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1-(Chloromethyl)-4-Phenoxybenzene
Linshang Chemical
|
HS Code |
892631 |
| Chemical Formula | C13H11ClO |
| Molecular Weight | 218.68 |
| Appearance | Solid (usually white or off - white) |
| Boiling Point | Approximately 320 - 330 °C |
| Melting Point | 62 - 64 °C |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in many organic solvents like dichloromethane, toluene |
| Odor | May have a characteristic aromatic odor |
| Flash Point | Approximately 147 °C |
| Vapor Pressure | Low |
As an accredited 1-(Chloromethyl)-4-Phenoxybenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 1-(chloromethyl)-4 - phenoxybenzene packaged in a sealed chemical - grade bottle. |
| Storage | 1-(Chloromethyl)-4 - phenoxybenzene should be stored in a cool, dry, well - ventilated area, away from heat sources and ignition sources. Keep it in a tightly sealed container to prevent leakage. Store it separately from oxidizing agents, bases, and other reactive substances to avoid potential chemical reactions. Label the storage container clearly for easy identification. |
| Shipping | 1-(Chloromethyl)-4 -phenoxybenzene is a chemical. Shipping requires compliance with regulations for hazardous chemicals. It should be properly packaged in suitable containers, labeled clearly, and transported by carriers licensed for such substances. |
Competitive 1-(Chloromethyl)-4-Phenoxybenzene prices that fit your budget—flexible terms and customized quotes for every order.
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What are the main uses of 1- (chloromethyl) -4-phenoxybenzene?
1 - (cyanomethyl) - 4 -phenoxybenzene, its main uses are as follows:
This compound is widely used in the field of organic synthesis. In the field of medicinal chemistry, it is often used as a key intermediate. Due to its unique chemical structure, it can participate in many reactions and help build complex drug molecular structures. In the process of developing many new drugs, structural modification and derivatization operations can be carried out on this basis to obtain compounds with specific biological activities, which are expected to be used in the treatment of diseases. For example, for some difficult diseases, drugs based on this structure can be cleverly designed, which may bring good news to patients.
In the field of materials science, it is also of great significance. It can be used to prepare polymer materials with special properties. By introducing it into the polymer chain segment, the material can be imparted with excellent thermal stability, mechanical properties or optical properties. For example, in the preparation of some high-end electronic materials, the addition of an appropriate amount of this compound can optimize the electrical properties of the material, improve the stability and reliability of electronic components, and meet the stringent requirements of modern electronic technology for high-performance materials.
In pesticide chemistry, 1- (cyanomethyl) -4-phenoxy benzene is also used. It can be used as an important raw material for the synthesis of high-efficiency and low-toxicity pesticides. With the help of the optimization of its structure, targeted pesticides can be developed to precisely target pests, effectively control pests and diseases, while reducing the impact on the environment and non-target organisms, in line with the current trend of green agriculture development, and contribute to the sustainable development of agriculture.
This compound is widely used in the field of organic synthesis. In the field of medicinal chemistry, it is often used as a key intermediate. Due to its unique chemical structure, it can participate in many reactions and help build complex drug molecular structures. In the process of developing many new drugs, structural modification and derivatization operations can be carried out on this basis to obtain compounds with specific biological activities, which are expected to be used in the treatment of diseases. For example, for some difficult diseases, drugs based on this structure can be cleverly designed, which may bring good news to patients.
In the field of materials science, it is also of great significance. It can be used to prepare polymer materials with special properties. By introducing it into the polymer chain segment, the material can be imparted with excellent thermal stability, mechanical properties or optical properties. For example, in the preparation of some high-end electronic materials, the addition of an appropriate amount of this compound can optimize the electrical properties of the material, improve the stability and reliability of electronic components, and meet the stringent requirements of modern electronic technology for high-performance materials.
In pesticide chemistry, 1- (cyanomethyl) -4-phenoxy benzene is also used. It can be used as an important raw material for the synthesis of high-efficiency and low-toxicity pesticides. With the help of the optimization of its structure, targeted pesticides can be developed to precisely target pests, effectively control pests and diseases, while reducing the impact on the environment and non-target organisms, in line with the current trend of green agriculture development, and contribute to the sustainable development of agriculture.
What are the physical properties of 1- (chloromethyl) -4-phenoxybenzene?
(1) Halomethyl-4 -pyridyl pyridine, which is an organic compound. It has the following physical properties:
1. ** Appearance properties **: Under normal conditions, halomethyl-4 -pyridyl pyridine is mostly white to light yellow crystalline powder. This color state is conducive to preliminary identification and observation by the naked eye in many chemical experiments and industrial production scenarios.
2. ** Melting point **: Its melting point is within a specific range, and the exact melting point value will vary depending on the type of halogen atom and the specific structure. Melting point, as an important physical property of a substance, is of great significance for determining the purity of the compound and performing related separation and purification operations. In the post-processing process of chemical synthesis, the purity of the product can be evaluated by measuring the melting point. If the melting point is consistent with the theoretical value and the melting range is narrow, the purity of the product is often characterized.
3. ** Solubility **: In common organic solvents, halomethyl-4-pyridyl pyridine exhibits certain solubility properties. Usually, it is soluble in some polar organic solvents, such as methanol, ethanol, dichloromethane, etc. This solubility property facilitates its use as a reactant or intermediate in organic synthesis reactions. Since most organic reactions are carried out in solution systems, good solubility ensures that the reactants are fully contacted and mixed, thereby accelerating the reaction process and improving the reaction efficiency.
4. ** Stability **: The compound has certain chemical stability under conventional conditions, but its structure may change under specific conditions, such as high temperature, strong acid-base environment or specific oxidants and reducing agents. When storing and using, these factors should be fully considered to properly preserve and use this compound rationally to avoid deterioration or accidental chemical reactions due to improper conditions.
1. ** Appearance properties **: Under normal conditions, halomethyl-4 -pyridyl pyridine is mostly white to light yellow crystalline powder. This color state is conducive to preliminary identification and observation by the naked eye in many chemical experiments and industrial production scenarios.
2. ** Melting point **: Its melting point is within a specific range, and the exact melting point value will vary depending on the type of halogen atom and the specific structure. Melting point, as an important physical property of a substance, is of great significance for determining the purity of the compound and performing related separation and purification operations. In the post-processing process of chemical synthesis, the purity of the product can be evaluated by measuring the melting point. If the melting point is consistent with the theoretical value and the melting range is narrow, the purity of the product is often characterized.
3. ** Solubility **: In common organic solvents, halomethyl-4-pyridyl pyridine exhibits certain solubility properties. Usually, it is soluble in some polar organic solvents, such as methanol, ethanol, dichloromethane, etc. This solubility property facilitates its use as a reactant or intermediate in organic synthesis reactions. Since most organic reactions are carried out in solution systems, good solubility ensures that the reactants are fully contacted and mixed, thereby accelerating the reaction process and improving the reaction efficiency.
4. ** Stability **: The compound has certain chemical stability under conventional conditions, but its structure may change under specific conditions, such as high temperature, strong acid-base environment or specific oxidants and reducing agents. When storing and using, these factors should be fully considered to properly preserve and use this compound rationally to avoid deterioration or accidental chemical reactions due to improper conditions.
What are the chemical properties of 1- (chloromethyl) -4-phenoxybenzene?
1 - (cyanomethyl) - 4 - phenoxybenzene, this is an organic compound. Its chemical properties are quite rich and of great research value.
When it comes to stability, under normal temperature and pressure, if there are no special conditions or reagents, its structure is relatively stable and can be stored for a long time. In case of hot topics, open flames or strong oxidants, it is potentially dangerous and may cause combustion and explosion.
In terms of solubility, this compound is slightly lipophilic. It has a certain solubility in common organic solvents such as ethanol, ether, and chloroform, but it has little solubility in water. This property makes it possible to achieve the corresponding purpose by selecting a suitable solvent in the process of organic synthesis and separation and purification.
Reactive activity is also considerable. Its benzene ring structure endows it with aromatic properties and can participate in many electrophilic substitution reactions. In the case of halogenating agents, halogenation reactions can occur, and halogen atoms replace hydrogen atoms on the benzene ring; in the case of nitrifying reagents, nitrification reactions can also be carried out, introducing nitro groups on the benzene ring. The cyanogen methyl part can undergo hydrolysis and be converted into carboxyl groups under the catalysis of acids or bases; it can also undergo nucleophilic addition reactions with nucleophiles to expand the structure of molecules. As for the phenoxy group, because of its lone pair of electrons in the oxygen atom, it can be used as an electron donor to participate in some reactions involving electron transfer and enhance the reactivity of the molecule.
In addition, the chemical properties of the compound are also affected by the electronic and spatial effects of its surrounding substituents. Different substituents can change the distribution of the electron cloud in the molecule, which in turn has a significant effect on its reaction check point and reactivity.
When it comes to stability, under normal temperature and pressure, if there are no special conditions or reagents, its structure is relatively stable and can be stored for a long time. In case of hot topics, open flames or strong oxidants, it is potentially dangerous and may cause combustion and explosion.
In terms of solubility, this compound is slightly lipophilic. It has a certain solubility in common organic solvents such as ethanol, ether, and chloroform, but it has little solubility in water. This property makes it possible to achieve the corresponding purpose by selecting a suitable solvent in the process of organic synthesis and separation and purification.
Reactive activity is also considerable. Its benzene ring structure endows it with aromatic properties and can participate in many electrophilic substitution reactions. In the case of halogenating agents, halogenation reactions can occur, and halogen atoms replace hydrogen atoms on the benzene ring; in the case of nitrifying reagents, nitrification reactions can also be carried out, introducing nitro groups on the benzene ring. The cyanogen methyl part can undergo hydrolysis and be converted into carboxyl groups under the catalysis of acids or bases; it can also undergo nucleophilic addition reactions with nucleophiles to expand the structure of molecules. As for the phenoxy group, because of its lone pair of electrons in the oxygen atom, it can be used as an electron donor to participate in some reactions involving electron transfer and enhance the reactivity of the molecule.
In addition, the chemical properties of the compound are also affected by the electronic and spatial effects of its surrounding substituents. Different substituents can change the distribution of the electron cloud in the molecule, which in turn has a significant effect on its reaction check point and reactivity.
What are the precautions for the synthesis of 1- (chloromethyl) -4-phenoxybenzene?
(1) Preparation of raw materials
If you want to make 1- (cyanomethyl) -4-phenoxy benzene, you should first choose the raw materials carefully. Cyanomethyl related reagents must be pure and free of impurities. If they contain impurities, the reaction will go wrong and the product will be impure. The raw materials of phenoxy benzene must also be carefully selected, and their purity is related to the success or failure of the reaction and the quality of the product. And the storage of various reagents depends on their nature, avoiding moisture, light, and heat to prevent deterioration.
(2) Control of reaction conditions
1. The temperature is extremely high. This reaction is smooth only in a specific temperature range. If the temperature is too low, the reaction is slow, time-consuming and the yield is not high; if the temperature is too high, the side reactions will be plentiful, and the products will be complicated and difficult to analyze. Therefore, during the reaction, precise temperature control devices should be used, such as constant temperature baths, temperature controllers, etc., to ensure that the temperature of the reaction system is constant in a suitable range.
2. Pressure cannot be ignored either. Some steps may require a specific pressure environment, or normal pressure, or pressurization. Improper pressure can disturb the reaction rate and direction. Taking a high-pressure reaction as an example, a pressure-resistant device must be used, and pressure changes must be closely monitored to prevent accidents.
3. The reaction time must be checked. If it is too short, the reaction will not be completed, and the amount of product will be small; if it is too long, it will consume resources, and the product may be degraded At the beginning of the experiment, it is advisable to do a pre-exploration test to determine the optimal reaction time.
(3) The care of operation
1. Mix the reagents, and the action should be slow and uniform. With a stirring device, slowly mix the reagents to make the reaction check points evenly distributed, avoiding local overheating or uneven reaction.
2. During the reaction, closely observe the changes of the system, such as color, bubbles, precipitation, etc. This is a sign of the reaction process. If there is any abnormality, quickly check the cause, adjust the conditions, or stop the reaction.
3. Separation and purification are the keys to obtaining pure products. According to the physical properties of the product and impurities, the selection method is appropriate, such as distillation, extraction, recrystallization, etc. During the operation, follow the rules and strive to minimize the loss of the product and achieve the highest purity.
In short, the production of 1- (cyanomethyl) -4-phenoxy benzene requires all links to be interconnected, and care must be taken to obtain satisfactory results.
If you want to make 1- (cyanomethyl) -4-phenoxy benzene, you should first choose the raw materials carefully. Cyanomethyl related reagents must be pure and free of impurities. If they contain impurities, the reaction will go wrong and the product will be impure. The raw materials of phenoxy benzene must also be carefully selected, and their purity is related to the success or failure of the reaction and the quality of the product. And the storage of various reagents depends on their nature, avoiding moisture, light, and heat to prevent deterioration.
(2) Control of reaction conditions
1. The temperature is extremely high. This reaction is smooth only in a specific temperature range. If the temperature is too low, the reaction is slow, time-consuming and the yield is not high; if the temperature is too high, the side reactions will be plentiful, and the products will be complicated and difficult to analyze. Therefore, during the reaction, precise temperature control devices should be used, such as constant temperature baths, temperature controllers, etc., to ensure that the temperature of the reaction system is constant in a suitable range.
2. Pressure cannot be ignored either. Some steps may require a specific pressure environment, or normal pressure, or pressurization. Improper pressure can disturb the reaction rate and direction. Taking a high-pressure reaction as an example, a pressure-resistant device must be used, and pressure changes must be closely monitored to prevent accidents.
3. The reaction time must be checked. If it is too short, the reaction will not be completed, and the amount of product will be small; if it is too long, it will consume resources, and the product may be degraded At the beginning of the experiment, it is advisable to do a pre-exploration test to determine the optimal reaction time.
(3) The care of operation
1. Mix the reagents, and the action should be slow and uniform. With a stirring device, slowly mix the reagents to make the reaction check points evenly distributed, avoiding local overheating or uneven reaction.
2. During the reaction, closely observe the changes of the system, such as color, bubbles, precipitation, etc. This is a sign of the reaction process. If there is any abnormality, quickly check the cause, adjust the conditions, or stop the reaction.
3. Separation and purification are the keys to obtaining pure products. According to the physical properties of the product and impurities, the selection method is appropriate, such as distillation, extraction, recrystallization, etc. During the operation, follow the rules and strive to minimize the loss of the product and achieve the highest purity.
In short, the production of 1- (cyanomethyl) -4-phenoxy benzene requires all links to be interconnected, and care must be taken to obtain satisfactory results.
What are the environmental effects of 1- (chloromethyl) -4-phenoxybenzene?
(1) Gas methyl substances and tetrahydroxyphenyl phenols, both of which have a significant impact on the environment.
Gas methyl substances are commonly found in chemical processes and various materials. If they escape into the atmosphere, they can be related to photochemical reactions. Gas methyl substances can participate in complex photochemical reactions. Under sunlight, they interact with other components in the atmosphere, such as nitrogen oxides. This reaction may cause the formation of secondary pollutants such as ozone. If the ozone concentration rises near the ground, it will endanger human health and make people feel uncomfortable breathing, especially for people with fragile respiratory tracts, such as the elderly, children and people with respiratory diseases. And when the air armor stays in the atmosphere, or migrates with the air flow, it affects the regional air quality, and causes severe weather conditions such as smog.
As for tetrahydroxyphenyl phenol, it also has a significant effect in the environment. If it flows into the water body, the impact on aquatic organisms should not be underestimated. This substance may have certain toxicity and can interfere with the physiological function of aquatic organisms. If it affects the reproductive system of fish, it will reduce their reproductive ability, reduce the hatching rate of fish eggs, and increase the deformity rate of juvenile fish. In the food chain, tetrahydroxyphenyl phenol can be transmitted and accumulated along the food chain due to biological enrichment. After lower aquatic organisms ingest this substance, although the concentration is low or low, through predation, the accumulated concentration in the organisms at the top of the food chain gradually increases, which eventually affects the balance of the entire aquatic ecosystem. At the same time, if the soil is polluted by it, or the soil microbial community structure is changed, which affects the soil nutrient cycle and material transformation, it is also unfavorable to plant growth, resulting in plant dysplasia and reduced yield.
Therefore, gas methyl and tetrahydroxyphenyl phenols have a wide and far-reaching impact on the environment. It is necessary to pay attention to it, control its discharge, and prevent it from polluting the environment, so as to maintain ecological balance and human well-being.
Gas methyl substances are commonly found in chemical processes and various materials. If they escape into the atmosphere, they can be related to photochemical reactions. Gas methyl substances can participate in complex photochemical reactions. Under sunlight, they interact with other components in the atmosphere, such as nitrogen oxides. This reaction may cause the formation of secondary pollutants such as ozone. If the ozone concentration rises near the ground, it will endanger human health and make people feel uncomfortable breathing, especially for people with fragile respiratory tracts, such as the elderly, children and people with respiratory diseases. And when the air armor stays in the atmosphere, or migrates with the air flow, it affects the regional air quality, and causes severe weather conditions such as smog.
As for tetrahydroxyphenyl phenol, it also has a significant effect in the environment. If it flows into the water body, the impact on aquatic organisms should not be underestimated. This substance may have certain toxicity and can interfere with the physiological function of aquatic organisms. If it affects the reproductive system of fish, it will reduce their reproductive ability, reduce the hatching rate of fish eggs, and increase the deformity rate of juvenile fish. In the food chain, tetrahydroxyphenyl phenol can be transmitted and accumulated along the food chain due to biological enrichment. After lower aquatic organisms ingest this substance, although the concentration is low or low, through predation, the accumulated concentration in the organisms at the top of the food chain gradually increases, which eventually affects the balance of the entire aquatic ecosystem. At the same time, if the soil is polluted by it, or the soil microbial community structure is changed, which affects the soil nutrient cycle and material transformation, it is also unfavorable to plant growth, resulting in plant dysplasia and reduced yield.
Therefore, gas methyl and tetrahydroxyphenyl phenols have a wide and far-reaching impact on the environment. It is necessary to pay attention to it, control its discharge, and prevent it from polluting the environment, so as to maintain ecological balance and human well-being.
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