Linshang Chemical
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1-Chloro-4-(1,1-Dimethyl Ethyl) Benzene Ether
Linshang Chemical
|
HS Code |
459052 |
| Chemical Formula | C10H13ClO |
| Molecular Weight | 184.66 |
| Appearance | Typically a liquid (description can vary based on purity and conditions) |
| Boiling Point | Data needed (varies by conditions) |
| Melting Point | Data needed (varies by conditions) |
| Density | Data needed (varies by conditions) |
| Solubility In Water | Limited solubility (non - polar nature) |
| Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether |
| Vapor Pressure | Data needed (varies by temperature) |
| Flash Point | Data needed (varies by conditions) |
| Odor | Characteristic organic odor (description can vary) |
As an accredited 1-Chloro-4-(1,1-Dimethyl Ethyl) Benzene Ether factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500 - gram bottle of 1 - chloro - 4 - (1,1 - dimethyl ethyl) benzene ether, well - sealed. |
| Storage | 1 - chloro - 4 - (1,1 - dimethylethyl) benzene ether 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 to prevent leakage and exposure to air and moisture, which could potentially cause decomposition or reactivity issues. |
| Shipping | 1 - chloro - 4 - (1,1 - dimethyl ethyl) Benzene Ether is shipped in accordance with strict chemical transportation regulations. It's typically in sealed, specialized containers to prevent leakage and ensure safe transit. |
Competitive 1-Chloro-4-(1,1-Dimethyl Ethyl) Benzene Ether prices that fit your budget—flexible terms and customized quotes for every order.
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What are the main uses of 1-chloro-4- (1,1-dimethyl Ethyl) Benzene Ether?
1 - chloro - 4 - (1,1 - dimethyl Ethyl) Benzene Ether, Chinese name 1 - chloro - 4 - (1,1 - dimethyl ethyl) phenyl ether. This substance has many uses in the work of the past.
In the field of synthesis in the past, it was often used as an important antidote. Due to the particularity of phenyl ether and the existence of chlorine atom tert-butyl, it has a specific antidote activity. For example, in some nuclei, chlorine atoms can be replaced by other nuclei, and the required functions can be introduced to create more complex compounds, which can help in the synthesis of new research and refined chemical products.
In the field of materials, it is also useful. In the synthesis process of some polymer materials, this compound can be used for modification or modification. Its benzene can increase the performance of the material, while ether can improve the flexibility of the material to a certain extent. Tert-butyl can affect the solubility and qualitative properties of the material. For example, in some high-performance engineering plastics or special materials, the rational use of this compound can improve the integrity of the material, making it more resistant to wear resistance, chemical corrosion resistance, etc.
In addition, in the early research and exploration period, this material is also often used to explore the properties of anti-corrosion. Keshijia has conducted in-depth research on various aspects of its technology, such as the shadow of anti-objects, the law of generation of objects, etc., in order to reveal the principles of transformation and reverse, and to provide the basis for the development of the whole technology, so as to promote the expansion of the field of transformation.
In the field of synthesis in the past, it was often used as an important antidote. Due to the particularity of phenyl ether and the existence of chlorine atom tert-butyl, it has a specific antidote activity. For example, in some nuclei, chlorine atoms can be replaced by other nuclei, and the required functions can be introduced to create more complex compounds, which can help in the synthesis of new research and refined chemical products.
In the field of materials, it is also useful. In the synthesis process of some polymer materials, this compound can be used for modification or modification. Its benzene can increase the performance of the material, while ether can improve the flexibility of the material to a certain extent. Tert-butyl can affect the solubility and qualitative properties of the material. For example, in some high-performance engineering plastics or special materials, the rational use of this compound can improve the integrity of the material, making it more resistant to wear resistance, chemical corrosion resistance, etc.
In addition, in the early research and exploration period, this material is also often used to explore the properties of anti-corrosion. Keshijia has conducted in-depth research on various aspects of its technology, such as the shadow of anti-objects, the law of generation of objects, etc., in order to reveal the principles of transformation and reverse, and to provide the basis for the development of the whole technology, so as to promote the expansion of the field of transformation.
What are the physical properties of 1-chloro-4- (1,1-dimethyl Ethyl) Benzene Ether
1-Chloro-4- (1,1-dimethylethyl) phenyl ether, this material has important properties and is related to many chemical applications. Its appearance is often colorless to slightly yellow transparent liquid, which is stable in ordinary environments. Looking at its odor, it has a faint aromatic taste, but it should not be ignored because of its odor or its chemical activity.
When it comes to the boiling point, it is about a certain temperature range, which is very important in the separation and purification process. The exact value of the boiling point can help craftsmen accurately control the temperature and temperature during distillation and other operations to achieve the ideal separation effect.
Furthermore, its melting point is also fixed. The level of melting point affects the physical form of this substance under different temperature conditions, which in turn affects its processing and use. In a low temperature environment, or in a solid state, and when the temperature rises, it gradually turns into a liquid state. This morphological change has far-reaching implications for its application in various formulations and processes.
Solubility is also a key physical property. 1-Chloro-4 - (1,1-dimethethyl) phenyl ether exhibits specific solubility in organic solvents. It can be soluble in some common organic solvents. This property gives it a unique advantage in the preparation of solutions, blending mixtures and other processes. By choosing a suitable solvent, its concentration and dispersion state can be adjusted to meet different production needs.
In addition, density is another important physical property. The value of its density determines its distribution in the mixing system. In liquid-liquid mixing operations, density differences can lead to phenomena such as stratification. Craftsmen can optimize the mixing process according to this characteristic to ensure uniform distribution of each ingredient and improve product quality.
This general physical property is related to each other, and together build the application basis of 1-chloro-4 - (1,1-dimethethyl) phenyl ether in the chemical industry. Whether it is synthesizing new substances or using them as additives, it is necessary to consider its physical properties in detail in order to make good use of its advantages and avoid its disadvantages.
When it comes to the boiling point, it is about a certain temperature range, which is very important in the separation and purification process. The exact value of the boiling point can help craftsmen accurately control the temperature and temperature during distillation and other operations to achieve the ideal separation effect.
Furthermore, its melting point is also fixed. The level of melting point affects the physical form of this substance under different temperature conditions, which in turn affects its processing and use. In a low temperature environment, or in a solid state, and when the temperature rises, it gradually turns into a liquid state. This morphological change has far-reaching implications for its application in various formulations and processes.
Solubility is also a key physical property. 1-Chloro-4 - (1,1-dimethethyl) phenyl ether exhibits specific solubility in organic solvents. It can be soluble in some common organic solvents. This property gives it a unique advantage in the preparation of solutions, blending mixtures and other processes. By choosing a suitable solvent, its concentration and dispersion state can be adjusted to meet different production needs.
In addition, density is another important physical property. The value of its density determines its distribution in the mixing system. In liquid-liquid mixing operations, density differences can lead to phenomena such as stratification. Craftsmen can optimize the mixing process according to this characteristic to ensure uniform distribution of each ingredient and improve product quality.
This general physical property is related to each other, and together build the application basis of 1-chloro-4 - (1,1-dimethethyl) phenyl ether in the chemical industry. Whether it is synthesizing new substances or using them as additives, it is necessary to consider its physical properties in detail in order to make good use of its advantages and avoid its disadvantages.
What are the chemical properties of 1-chloro-4- (1,1-dimethyl Ethyl) Benzene Ether?
1-Chloro-4- (1,1-dimethylethyl) phenyl ether, this is an organic compound. Looking at its structure, it contains benzene ring, chlorine atom, tert-butyl group and ether bond.
Its chemical properties are particularly interesting. Let's talk about stability first. The benzene ring has a conjugated system, which gives it certain stability. However, the presence of chlorine atoms and ether bonds makes it also reactive.
Chlorine atoms can undergo nucleophilic substitution reactions. In case of nucleophilic reagents, such as sodium alcohol, sodium phenol, etc., chlorine atoms can be replaced by nucleophilic groups to form new ether compounds. For example, when reacted with sodium ethanol, chlorine atoms will be replaced by ethoxy groups to obtain corresponding ethers. This reaction mechanism is that the nucleophilic reagent attacks the carbon atom connected to the chlorine atom, and the chlorine atom leaves with a pair of electrons to complete the substitution.
Ether bonds are generally relatively stable, but under strong acid or high temperature conditions, cracking can occur. In case of concentrated hydroiodic acid, the ether bond will break, and the corresponding iodoalkane and phenolic compounds will be formed. This is because the iodine ion in hydroiodic acid has strong nucleophilicity, attacking the carbon atoms connected to the phenyl ring in the ether bond, and the ether bond breaks.
Tert-butyl has an impact on the electron cloud density of the phenyl ring due to the large steric barrier. It makes the electron cloud density of the phenyl ring ortho and para-site relatively high, and the electrophilic substitution reaction is more likely to For example, when nitrification occurs, the nitro group tends to enter the adjacent and para-site of the tert-butyl group.
Furthermore, this compound can undergo oxidation reactions. In case of strong oxidants, such as potassium permanganate, the tert-butyl group of the side chain of the benzene ring may be oxidized, but due to the special structure of the tert-butyl group, the oxidation product is more complicated.
In summary, 1-chloro-4 - (1,1-dimethethyl) phenyl ether has rich chemical properties and can undergo a variety of reactions. These reaction characteristics provide many possibilities for the field of organic synthesis, and many valuable organic compounds can be synthesized through clever design of reaction routes.
Its chemical properties are particularly interesting. Let's talk about stability first. The benzene ring has a conjugated system, which gives it certain stability. However, the presence of chlorine atoms and ether bonds makes it also reactive.
Chlorine atoms can undergo nucleophilic substitution reactions. In case of nucleophilic reagents, such as sodium alcohol, sodium phenol, etc., chlorine atoms can be replaced by nucleophilic groups to form new ether compounds. For example, when reacted with sodium ethanol, chlorine atoms will be replaced by ethoxy groups to obtain corresponding ethers. This reaction mechanism is that the nucleophilic reagent attacks the carbon atom connected to the chlorine atom, and the chlorine atom leaves with a pair of electrons to complete the substitution.
Ether bonds are generally relatively stable, but under strong acid or high temperature conditions, cracking can occur. In case of concentrated hydroiodic acid, the ether bond will break, and the corresponding iodoalkane and phenolic compounds will be formed. This is because the iodine ion in hydroiodic acid has strong nucleophilicity, attacking the carbon atoms connected to the phenyl ring in the ether bond, and the ether bond breaks.
Tert-butyl has an impact on the electron cloud density of the phenyl ring due to the large steric barrier. It makes the electron cloud density of the phenyl ring ortho and para-site relatively high, and the electrophilic substitution reaction is more likely to For example, when nitrification occurs, the nitro group tends to enter the adjacent and para-site of the tert-butyl group.
Furthermore, this compound can undergo oxidation reactions. In case of strong oxidants, such as potassium permanganate, the tert-butyl group of the side chain of the benzene ring may be oxidized, but due to the special structure of the tert-butyl group, the oxidation product is more complicated.
In summary, 1-chloro-4 - (1,1-dimethethyl) phenyl ether has rich chemical properties and can undergo a variety of reactions. These reaction characteristics provide many possibilities for the field of organic synthesis, and many valuable organic compounds can be synthesized through clever design of reaction routes.
What is the production method of 1-chloro-4- (1,1-dimethyl Ethyl) Benzene Ether?
1-Chloro-4- (1,1-dimethethyl) phenyl ether. The preparation method of this substance is not explicitly stated in the book "Tiangong Kaiwu", but it can be deduced according to the principle of similar chemistry.
In the past chemical preparation, to obtain such phenyl ether compounds containing specific substituents often involves nucleophilic substitution. First, it is necessary to prepare a suitable halogenated benzene derivative, that is, 1-chloro-4- (1,1-dimethethyl) benzene. This halogenated benzene can be obtained by halogenation of the corresponding benzene derivative. For example, with p (1,1-dimethylethyl) benzene as the starting material, under suitable halogenation conditions, such as in the presence of light or catalyst, the reaction with chlorine can introduce chlorine atoms to obtain 1-chloro-4- (1,1-dimethylethyl) benzene.
Then, to convert it into an ether, it is often nucleophilic substitution with alkoxides or phenolates. Appropriate alcohols or phenols can be selected to react with bases to form corresponding alkoxides or phenolates. If a suitable alcohol, such as an alkyl alcohol, interacts with a base such as sodium metal or sodium hydroxide to form sodium alcohol. After that, the sodium alcohol is mixed with 1-chloro-4- (1,1-dimethylethyl) benzene, and in a suitable temperature and solvent environment, the oxygen anion of the sodium alcohol acts as a nucleophilic reagent to attack the carbon atom connected to the chlorine atom of the halogenated benzene, and the chlorine atom leaves to form an ether bond, resulting in 1-chloro-4- (1,1-dimethethyl) phenyl ether.
Or, if phenols are used as raw materials, the phenol is first reacted with a base to form a phenol salt, and then with the halogenated benzene according to the above-mentioned similar nucleophilic substitution steps, under suitable reaction conditions, the target compound can also be prepared. In the reaction process, the choice of solvent is very critical. Commonly used polar aprotic solvents, such as N, N-dimethylformamide (DMF) or dimethyl sulfoxide (DMSO), can promote the activity of nucleophiles, improve the reaction rate and yield. The control of temperature cannot be ignored. The reaction temperature needs to be carefully adjusted according to the activity of the reactants and the difficulty of the reaction to achieve the best reaction effect.
In the past chemical preparation, to obtain such phenyl ether compounds containing specific substituents often involves nucleophilic substitution. First, it is necessary to prepare a suitable halogenated benzene derivative, that is, 1-chloro-4- (1,1-dimethethyl) benzene. This halogenated benzene can be obtained by halogenation of the corresponding benzene derivative. For example, with p (1,1-dimethylethyl) benzene as the starting material, under suitable halogenation conditions, such as in the presence of light or catalyst, the reaction with chlorine can introduce chlorine atoms to obtain 1-chloro-4- (1,1-dimethylethyl) benzene.
Then, to convert it into an ether, it is often nucleophilic substitution with alkoxides or phenolates. Appropriate alcohols or phenols can be selected to react with bases to form corresponding alkoxides or phenolates. If a suitable alcohol, such as an alkyl alcohol, interacts with a base such as sodium metal or sodium hydroxide to form sodium alcohol. After that, the sodium alcohol is mixed with 1-chloro-4- (1,1-dimethylethyl) benzene, and in a suitable temperature and solvent environment, the oxygen anion of the sodium alcohol acts as a nucleophilic reagent to attack the carbon atom connected to the chlorine atom of the halogenated benzene, and the chlorine atom leaves to form an ether bond, resulting in 1-chloro-4- (1,1-dimethethyl) phenyl ether.
Or, if phenols are used as raw materials, the phenol is first reacted with a base to form a phenol salt, and then with the halogenated benzene according to the above-mentioned similar nucleophilic substitution steps, under suitable reaction conditions, the target compound can also be prepared. In the reaction process, the choice of solvent is very critical. Commonly used polar aprotic solvents, such as N, N-dimethylformamide (DMF) or dimethyl sulfoxide (DMSO), can promote the activity of nucleophiles, improve the reaction rate and yield. The control of temperature cannot be ignored. The reaction temperature needs to be carefully adjusted according to the activity of the reactants and the difficulty of the reaction to achieve the best reaction effect.
What are the precautions for storing and transporting 1-chloro-4- (1,1-dimethyl Ethyl) Benzene Ether?
1-Chloro-4- (1,1-dimethylethyl) phenyl ether, this is an organic compound. When storing and transporting, many key matters must be paid attention to.
One is related to storage. Because it may have a certain chemical activity, it needs to find a cool, dry and well-ventilated place to store it. If placed in a high temperature and humid place, it may cause chemical reactions and cause it to deteriorate. For example, under high temperature, the chemical bonds inside the compound may be more active, and it is easy to react with certain components in the air, which will damage its purity and quality.
Second, for transportation, it must be operated in accordance with relevant regulations and standards. The transportation container must be strong and well sealed to prevent leakage. If this compound leaks, or pollutes the environment, or even endangers the surrounding organisms. During handling, it should also be handled with care to avoid damage to the container due to collision and vibration.
In addition, whether it is stored or transported, it is necessary to have a detailed understanding of the characteristics of the compound. Know its chemical properties, such as stability and solubility, so that appropriate measures can be taken quickly in case of a situation. In case of leakage, according to its solubility, suitable materials can be selected for adsorption and cleaning.
In addition, obvious warning signs should be set up at storage and transportation sites to remind personnel to pay attention. The relevant operators must also be professionally trained and familiar with the operation process and emergency response methods, so as to ensure the safety of 1-chloro-4- (1,1-dimethethyl) phenyl ether during storage and transportation.
One is related to storage. Because it may have a certain chemical activity, it needs to find a cool, dry and well-ventilated place to store it. If placed in a high temperature and humid place, it may cause chemical reactions and cause it to deteriorate. For example, under high temperature, the chemical bonds inside the compound may be more active, and it is easy to react with certain components in the air, which will damage its purity and quality.
Second, for transportation, it must be operated in accordance with relevant regulations and standards. The transportation container must be strong and well sealed to prevent leakage. If this compound leaks, or pollutes the environment, or even endangers the surrounding organisms. During handling, it should also be handled with care to avoid damage to the container due to collision and vibration.
In addition, whether it is stored or transported, it is necessary to have a detailed understanding of the characteristics of the compound. Know its chemical properties, such as stability and solubility, so that appropriate measures can be taken quickly in case of a situation. In case of leakage, according to its solubility, suitable materials can be selected for adsorption and cleaning.
In addition, obvious warning signs should be set up at storage and transportation sites to remind personnel to pay attention. The relevant operators must also be professionally trained and familiar with the operation process and emergency response methods, so as to ensure the safety of 1-chloro-4- (1,1-dimethethyl) phenyl ether during storage and transportation.
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