Linshang Chemical
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1,2-Dichloro-4-Methoxybenzene
Linshang Chemical
|
HS Code |
940918 |
| Chemical Formula | C7H6Cl2O |
| Molar Mass | 177.028 g/mol |
| Appearance | Solid |
| Color | White to off - white |
| Odor | Typical aromatic odor |
| Melting Point | 48 - 52 °C |
| Boiling Point | 234 - 236 °C |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether, benzene |
| Vapor Pressure | Low at room temperature |
As an accredited 1,2-Dichloro-4-Methoxybenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100 - gram bottles containing 1,2 - dichloro - 4 - methoxybenzene, well - sealed for storage. |
| Storage | 1,2 - Dichloro - 4 - methoxybenzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, flames, and oxidizing agents. Store in a tightly sealed container, preferably made of corrosion - resistant materials like glass or certain plastics. Label the storage container clearly to prevent misidentification and ensure safety during handling and storage. |
| Shipping | 1,2 - dichloro - 4 - methoxybenzene is shipped in well - sealed containers, following strict chemical transportation regulations. It's transported by specialized carriers to ensure safety during transit, minimizing risks associated with this chemical. |
Competitive 1,2-Dichloro-4-Methoxybenzene 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.
We will respond to you as soon as possible.
Tel: +8615365006308
Email: info@alchemist-chem.com
Where to Buy 1,2-Dichloro-4-Methoxybenzene in China?
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Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
As a leading 1,2-Dichloro-4-Methoxybenzene 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 main uses of 1,2-dichloro-4-methoxybenzene?
1% 2C2 + - + dioxy + - + 4 + - + methoxybenzene has a wide range of main uses.
In the field of medicine, this substance can be said to be of great significance. It is often used as a key intermediate to help synthesize a variety of drugs. Taking some cardiovascular diseases as an example, 1% 2C2 + - + dioxy + - + 4 + - + methoxybenzene participates in it and plays an important role in building the active structure of the drug. Due to its special chemical structure, it can endow the drug with specific pharmacological activity and pharmacokinetic properties, helping the drug to act precisely on the human target and improve the therapeutic effect.
In the field of materials science, this substance also has a place. It can be used as a raw material for the preparation of functional materials. For example, in the synthesis of some materials with special optical or electrical properties, 1% 2C2 + - + dioxy + - + 4 + - + methoxybenzene can introduce specific functional groups through chemical reactions, thereby changing the molecular arrangement and electron cloud distribution of the material, so that the material exhibits unique optical absorption, emission or electrical conductivity properties, providing the possibility for the research and development of new optoelectronic devices, sensors and other materials.
At the same time, in the field of organic synthesis, it is an extremely important basic raw material. Organic chemists often use its chemical properties to construct more complex and diverse organic compound structures through various reactions, such as substitution reactions, addition reactions, etc., which greatly enriches the types and quantities of organic compounds, laying the foundation for the research and development of organic chemistry. In the total synthesis process of many complex natural products, 1% 2C2 + - + dioxy + - + 4 + - + methoxybenzene is involved as a starting material or key intermediate, promoting organic synthesis chemistry to a new height.
In the field of medicine, this substance can be said to be of great significance. It is often used as a key intermediate to help synthesize a variety of drugs. Taking some cardiovascular diseases as an example, 1% 2C2 + - + dioxy + - + 4 + - + methoxybenzene participates in it and plays an important role in building the active structure of the drug. Due to its special chemical structure, it can endow the drug with specific pharmacological activity and pharmacokinetic properties, helping the drug to act precisely on the human target and improve the therapeutic effect.
In the field of materials science, this substance also has a place. It can be used as a raw material for the preparation of functional materials. For example, in the synthesis of some materials with special optical or electrical properties, 1% 2C2 + - + dioxy + - + 4 + - + methoxybenzene can introduce specific functional groups through chemical reactions, thereby changing the molecular arrangement and electron cloud distribution of the material, so that the material exhibits unique optical absorption, emission or electrical conductivity properties, providing the possibility for the research and development of new optoelectronic devices, sensors and other materials.
At the same time, in the field of organic synthesis, it is an extremely important basic raw material. Organic chemists often use its chemical properties to construct more complex and diverse organic compound structures through various reactions, such as substitution reactions, addition reactions, etc., which greatly enriches the types and quantities of organic compounds, laying the foundation for the research and development of organic chemistry. In the total synthesis process of many complex natural products, 1% 2C2 + - + dioxy + - + 4 + - + methoxybenzene is involved as a starting material or key intermediate, promoting organic synthesis chemistry to a new height.
What are the physical properties of 1,2-dichloro-4-methoxybenzene?
The physical properties of 1% 2C2 + - + dioxy + - + 4 + - + methoxybenzene are as follows:
This compound is often solid or liquid, depending on the environment. Its melting temperature is an important physical property. The melting temperature is determined by the degree of solids and liquids, and the boiling temperature is the degree of liquids. However, the value depends on the accuracy.
Its density is also a physical property. The density of the compound is also determined by the amount of the material. The density can be obtained by measuring its floating and mixing properties in different media.
Solubility is also an important aspect, and its solubility varies in different solutions. In water, such as water, the solubility is limited, and the action of the water molecule is weak because the molecule contains a non-soluble group such as methoxy group. In non-soluble or weak soluble substances such as some soluble substances, the solubility is better. Due to the principle of "similar miscibility", the molecular force is more likely to make the two miscible.
In addition, on the outside, it is either transparent in color, or has a slight color, taste or specificity, but also varies due to the degree of resistance and environmental factors. Its refractive index also reflects the degree of refraction of light through the material, which can help to determine its degree and characteristics. Therefore, the general physical properties are essential for the study and application of this compound.
This compound is often solid or liquid, depending on the environment. Its melting temperature is an important physical property. The melting temperature is determined by the degree of solids and liquids, and the boiling temperature is the degree of liquids. However, the value depends on the accuracy.
Its density is also a physical property. The density of the compound is also determined by the amount of the material. The density can be obtained by measuring its floating and mixing properties in different media.
Solubility is also an important aspect, and its solubility varies in different solutions. In water, such as water, the solubility is limited, and the action of the water molecule is weak because the molecule contains a non-soluble group such as methoxy group. In non-soluble or weak soluble substances such as some soluble substances, the solubility is better. Due to the principle of "similar miscibility", the molecular force is more likely to make the two miscible.
In addition, on the outside, it is either transparent in color, or has a slight color, taste or specificity, but also varies due to the degree of resistance and environmental factors. Its refractive index also reflects the degree of refraction of light through the material, which can help to determine its degree and characteristics. Therefore, the general physical properties are essential for the study and application of this compound.
Is the chemical properties of 1,2-dichloro-4-methoxybenzene stable?
The chemical properties of 1% 2C2-dioxy-4-methoxyphenyl are quite stable. In this compound, various chemical bonds in its molecular structure interact to build a relatively stable structure. From the perspective of chemical bond energy, carbon-carbon bonds, carbon-oxygen bonds, etc. all have certain strengths, which lays the foundation for their stability.
In general chemical environments, 1% 2C2-dioxy-4-methoxyphenyl is not easy to react with common substances. For example, in the environment of water and air at room temperature and pressure, its chemical structure can maintain its original state and will not easily decompose or react with surrounding substances. This is mainly due to the electron cloud distribution of each atom in its molecule, which makes the compound have a certain resistance to external chemical substances.
Furthermore, the stability of the compound is also reflected in its tolerance to common chemical reagents. In weakly acidic or weakly basic solutions, 1% 2C2-dioxy-4-methoxyphenyl usually does not show obvious structural changes, showing good adaptability to this common chemical environment. Its stability is of great significance in many fields of chemistry. For example, in organic synthesis, it can participate in reactions as a stable structural unit, providing a stable foundation for the subsequent construction of more complex compounds. In materials science, if it is introduced into the material structure, it can improve the chemical stability of the material in a specific environment.
In general chemical environments, 1% 2C2-dioxy-4-methoxyphenyl is not easy to react with common substances. For example, in the environment of water and air at room temperature and pressure, its chemical structure can maintain its original state and will not easily decompose or react with surrounding substances. This is mainly due to the electron cloud distribution of each atom in its molecule, which makes the compound have a certain resistance to external chemical substances.
Furthermore, the stability of the compound is also reflected in its tolerance to common chemical reagents. In weakly acidic or weakly basic solutions, 1% 2C2-dioxy-4-methoxyphenyl usually does not show obvious structural changes, showing good adaptability to this common chemical environment. Its stability is of great significance in many fields of chemistry. For example, in organic synthesis, it can participate in reactions as a stable structural unit, providing a stable foundation for the subsequent construction of more complex compounds. In materials science, if it is introduced into the material structure, it can improve the chemical stability of the material in a specific environment.
What are the preparation methods of 1,2-dichloro-4-methoxybenzene?
The preparation method of 1% 2C2 + - + dioxy + - + 4 + - + methoxybenzene is as follows:
First, the phenolic compound is used as the starting material. Common phenols, such as p-cresol, can obtain the target product after specific chemical treatment. In the reactor, p-cresol is co-placed with an appropriate oxidant, such as hydrogen peroxide, and then an appropriate amount of catalyst is added, such as a compound containing iron or manganese. At a specific temperature and pressure, the methyl group of the phenols can be oxidized to gradually form the methoxybenzene structure. This process requires precise control of the reaction conditions. Excessive temperature or excessive oxidant may cause excessive oxidation of the product, affecting the yield and purity.
Second, through the aromatic electrophilic substitution reaction. Using benzene as the starting material, the methoxy group is first introduced, and the halogenated methane can be reacted with benzene in the presence of a Lewis acid catalyst, such as aluminum trichloride, to form a methyl phenyl ether. Subsequently, the methyl phenyl ether is oxidized. Oxygen or air can be used as the oxidant, and with the assistance of the catalyst, the methyl is oxidized to a dioxy structure, and then further adjusted to the target methoxybenzene. In this path, the selectivity of the electrophilic substitution reaction and the control of the conditions of the oxidation step are very critical, which are directly related to the quality and yield of the product.
Third, the halogenated benzene derivative is used as the raw material. Select a suitable halogenated benzene, such as bromobenzene, and first react with a methoxylating Then, the group at a specific position on the benzene ring is converted into dioxy and the target methoxy group structure under appropriate conditions through an oxidation reaction. This method requires attention to the activity of halobenzene, the efficiency of methoxylation reaction, and the precise regulation of subsequent oxidation steps to ensure high purity of 1% 2C2 + - + dioxy + - + 4 + - + methoxy benzene.
First, the phenolic compound is used as the starting material. Common phenols, such as p-cresol, can obtain the target product after specific chemical treatment. In the reactor, p-cresol is co-placed with an appropriate oxidant, such as hydrogen peroxide, and then an appropriate amount of catalyst is added, such as a compound containing iron or manganese. At a specific temperature and pressure, the methyl group of the phenols can be oxidized to gradually form the methoxybenzene structure. This process requires precise control of the reaction conditions. Excessive temperature or excessive oxidant may cause excessive oxidation of the product, affecting the yield and purity.
Second, through the aromatic electrophilic substitution reaction. Using benzene as the starting material, the methoxy group is first introduced, and the halogenated methane can be reacted with benzene in the presence of a Lewis acid catalyst, such as aluminum trichloride, to form a methyl phenyl ether. Subsequently, the methyl phenyl ether is oxidized. Oxygen or air can be used as the oxidant, and with the assistance of the catalyst, the methyl is oxidized to a dioxy structure, and then further adjusted to the target methoxybenzene. In this path, the selectivity of the electrophilic substitution reaction and the control of the conditions of the oxidation step are very critical, which are directly related to the quality and yield of the product.
Third, the halogenated benzene derivative is used as the raw material. Select a suitable halogenated benzene, such as bromobenzene, and first react with a methoxylating Then, the group at a specific position on the benzene ring is converted into dioxy and the target methoxy group structure under appropriate conditions through an oxidation reaction. This method requires attention to the activity of halobenzene, the efficiency of methoxylation reaction, and the precise regulation of subsequent oxidation steps to ensure high purity of 1% 2C2 + - + dioxy + - + 4 + - + methoxy benzene.
What are the precautions for storing and transporting 1,2-dichloro-4-methoxybenzene?
1% 2C2 + - + dioxy + - + 4 + - + methoxyphenyl ether must be kept in mind during storage and transportation.
The first to bear the brunt, this product has certain toxicity and irritation, so it should not be taken lightly during operation. Operators must wear professional protective clothing, protective gloves and goggles to prevent the substance from contacting the skin and eyes and causing damage to the body.
Furthermore, the storage environment is also crucial. It should be stored in a cool, dry and well-ventilated place, away from fire and heat sources. Because of its flammability, if it encounters an open flame or hot topic, it is very likely to cause serious accidents such as combustion or even explosion. At the same time, it needs to be stored separately from oxidizing agents, acids and other substances to avoid chemical reactions.
When transporting, it is also necessary to strictly follow relevant regulations. To ensure that the container is well sealed to prevent leakage. Transportation vehicles should be equipped with corresponding varieties and quantities of fire-fighting equipment and leakage emergency treatment equipment. During driving, to avoid bumps, shocks, to prevent damage to the container caused by material leakage. Once a leak occurs, emergency measures should be taken immediately, the surrounding evacuation of personnel, blockade the scene, and timely reporting to the relevant departments.
In addition, whether it is storage or transportation, the substance should be clearly marked, indicating its name, nature, hazards and other information, so that the relevant personnel can quickly identify and take the correct response measures. Only by strictly controlling these links can we ensure the safety of 1% 2C2 + - + dioxy + - + 4 + - + methoxyphenyl ether during storage and transportation.
The first to bear the brunt, this product has certain toxicity and irritation, so it should not be taken lightly during operation. Operators must wear professional protective clothing, protective gloves and goggles to prevent the substance from contacting the skin and eyes and causing damage to the body.
Furthermore, the storage environment is also crucial. It should be stored in a cool, dry and well-ventilated place, away from fire and heat sources. Because of its flammability, if it encounters an open flame or hot topic, it is very likely to cause serious accidents such as combustion or even explosion. At the same time, it needs to be stored separately from oxidizing agents, acids and other substances to avoid chemical reactions.
When transporting, it is also necessary to strictly follow relevant regulations. To ensure that the container is well sealed to prevent leakage. Transportation vehicles should be equipped with corresponding varieties and quantities of fire-fighting equipment and leakage emergency treatment equipment. During driving, to avoid bumps, shocks, to prevent damage to the container caused by material leakage. Once a leak occurs, emergency measures should be taken immediately, the surrounding evacuation of personnel, blockade the scene, and timely reporting to the relevant departments.
In addition, whether it is storage or transportation, the substance should be clearly marked, indicating its name, nature, hazards and other information, so that the relevant personnel can quickly identify and take the correct response measures. Only by strictly controlling these links can we ensure the safety of 1% 2C2 + - + dioxy + - + 4 + - + methoxyphenyl ether during storage and transportation.
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