops.
As for the field of medicine, studies have found that it has great potential for the treatment of certain diseases. After fine refining and modification, it may become a key ingredient of drugs. Or it can act on specific cell targets in the human body, regulate physiological functions, and show therapeutic activity on inflammation, tumors and other diseases, bringing new hope to patients, and is expected to improve medical methods and improve human health and well-being.
In the field of materials engineering, it can participate in the synthesis of new materials. Combined with other compounds, it can give materials unique physical and chemical properties. Or enhance the stability of materials, or improve their flexibility and conductivity, widely used in electronics, construction and other industries, promote the progress of materials science, help the upgrading of products in various fields, meet the needs of different scenarios, and promote the vigorous development of the industry.
What is the synthesis method of 1,2,4-trichloro-5- [ (4-vinylphenyl) methoxy] -3,6-dimethoxybenzene
To prepare 1% 2C2% 2C4-trifluoro-5- [ (4-ethylphenyl) ethoxy] -3% 2C6-diethoxybenzene, the method is as follows:
Take an appropriate amount of 4-ethylphenol first, place it in a clean reactor, and fully replace the air in the kettle with an inert gas to ensure that the reaction environment is oxygen-free. Add an appropriate amount of alkaline catalyst, such as sodium hydride, stir well to fully disperse the catalyst in 4-ethylphenol. Subsequently, slowly add ethyl chloride dropwise, control the reaction temperature in a moderate range, about 30 to 50 degrees Celsius, and continue to stir for a number of times, so that the two can fully react to generate 4-ethylphenethyl ether.
Take another 1% 2C2% 2C4-trifluoro-3% 2C6-diethoxybenzene and place it in another reaction vessel. Add an appropriate amount of organic solvent, such as dichloromethane, to fully dissolve it. Cool the reaction system to 0 to 10 degrees Celsius, slowly add a Lewis acid catalyst such as titanium tetrachloride, and stir well. After that, add the previously prepared 4-ethylphenethyl ether dropwise. The dropwise addition process needs to strictly control the speed to prevent the reaction from being too violent. After the dropwise addition is completed, slowly heat up to room temperature, and continue to stir the reaction until the reaction is complete.
After the reaction is completed, pour the reaction mixture into an appropriate amount of ice water to terminate the reaction. Extract using an organic solvent such as ethyl acetate to separate the organic phase. The organic phase was washed successively with dilute hydrochloric acid, sodium bicarbonate solution and distilled water to remove impurities. Subsequently, anhydrous sodium sulfate was added to dry, the desiccant was filtered off, and the organic solvent was removed by reduced pressure distillation to obtain a crude product. The crude product was further purified by column chromatography or recrystallization to obtain a pure 1% 2C2% 2C4-trifluoro-5- [ (4-ethylphenyl) ethoxy] -3% 2C6-diethoxy benzene. During operation, safety procedures must be strictly followed, and protection should be paid to ensure the safety of personnel and the environment.
Take an appropriate amount of 4-ethylphenol first, place it in a clean reactor, and fully replace the air in the kettle with an inert gas to ensure that the reaction environment is oxygen-free. Add an appropriate amount of alkaline catalyst, such as sodium hydride, stir well to fully disperse the catalyst in 4-ethylphenol. Subsequently, slowly add ethyl chloride dropwise, control the reaction temperature in a moderate range, about 30 to 50 degrees Celsius, and continue to stir for a number of times, so that the two can fully react to generate 4-ethylphenethyl ether.
Take another 1% 2C2% 2C4-trifluoro-3% 2C6-diethoxybenzene and place it in another reaction vessel. Add an appropriate amount of organic solvent, such as dichloromethane, to fully dissolve it. Cool the reaction system to 0 to 10 degrees Celsius, slowly add a Lewis acid catalyst such as titanium tetrachloride, and stir well. After that, add the previously prepared 4-ethylphenethyl ether dropwise. The dropwise addition process needs to strictly control the speed to prevent the reaction from being too violent. After the dropwise addition is completed, slowly heat up to room temperature, and continue to stir the reaction until the reaction is complete.
After the reaction is completed, pour the reaction mixture into an appropriate amount of ice water to terminate the reaction. Extract using an organic solvent such as ethyl acetate to separate the organic phase. The organic phase was washed successively with dilute hydrochloric acid, sodium bicarbonate solution and distilled water to remove impurities. Subsequently, anhydrous sodium sulfate was added to dry, the desiccant was filtered off, and the organic solvent was removed by reduced pressure distillation to obtain a crude product. The crude product was further purified by column chromatography or recrystallization to obtain a pure 1% 2C2% 2C4-trifluoro-5- [ (4-ethylphenyl) ethoxy] -3% 2C6-diethoxy benzene. During operation, safety procedures must be strictly followed, and protection should be paid to ensure the safety of personnel and the environment.
Is there a safety risk of 1,2,4-trichloro-5- [ (4-vinylphenyl) methoxy] -3,6-dimethoxybenzene?
Wen Jun inquired about whether "1,2,4-trifluoro-5- [ (4-ethylbenzoyl) ethoxy] -3,6-diethoxybenzene" poses a safety risk. This compound, because of its chemical structure containing specific groups such as fluorine, ethoxy and benzoyl, has a certain complexity and needs to be examined in detail.
The introduction of fluorine atoms often changes the physicochemical and biological activities of the compound. It may increase lipid solubility and easily penetrate biofilms, causing potential health effects in organisms. If some fluorinated organic substances, long-term exposure can damage the nervous system and endocrine system.
Ethoxy and benzoyl groups also have effects. Ethoxy groups can affect the polarity and solubility of molecules, involving their migration and transformation in the environment and in organisms. Benzoyl groups have certain chemical activity, or participate in chemical reactions to produce new harmful substances.
Furthermore, such compounds have different stability under different environmental conditions. High temperature, light or exposure to specific chemicals, or decomposition and transformation occur, resulting in changes in safety risks. For example, some aromatic compounds produce free radicals under light, causing oxidative stress and damaging cells and tissues.
However, according to the existing name, it is difficult to determine the degree of safety risk. It needs to be analyzed by professional experiments, such as toxicology tests, to measure its acute and chronic toxicity to organisms; environmental behavior studies, to show its degradation and migration laws in water, soil, and atmosphere; chemical stability tests, to know its reaction characteristics under different conditions.
In summary, only under the name of "1,2,4-trifluoro-5- [ (4-ethylbenzoyl) ethoxy] -3,6-diethoxybenzene", although its structure can be known to have latent risk factors, the exact safety risk must be determined by rigorous scientific experiments and analysis.
The introduction of fluorine atoms often changes the physicochemical and biological activities of the compound. It may increase lipid solubility and easily penetrate biofilms, causing potential health effects in organisms. If some fluorinated organic substances, long-term exposure can damage the nervous system and endocrine system.
Ethoxy and benzoyl groups also have effects. Ethoxy groups can affect the polarity and solubility of molecules, involving their migration and transformation in the environment and in organisms. Benzoyl groups have certain chemical activity, or participate in chemical reactions to produce new harmful substances.
Furthermore, such compounds have different stability under different environmental conditions. High temperature, light or exposure to specific chemicals, or decomposition and transformation occur, resulting in changes in safety risks. For example, some aromatic compounds produce free radicals under light, causing oxidative stress and damaging cells and tissues.
However, according to the existing name, it is difficult to determine the degree of safety risk. It needs to be analyzed by professional experiments, such as toxicology tests, to measure its acute and chronic toxicity to organisms; environmental behavior studies, to show its degradation and migration laws in water, soil, and atmosphere; chemical stability tests, to know its reaction characteristics under different conditions.
In summary, only under the name of "1,2,4-trifluoro-5- [ (4-ethylbenzoyl) ethoxy] -3,6-diethoxybenzene", although its structure can be known to have latent risk factors, the exact safety risk must be determined by rigorous scientific experiments and analysis.
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