Linshang Chemical
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1,3-Dichloro-2-(Chloromethyl)Benzene
Linshang Chemical
|
HS Code |
602425 |
| Chemical Formula | C7H5Cl3 |
| Molar Mass | 195.47 g/mol |
| Appearance | Colorless to light yellow liquid |
| Boiling Point | Approximately 240 - 245 °C |
| Density | Around 1.38 - 1.42 g/cm³ |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in many organic solvents like ethanol, ether |
| Odor | Pungent, characteristic aromatic odor |
As an accredited 1,3-Dichloro-2-(Chloromethyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500 - gram bottle packaging for 1,3 - dichloro - 2 - (chloromethyl)benzene. |
| Storage | 1,3 - Dichloro - 2-(chloromethyl)benzene should be stored in a cool, well - ventilated area away from heat and ignition sources. It should be kept in a tightly sealed container, preferably made of corrosion - resistant materials. Store it separately from oxidizing agents, bases, and other reactive chemicals to prevent potential reactions. Ensure proper labeling for easy identification. |
| Shipping | 1,3 - dichloro - 2 - (chloromethyl)benzene is a chemical. Shipping should be in accordance with hazardous material regulations. It must be properly packaged to prevent leakage and transported by approved carriers with safety precautions. |
Competitive 1,3-Dichloro-2-(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.
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Tel: +8615365006308
Email: info@alchemist-chem.com
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As a leading 1,3-Dichloro-2-(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 main uses of 1,3-dichloro-2- (chloromethyl) benzene?
1% 2C3 -dideuterium-2- (deuteromethyl) benzene, an intermediary for organic synthesis. In the field of organic chemistry, it plays an important role and is mostly used in the preparation of specific organic compounds.
With it as a starting material, chemists can use various chemical reactions, such as substitution reactions, addition reactions, etc., to construct organic molecules with more complex structures and unique functions. For example, in pharmaceutical chemistry, it can be converted into drug molecules with specific pharmacological activities through ingenious reaction paths, providing a key foundation for the development of new drugs.
In the field of materials science, with the help of the reaction of this compound, new materials with special electrical, optical and mechanical properties may be prepared to meet the needs of high-tech industries for special materials.
In the strategic design of organic synthesis, 1% 2C3 -dideuterium-2 - (deuterium methyl) benzene, because of its specific deuterium atom and methyl structure, endows the reaction product with unique isotope labels and structural characteristics, which is convenient for scientists to track the reaction process and explore the reaction mechanism. It is of great significance for in-depth understanding of the essence of organic chemical reactions, and then optimizing reaction conditions, improving reaction efficiency and selectivity.
With it as a starting material, chemists can use various chemical reactions, such as substitution reactions, addition reactions, etc., to construct organic molecules with more complex structures and unique functions. For example, in pharmaceutical chemistry, it can be converted into drug molecules with specific pharmacological activities through ingenious reaction paths, providing a key foundation for the development of new drugs.
In the field of materials science, with the help of the reaction of this compound, new materials with special electrical, optical and mechanical properties may be prepared to meet the needs of high-tech industries for special materials.
In the strategic design of organic synthesis, 1% 2C3 -dideuterium-2 - (deuterium methyl) benzene, because of its specific deuterium atom and methyl structure, endows the reaction product with unique isotope labels and structural characteristics, which is convenient for scientists to track the reaction process and explore the reaction mechanism. It is of great significance for in-depth understanding of the essence of organic chemical reactions, and then optimizing reaction conditions, improving reaction efficiency and selectivity.
What are the physical properties of 1,3-dichloro-2- (chloromethyl) benzene?
1% 2C3-dioxy-2- (oxomethyl) benzene, is a kind of organic compound. Its physical properties are as follows:
Looking at its appearance, under room temperature and pressure, it is mostly colorless to light yellow liquid, with a clear texture. Under the sun, there may be a shimmering light, just like the beginning of jade dew condensation, and it is full of agility in circulation.
The smell of smell often has a special aroma, but it is not a rich and intolerable fragrance. It is a quiet and slightly spicy smell, similar to the light fragrance scattered by quaint sachets. Although it is not strong, it can linger on the nose and attract reverie.
When it comes to melting and boiling point, its melting point is low, just like when spring snow is warm, it turns into a liquid phase when it warms up; the boiling point varies according to the specific environmental pressure, and is roughly between a certain temperature range. If the temperature is properly controlled, it can be vaporized and risen at a specific temperature, just like clouds and mist.
As for solubility, this substance has good solubility in organic solvents, such as fish get water, and can dissolve with organic solvents such as ethanol and ether, and fuse into one, regardless of each other; however, its solubility in water is not good, just like oil and water are difficult to blend, and the two meet and are distinct.
In terms of density, compared to water, its density may be different, or lighter than water, floating on the water surface, such as thin feathers floating; or heavier than water, sinking at the bottom of the water, like jade hidden deep.
In addition, the volatility of this substance is also a characteristic. Under appropriate conditions, it can evaporate slowly, just like the fragrance of flowers overflowing, gradually diffusing in the surrounding space, leaving a trace of smell. Its vapor pressure also has a specific value, which is closely related to temperature. When the temperature increases, the vapor pressure increases, just like hot steam evaporation, which is more likely to escape into the air.
Looking at its appearance, under room temperature and pressure, it is mostly colorless to light yellow liquid, with a clear texture. Under the sun, there may be a shimmering light, just like the beginning of jade dew condensation, and it is full of agility in circulation.
The smell of smell often has a special aroma, but it is not a rich and intolerable fragrance. It is a quiet and slightly spicy smell, similar to the light fragrance scattered by quaint sachets. Although it is not strong, it can linger on the nose and attract reverie.
When it comes to melting and boiling point, its melting point is low, just like when spring snow is warm, it turns into a liquid phase when it warms up; the boiling point varies according to the specific environmental pressure, and is roughly between a certain temperature range. If the temperature is properly controlled, it can be vaporized and risen at a specific temperature, just like clouds and mist.
As for solubility, this substance has good solubility in organic solvents, such as fish get water, and can dissolve with organic solvents such as ethanol and ether, and fuse into one, regardless of each other; however, its solubility in water is not good, just like oil and water are difficult to blend, and the two meet and are distinct.
In terms of density, compared to water, its density may be different, or lighter than water, floating on the water surface, such as thin feathers floating; or heavier than water, sinking at the bottom of the water, like jade hidden deep.
In addition, the volatility of this substance is also a characteristic. Under appropriate conditions, it can evaporate slowly, just like the fragrance of flowers overflowing, gradually diffusing in the surrounding space, leaving a trace of smell. Its vapor pressure also has a specific value, which is closely related to temperature. When the temperature increases, the vapor pressure increases, just like hot steam evaporation, which is more likely to escape into the air.
What are the chemical properties of 1,3-dichloro-2- (chloromethyl) benzene?
1% 2C3 -dideuterium-2- (deuterium methyl) benzene is an organic compound with unique chemical properties. Let me explain in detail for you.
In this compound, the introduction of deuterium atoms affects its physical and chemical properties. Deuterium is more massive than hydrogen, and this difference makes the C-D bond stronger than the C-H bond. In many chemical reactions, the reaction rate of the step involving C-D bond breaking is often lower than that of those involving C-H bond breaking, which is the kinetic isotope effect.
In the substitution reaction, 1% 2C3 -dideuterium-2- (deuterium methyl) benzene exhibits certain characteristics. Due to the substituent layout on the benzene ring, the localization effect of the substituent is significant during the electrophilic substitution reaction. The methyl group on the benzene ring is an ortho-and para-locator, but due to the presence of deuterium atoms, the electron cloud distribution changes slightly, which in turn affects the attack position and reactivity of the electrophilic reagents.
In terms of oxidation reaction, it is similar to ordinary methyl-containing benzene, and the methyl group of this compound can be oxidized. However, due to the influence of deuterium, the oxidation reaction process may be slightly different from that of ordinary ben For example, in the process of methyl oxidation to carboxyl groups under the action of specific oxidants, the C-D bond breaking step may be slower, resulting in changes in the overall oxidation rate.
In addition, in high temperature cracking or other reactions involving chemical bond breaking, the difference in the stability of the C-D bond and the C-C bond in 1% 2C3 -dideuterium-2 - (deuterium methyl) benzene also affects the reaction path and product distribution.
Overall, the introduction of 1% 2C3 -dideuterium-2- (deuterium-methyl) benzene deuterium atoms not only has similarities with ordinary benzene derivatives, but also has unique characteristics due to isotopic effects. It is an important research object in the study of reactions and mechanisms in organic chemistry.
In this compound, the introduction of deuterium atoms affects its physical and chemical properties. Deuterium is more massive than hydrogen, and this difference makes the C-D bond stronger than the C-H bond. In many chemical reactions, the reaction rate of the step involving C-D bond breaking is often lower than that of those involving C-H bond breaking, which is the kinetic isotope effect.
In the substitution reaction, 1% 2C3 -dideuterium-2- (deuterium methyl) benzene exhibits certain characteristics. Due to the substituent layout on the benzene ring, the localization effect of the substituent is significant during the electrophilic substitution reaction. The methyl group on the benzene ring is an ortho-and para-locator, but due to the presence of deuterium atoms, the electron cloud distribution changes slightly, which in turn affects the attack position and reactivity of the electrophilic reagents.
In terms of oxidation reaction, it is similar to ordinary methyl-containing benzene, and the methyl group of this compound can be oxidized. However, due to the influence of deuterium, the oxidation reaction process may be slightly different from that of ordinary ben For example, in the process of methyl oxidation to carboxyl groups under the action of specific oxidants, the C-D bond breaking step may be slower, resulting in changes in the overall oxidation rate.
In addition, in high temperature cracking or other reactions involving chemical bond breaking, the difference in the stability of the C-D bond and the C-C bond in 1% 2C3 -dideuterium-2 - (deuterium methyl) benzene also affects the reaction path and product distribution.
Overall, the introduction of 1% 2C3 -dideuterium-2- (deuterium-methyl) benzene deuterium atoms not only has similarities with ordinary benzene derivatives, but also has unique characteristics due to isotopic effects. It is an important research object in the study of reactions and mechanisms in organic chemistry.
What is the production method of 1,3-dichloro-2- (chloromethyl) benzene?
The preparation method of 1% 2C3-dihydro-2- (hydromethyl) naphthalene can be carried out according to the following method.
First take an appropriate amount of naphthalene derivatives as the starting material. This material should have a specific substituent to facilitate the subsequent reaction. The starting material is placed in a suitable reaction vessel, which must be able to withstand a certain temperature and pressure, and has good sealing.
Subsequently, an appropriate amount of catalyst is added to the reaction vessel. When this catalyst has high activity and selectivity, it can promote the reaction in the direction of generating the target product. Commonly used catalysts or metal complexes can effectively reduce the activation energy of the reaction and accelerate the reaction rate.
Then inject a suitable hydrogen source into it for the addition reaction of dihydrogen. The hydrogen source can be selected from common substances such as hydrogen. Before entering the reaction system, its purity must be ensured to prevent impurities from affecting the reaction process.
React under suitable temperature and pressure conditions. The regulation of temperature and pressure is extremely critical. Improper temperature and pressure conditions may cause the reaction rate to be too slow, or cause side reactions. Generally speaking, the temperature can be maintained in a specific range, such as between [X] ° C and [X] ° C, and the pressure is also controlled in the range of [X] MPa to [X] MPa. Under these conditions, the starting material reacts with a hydrogen source under the action of a catalyst to gradually generate 1% 2C3-dihydro-2- (hydromethyl) naphthalene.
After the reaction is completed, the reaction product is separated and purified. Common separation methods such as distillation, extraction, column chromatography, etc. can be used to obtain high-purity target products. After fine separation and purification operations, the desired 1% 2C3-dihydro-2- (hydromethyl) naphthalene can be obtained.
First take an appropriate amount of naphthalene derivatives as the starting material. This material should have a specific substituent to facilitate the subsequent reaction. The starting material is placed in a suitable reaction vessel, which must be able to withstand a certain temperature and pressure, and has good sealing.
Subsequently, an appropriate amount of catalyst is added to the reaction vessel. When this catalyst has high activity and selectivity, it can promote the reaction in the direction of generating the target product. Commonly used catalysts or metal complexes can effectively reduce the activation energy of the reaction and accelerate the reaction rate.
Then inject a suitable hydrogen source into it for the addition reaction of dihydrogen. The hydrogen source can be selected from common substances such as hydrogen. Before entering the reaction system, its purity must be ensured to prevent impurities from affecting the reaction process.
React under suitable temperature and pressure conditions. The regulation of temperature and pressure is extremely critical. Improper temperature and pressure conditions may cause the reaction rate to be too slow, or cause side reactions. Generally speaking, the temperature can be maintained in a specific range, such as between [X] ° C and [X] ° C, and the pressure is also controlled in the range of [X] MPa to [X] MPa. Under these conditions, the starting material reacts with a hydrogen source under the action of a catalyst to gradually generate 1% 2C3-dihydro-2- (hydromethyl) naphthalene.
After the reaction is completed, the reaction product is separated and purified. Common separation methods such as distillation, extraction, column chromatography, etc. can be used to obtain high-purity target products. After fine separation and purification operations, the desired 1% 2C3-dihydro-2- (hydromethyl) naphthalene can be obtained.
What are the precautions for the use of 1,3-dichloro-2- (chloromethyl) benzene?
1% 2C3 -dideuterium-2- (deuterium methyl) benzene should be used during the following matters:
First, this substance is chemically active. When operating, be sure to wear appropriate protective equipment, such as laboratory clothes, gloves, and goggles, to prevent it from coming into contact with the skin and eyes. If it comes into contact accidentally, rinse immediately with plenty of water and seek medical treatment in a timely manner.
Second, due to its special chemical properties, it is easy to react with other chemical substances. Therefore, in terms of storage, it should be placed in a dry, cool and well-ventilated place, away from fire sources, heat sources and strong oxidants, etc., and should be stored separately from other chemicals. Do not mix storage and transportation to avoid dangerous chemical reactions.
Third, when using, it should be operated in a place with good ventilation conditions, preferably in a fume hood, so as to effectively prevent its volatile gaseous substances from accumulating in the air, thereby avoiding damage to the human respiratory tract. At the same time, it can also reduce the possibility of dangerous accidents such as explosions.
Fourth, for the use of this substance, it must be carried out in strict accordance with accurate experimental procedures or production requirements, and the dosage must not be changed at will. When weighing, precise instruments should be used to ensure the accuracy and stability of the experiment or production.
Fifth, after use, the remaining 1% 2C3 -dideuterium-2- (deuteromethyl) benzene and related waste should be properly disposed of in accordance with the prescribed procedures, and must not be discarded at will to avoid pollution to the environment.
First, this substance is chemically active. When operating, be sure to wear appropriate protective equipment, such as laboratory clothes, gloves, and goggles, to prevent it from coming into contact with the skin and eyes. If it comes into contact accidentally, rinse immediately with plenty of water and seek medical treatment in a timely manner.
Second, due to its special chemical properties, it is easy to react with other chemical substances. Therefore, in terms of storage, it should be placed in a dry, cool and well-ventilated place, away from fire sources, heat sources and strong oxidants, etc., and should be stored separately from other chemicals. Do not mix storage and transportation to avoid dangerous chemical reactions.
Third, when using, it should be operated in a place with good ventilation conditions, preferably in a fume hood, so as to effectively prevent its volatile gaseous substances from accumulating in the air, thereby avoiding damage to the human respiratory tract. At the same time, it can also reduce the possibility of dangerous accidents such as explosions.
Fourth, for the use of this substance, it must be carried out in strict accordance with accurate experimental procedures or production requirements, and the dosage must not be changed at will. When weighing, precise instruments should be used to ensure the accuracy and stability of the experiment or production.
Fifth, after use, the remaining 1% 2C3 -dideuterium-2- (deuteromethyl) benzene and related waste should be properly disposed of in accordance with the prescribed procedures, and must not be discarded at will to avoid pollution to the environment.
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