Linshang Chemical
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1,2-Dichloro-3-(Chloromethyl)Benzene
Linshang Chemical
|
HS Code |
776680 |
| Chemical Formula | C7H5Cl3 |
| Molar Mass | 195.47 g/mol |
| Appearance | Colorless to light yellow liquid |
| Boiling Point | Around 220 - 230 °C |
| Density | Approx. 1.38 - 1.42 g/cm³ |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in common organic solvents like benzene, toluene |
| Vapor Pressure | Low vapor pressure at room temperature |
| Odor | Pungent, characteristic chlorinated aromatic odor |
As an accredited 1,2-Dichloro-3-(Chloromethyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 1,2 - dichloro - 3-(chloromethyl)benzene in a sealed glass bottle. |
| Storage | 1,2 - Dichloro - 3 - (chloromethyl)benzene should be stored in a cool, well - ventilated area, away from heat and ignition sources. Keep it in a tightly sealed container, preferably made of corrosion - resistant materials. Store it separately from oxidizing agents, acids, and bases. Ensure storage facilities are in compliance with safety regulations to prevent leakage and potential hazards. |
| Shipping | 1,2 - Dichloro - 3 - (chloromethyl)benzene is a chemical that must be shipped in accordance with strict hazardous materials regulations. It should be in properly sealed, corrosion - resistant containers, labeled clearly, and transported by carriers licensed for such chemicals. |
Competitive 1,2-Dichloro-3-(Chloromethyl)Benzene 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-3-(Chloromethyl)Benzene in China?
As a trusted 1,2-Dichloro-3-(Chloromethyl)Benzene manufacturer, we deliver:
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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-3-(Chloromethyl)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 physical properties of 1,2-dichloro-3- (chloromethyl) benzene?
1% 2C2 -dioxo-3- (oxomethyl) indole, the properties of this substance are as follows:
It is an organic compound, the appearance is often crystalline solid, the color is or colorless, or with a slight yellowish, fine texture.
The melting point is in a specific range. At this temperature, the substance changes from solid to liquid state, which is of great significance for its purification, identification and control under specific reaction conditions.
The boiling point is also in the corresponding range, and the gas-liquid equilibrium during boiling has a profound impact on its separation, purification and reaction system construction.
In terms of solubility, it has a certain solubility in some organic solvents such as ethanol and ether, and its solubility in water is poor. This property needs to be taken into account in its extraction, separation and reaction solvent selection.
In terms of stability, it can exist stably at room temperature and pressure, and can be changed by chemical reaction under specific conditions such as high temperature and strong oxidizing agent. When storing and using, such conditions should be avoided to ensure the stability of its chemical structure and properties.
The physical properties of 1% 2C2-dioxy-3- (oxomethyl) indole are widely used in chemical industry, medicine and other fields. It plays a key role in synthesis reactions, dosage form preparation, etc. Only by understanding its physical properties can it better exert its effectiveness.
It is an organic compound, the appearance is often crystalline solid, the color is or colorless, or with a slight yellowish, fine texture.
The melting point is in a specific range. At this temperature, the substance changes from solid to liquid state, which is of great significance for its purification, identification and control under specific reaction conditions.
The boiling point is also in the corresponding range, and the gas-liquid equilibrium during boiling has a profound impact on its separation, purification and reaction system construction.
In terms of solubility, it has a certain solubility in some organic solvents such as ethanol and ether, and its solubility in water is poor. This property needs to be taken into account in its extraction, separation and reaction solvent selection.
In terms of stability, it can exist stably at room temperature and pressure, and can be changed by chemical reaction under specific conditions such as high temperature and strong oxidizing agent. When storing and using, such conditions should be avoided to ensure the stability of its chemical structure and properties.
The physical properties of 1% 2C2-dioxy-3- (oxomethyl) indole are widely used in chemical industry, medicine and other fields. It plays a key role in synthesis reactions, dosage form preparation, etc. Only by understanding its physical properties can it better exert its effectiveness.
What are the chemical properties of 1,2-dichloro-3- (chloromethyl) benzene?
1% 2C2-carbon dioxide-3- (methoxy) benzene is one of the organic compounds. Its chemical properties are quite interesting, let me explain in detail for you.
First of all, its reaction with acids and bases. In this compound, the electron cloud distribution of the benzene ring is affected by methoxy and carbon dioxide-related groups. Methoxy groups have the effect of electron conductors, which can increase the density of electron clouds in the adjacent and para-sites of the benzene ring. When encountering electrophilic reagents, the reaction easily occurs in the adjacent and para-sites. However, if the carbon dioxide-related groups are properly converted, they can participate in the reaction under alkaline conditions. In the case of strong bases, some of the carbon dioxide may react with the bases to neutralize and form corresponding salts.
times and redox properties. The benzene ring of this compound is relatively stable, but under the action of specific strong oxidants, the benzene ring may be destroyed or side chain oxidation occurs. If there is a suitable reducing agent, the carbon attached to the methoxy group may be reduced, but these reactions require precise control of the reaction conditions.
Furthermore, the substitution reaction is quite important. Due to the localization effect of methoxy groups, electrophilic substitution reactions such as halogenation and nitrification mostly occur in the adjacent and para-sites of the benzene ring. For example, the halogenation reaction on the benzene ring can be realized with halogen elements in the presence of appropriate catalysts, and the products are mainly adjacent and para-isomers.
In addition, the spatial structure of this compound also affects its properties. The spatial arrangement of methoxy groups and carbon dioxide-related parts may affect the interaction between molecules, which in turn affects its physical properties, such as melting point, boiling point, etc. The differences in these physical properties will indirectly affect its reactivity and selectivity in different reaction systems.
In short, the chemical properties of 1% 2C2-carbon dioxide-3- (methoxy) benzene are rich and diverse, and may have important application value in organic synthesis and other fields. However, in order to make full use of its properties, it is necessary to further explore the precise regulation of various reaction conditions.
First of all, its reaction with acids and bases. In this compound, the electron cloud distribution of the benzene ring is affected by methoxy and carbon dioxide-related groups. Methoxy groups have the effect of electron conductors, which can increase the density of electron clouds in the adjacent and para-sites of the benzene ring. When encountering electrophilic reagents, the reaction easily occurs in the adjacent and para-sites. However, if the carbon dioxide-related groups are properly converted, they can participate in the reaction under alkaline conditions. In the case of strong bases, some of the carbon dioxide may react with the bases to neutralize and form corresponding salts.
times and redox properties. The benzene ring of this compound is relatively stable, but under the action of specific strong oxidants, the benzene ring may be destroyed or side chain oxidation occurs. If there is a suitable reducing agent, the carbon attached to the methoxy group may be reduced, but these reactions require precise control of the reaction conditions.
Furthermore, the substitution reaction is quite important. Due to the localization effect of methoxy groups, electrophilic substitution reactions such as halogenation and nitrification mostly occur in the adjacent and para-sites of the benzene ring. For example, the halogenation reaction on the benzene ring can be realized with halogen elements in the presence of appropriate catalysts, and the products are mainly adjacent and para-isomers.
In addition, the spatial structure of this compound also affects its properties. The spatial arrangement of methoxy groups and carbon dioxide-related parts may affect the interaction between molecules, which in turn affects its physical properties, such as melting point, boiling point, etc. The differences in these physical properties will indirectly affect its reactivity and selectivity in different reaction systems.
In short, the chemical properties of 1% 2C2-carbon dioxide-3- (methoxy) benzene are rich and diverse, and may have important application value in organic synthesis and other fields. However, in order to make full use of its properties, it is necessary to further explore the precise regulation of various reaction conditions.
What are the main uses of 1,2-dichloro-3- (chloromethyl) benzene?
1% 2C2 + - + dioxy + - + 3- (oxomethyl) naphthalene, the 1,2-dioxy-3- (oxomethyl) naphthalene involved in this name, has important uses in many fields.
In the field of pharmaceutical research and development, 1,2-dioxy-3- (oxomethyl) naphthalene may provide key raw materials for the creation of new drugs. Its unique chemical structure may interact with specific biological targets, laying the foundation for the development of drugs for the treatment of specific diseases. For example, through clever chemical modification and modification, compounds with unique pharmacological activities may be obtained to overcome difficult diseases such as inflammation and tumors.
In the field of materials science, 1,2-dioxy-3- (oxomethyl) naphthalene can participate in the preparation of high-performance materials. Due to its specific physical and chemical properties, it can be added to a specific material system to improve the properties of materials, such as enhancing the stability of materials and improving their electrical properties, and then preparing high-performance materials suitable for electronic devices, optical materials and other fields.
In organic synthesis chemistry, 1,2-dioxy-3- (oxomethyl) naphthalene plays an indispensable role as a key intermediate. Organic chemists can realize the construction of complex organic compounds by performing various chemical reactions on it. Through ingenious reaction design, using 1,2-dioxy-3- (oxomethyl) naphthalene as the starting material, organic molecules with specific structures and functions can be gradually built, enriching the variety and structural diversity of organic compounds, and injecting new impetus into the development of organic synthetic chemistry.
In the field of pharmaceutical research and development, 1,2-dioxy-3- (oxomethyl) naphthalene may provide key raw materials for the creation of new drugs. Its unique chemical structure may interact with specific biological targets, laying the foundation for the development of drugs for the treatment of specific diseases. For example, through clever chemical modification and modification, compounds with unique pharmacological activities may be obtained to overcome difficult diseases such as inflammation and tumors.
In the field of materials science, 1,2-dioxy-3- (oxomethyl) naphthalene can participate in the preparation of high-performance materials. Due to its specific physical and chemical properties, it can be added to a specific material system to improve the properties of materials, such as enhancing the stability of materials and improving their electrical properties, and then preparing high-performance materials suitable for electronic devices, optical materials and other fields.
In organic synthesis chemistry, 1,2-dioxy-3- (oxomethyl) naphthalene plays an indispensable role as a key intermediate. Organic chemists can realize the construction of complex organic compounds by performing various chemical reactions on it. Through ingenious reaction design, using 1,2-dioxy-3- (oxomethyl) naphthalene as the starting material, organic molecules with specific structures and functions can be gradually built, enriching the variety and structural diversity of organic compounds, and injecting new impetus into the development of organic synthetic chemistry.
What is the preparation method of 1,2-dichloro-3- (chloromethyl) benzene?
To prepare 1% 2C2-dioxy-3- (oxomethyl) indole, the method is as follows:
First take an appropriate amount of starting material, which needs to be carefully selected and pretreated to ensure its purity and quality, in order to lay a good foundation for the subsequent reaction.
Then, in a suitable reaction vessel, add the selected raw material in a specific ratio, and add an appropriate amount of catalyst. The amount and type of catalyst are crucial, which has a great impact on the reaction rate and product purity, and need to be precisely controlled.
Next, adjust the reaction temperature and pressure to the set value. The precise control of temperature and pressure is the key. Different stages of the reaction have different requirements. They may need to be gradually heated up, lowered in pressure, or maintained at constant temperature and pressure, all of which need to be flexibly adjusted according to the reaction process.
During the reaction process, it is necessary to closely observe the reaction phenomena, such as color changes, gas escape, etc., in order to determine the progress of the reaction and whether there is any abnormality.
After the reaction is roughly completed, a series of post-processing steps are required. First, extract with a suitable solvent, and separate the product from the reaction system to remove impurities. The product is further purified by distillation, recrystallization, etc., to achieve the required purity standard.
The whole preparation process requires the experimenter to have exquisite skills, rigorous attitude, and careful operation of each step to successfully prepare 1% 2C2-dioxy-3- (oxomethyl) indole.
First take an appropriate amount of starting material, which needs to be carefully selected and pretreated to ensure its purity and quality, in order to lay a good foundation for the subsequent reaction.
Then, in a suitable reaction vessel, add the selected raw material in a specific ratio, and add an appropriate amount of catalyst. The amount and type of catalyst are crucial, which has a great impact on the reaction rate and product purity, and need to be precisely controlled.
Next, adjust the reaction temperature and pressure to the set value. The precise control of temperature and pressure is the key. Different stages of the reaction have different requirements. They may need to be gradually heated up, lowered in pressure, or maintained at constant temperature and pressure, all of which need to be flexibly adjusted according to the reaction process.
During the reaction process, it is necessary to closely observe the reaction phenomena, such as color changes, gas escape, etc., in order to determine the progress of the reaction and whether there is any abnormality.
After the reaction is roughly completed, a series of post-processing steps are required. First, extract with a suitable solvent, and separate the product from the reaction system to remove impurities. The product is further purified by distillation, recrystallization, etc., to achieve the required purity standard.
The whole preparation process requires the experimenter to have exquisite skills, rigorous attitude, and careful operation of each step to successfully prepare 1% 2C2-dioxy-3- (oxomethyl) indole.
What are the precautions for the use of 1,2-dichloro-3- (chloromethyl) benzene?
1% 2C2 -dioxide- 3- (methoxy) benzene should pay attention to the following things during use:
First, it is related to storage. This substance must be stored in a cool, dry and well-ventilated place. Because of its certain chemical activity, if the storage environment is not good, such as high temperature and humidity, it is very likely to cause deterioration, which will affect its quality and performance. Do not mix with oxidants, acids and other substances to prevent dangerous chemical reactions and endanger safety.
Second, when using the operation. Operators should strictly follow the standard procedures and wear appropriate protective equipment, such as protective gloves, goggles, etc. This substance may be irritating to the skin and eyes. If it is inadvertently exposed, it should be rinsed with a large amount of water immediately and seek medical attention in time according to the actual situation. In the process of taking it, the action should be stable and accurate to avoid spilling and waste.
Third, it involves a chemical reaction. In view of its structural characteristics, when participating in a chemical reaction, the reaction conditions need to be strictly controlled. Temperature, pH and other factors have a significant impact on the reaction process and product formation. If the reaction temperature is too high, or side reactions increase, reducing the purity of the product; if the pH is not suitable, the reaction may not proceed smoothly. Therefore, the reaction conditions should be carefully explored and precisely regulated before the reaction.
Fourth, waste disposal. Waste after use cannot be discarded at will. Proper disposal should be carried out in accordance with relevant environmental protection regulations. Because it may contain ingredients harmful to the environment, if not disposed of properly, it will cause pollution to soil, water sources, etc. Specific procedures must be followed for harmless treatment to ensure environmental safety.
First, it is related to storage. This substance must be stored in a cool, dry and well-ventilated place. Because of its certain chemical activity, if the storage environment is not good, such as high temperature and humidity, it is very likely to cause deterioration, which will affect its quality and performance. Do not mix with oxidants, acids and other substances to prevent dangerous chemical reactions and endanger safety.
Second, when using the operation. Operators should strictly follow the standard procedures and wear appropriate protective equipment, such as protective gloves, goggles, etc. This substance may be irritating to the skin and eyes. If it is inadvertently exposed, it should be rinsed with a large amount of water immediately and seek medical attention in time according to the actual situation. In the process of taking it, the action should be stable and accurate to avoid spilling and waste.
Third, it involves a chemical reaction. In view of its structural characteristics, when participating in a chemical reaction, the reaction conditions need to be strictly controlled. Temperature, pH and other factors have a significant impact on the reaction process and product formation. If the reaction temperature is too high, or side reactions increase, reducing the purity of the product; if the pH is not suitable, the reaction may not proceed smoothly. Therefore, the reaction conditions should be carefully explored and precisely regulated before the reaction.
Fourth, waste disposal. Waste after use cannot be discarded at will. Proper disposal should be carried out in accordance with relevant environmental protection regulations. Because it may contain ingredients harmful to the environment, if not disposed of properly, it will cause pollution to soil, water sources, etc. Specific procedures must be followed for harmless treatment to ensure environmental safety.
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