Linshang Chemical
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1,4-Dichloro-2-(Chloromethyl)Benzene
Linshang Chemical
|
HS Code |
147763 |
| Chemical Formula | C7H5Cl3 |
| Molar Mass | 195.47 g/mol |
| Appearance | Solid (likely white or off - white) |
| Odor | Typical chlorinated benzene - like odor |
| Density | Data needed |
| Melting Point | Data needed |
| Boiling Point | Data needed |
| Solubility In Water | Low solubility |
| Solubility In Organic Solvents | Soluble in common organic solvents like benzene, toluene |
| Flash Point | Data needed |
| Vapor Pressure | Data needed |
| Stability | Stable under normal conditions, but reactive with strong oxidizing agents |
As an accredited 1,4-Dichloro-2-(Chloromethyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100 - gram bottles containing 1,4 - dichloro - 2-(chloromethyl)benzene, well - sealed. |
| Storage | 1,4 - Dichloro - 2-(chloromethyl)benzene should be stored in a cool, dry, well - ventilated area, away from sources of heat, ignition, and sunlight. It must be kept in a tightly - sealed container, preferably made of corrosion - resistant materials. Store it separately from oxidizing agents, acids, and bases to prevent potential chemical reactions. |
| Shipping | 1,4 - Dichloro - 2 - (chloromethyl)benzene is a chemical that requires careful shipping. It should be packaged in suitable, leak - proof containers, transported under proper temperature control, following all hazardous chemical shipping regulations to ensure safety. |
Competitive 1,4-Dichloro-2-(Chloromethyl)Benzene prices that fit your budget—flexible terms and customized quotes for every order.
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What are the chemical properties of 1,4-dichloro-2- (chloromethyl) benzene?
1% 2C4-dioxy-2- (methoxy) benzene, this substance has the following chemical properties:
First, it has ether bond stability. The dioxygen structure in the molecule is essentially an ether bond. The ether bond is generally chemically stable and is inert to many reagents. At room temperature, it is not easy to react with bases and dilute acids. In the field of organic synthesis, this property is often used as a protective group. After the reaction is completed, the protection is removed under specific conditions to retain the key structure and achieve specific synthesis goals.
Second, the benzene ring has electrophilic substitution activity. As an aromatic compound, the benzene ring is rich in electrons and exhibits typical electrophilic substitution reaction activity. It can react with electrophilic reagents such as halogens, nitrifiers, and sulfonating agents. For example, in the presence of catalysts such as ferric chloride, halogenation can occur with chlorine to form chlorine derivatives; under the action of a mixed system of concentrated sulfuric acid and concentrated nitric acid, nitrification can occur, and nitro groups are introduced into the benzene ring.
Third, methoxy groups affect the electron cloud density and reactivity of the benzene ring. Methoxy groups are the power supply sub-groups, and through their p-π conjugation effect, the electron cloud density of the benzene ring is increased, especially the electron cloud density of the ortho and para-sites is significantly increased. As a result, electrophilic substitution reactions are more likely to occur in the ortho and para-sites. For example, during bromination, bromine atoms mainly attack the ortho and para-sites of the methoxy group to generate corresponding bromogeneration products.
Fourth, decomposition or rearrangement may occur under Although the substance is usually relatively stable, under certain conditions such as heat or light, decomposition reactions may occur to generate small molecule products; or intramolecular rearrangements may occur, resulting in structural changes and the formation of new isomers.
First, it has ether bond stability. The dioxygen structure in the molecule is essentially an ether bond. The ether bond is generally chemically stable and is inert to many reagents. At room temperature, it is not easy to react with bases and dilute acids. In the field of organic synthesis, this property is often used as a protective group. After the reaction is completed, the protection is removed under specific conditions to retain the key structure and achieve specific synthesis goals.
Second, the benzene ring has electrophilic substitution activity. As an aromatic compound, the benzene ring is rich in electrons and exhibits typical electrophilic substitution reaction activity. It can react with electrophilic reagents such as halogens, nitrifiers, and sulfonating agents. For example, in the presence of catalysts such as ferric chloride, halogenation can occur with chlorine to form chlorine derivatives; under the action of a mixed system of concentrated sulfuric acid and concentrated nitric acid, nitrification can occur, and nitro groups are introduced into the benzene ring.
Third, methoxy groups affect the electron cloud density and reactivity of the benzene ring. Methoxy groups are the power supply sub-groups, and through their p-π conjugation effect, the electron cloud density of the benzene ring is increased, especially the electron cloud density of the ortho and para-sites is significantly increased. As a result, electrophilic substitution reactions are more likely to occur in the ortho and para-sites. For example, during bromination, bromine atoms mainly attack the ortho and para-sites of the methoxy group to generate corresponding bromogeneration products.
Fourth, decomposition or rearrangement may occur under Although the substance is usually relatively stable, under certain conditions such as heat or light, decomposition reactions may occur to generate small molecule products; or intramolecular rearrangements may occur, resulting in structural changes and the formation of new isomers.
What are the main uses of 1,4-dichloro-2- (chloromethyl) benzene?
1% 2C4-dioxy-2- (oxomethyl) furan, which has a wide range of uses. In the field of medicine, it can be used as a key intermediate to help synthesize a variety of drugs. For example, in the preparation of some antibacterial drugs, it can participate in specific reaction steps and play a key role in the construction of drug molecular structure and the endowment of activity.
In the field of organic synthesis, 1% 2C4-dioxy-2- (oxomethyl) furan can be used as a unique synthetic building block due to its unique chemical structure. Chemists use it to build various complex organic molecules, and through ingenious design of reaction paths, with the help of its activity check point, react with other organic reagents to construct organic compounds with specific functions and structures, providing a variety of possibilities for the development of organic synthetic chemistry.
It also has potential applications in materials science. With appropriate chemical modification and reaction, it can be integrated into some functional materials to improve the properties of materials, such as enhancing the stability and flexibility of materials or endowing materials with specific optical and electrical properties, opening up new directions for the research and development of new materials.
In the fragrance industry, it may contribute unique odor components. Due to its unique chemical structure, it can add a unique flavor to the fragrance, enrich the fragrance level, and play a role in the research and development of perfumes, food fragrances, and other products, giving the product a unique olfactory experience.
In the field of organic synthesis, 1% 2C4-dioxy-2- (oxomethyl) furan can be used as a unique synthetic building block due to its unique chemical structure. Chemists use it to build various complex organic molecules, and through ingenious design of reaction paths, with the help of its activity check point, react with other organic reagents to construct organic compounds with specific functions and structures, providing a variety of possibilities for the development of organic synthetic chemistry.
It also has potential applications in materials science. With appropriate chemical modification and reaction, it can be integrated into some functional materials to improve the properties of materials, such as enhancing the stability and flexibility of materials or endowing materials with specific optical and electrical properties, opening up new directions for the research and development of new materials.
In the fragrance industry, it may contribute unique odor components. Due to its unique chemical structure, it can add a unique flavor to the fragrance, enrich the fragrance level, and play a role in the research and development of perfumes, food fragrances, and other products, giving the product a unique olfactory experience.
What are the methods for preparing 1,4-dichloro-2- (chloromethyl) benzene?
The preparation method of 1% 2C4-dioxy-2- (oxomethyl) furan has various routes, which are described in detail below.
First, it can be achieved through a specific organic synthesis reaction path. With suitable starting materials, such as compounds containing specific functional groups, the target molecular structure is gradually constructed through carefully designed reaction steps. In this process, it is necessary to precisely control the reaction conditions, such as temperature, pressure, reaction time, and catalyst selection and dosage. Too high or too low temperature may cause the reaction to be biased towards side reactions, or the reaction rate may be too slow, making it difficult to achieve the expected yield. The regulation of pressure cannot be ignored. A specific reaction may require a specific pressure environment to promote the reaction to generate the target product. The catalyst can effectively reduce the activation energy of the reaction and speed up the reaction rate. However, the dosage must be carefully weighed. Too much or too little may have adverse effects on the reaction.
Second, biosynthesis is also one way to prepare this compound. With the help of microorganisms or enzymes, the synthesis of the target product is achieved under relatively mild conditions. Biocatalysis is highly selective and specific, which can reduce the occurrence of side reactions, and usually the reaction conditions are more green and environmentally friendly, which is in line with the concept of sustainable development. However, biosynthesis also faces many challenges, such as the harsh culture conditions of microorganisms, the stability and activity of enzymes are easily affected by external factors, and the culture environment and reaction system need to be carefully regulated to ensure the efficient progress of biocatalytic reactions.
Third, natural product extraction. If there are biological resources rich in this compound or its precursors in nature, the target product can be obtained through appropriate extraction and separation techniques. The key to this method is to find suitable natural resources and optimize the extraction and separation process. Different natural resources contain different amounts and forms of target compounds, so it is necessary to select the extraction solvent, extraction method (such as extraction, distillation, etc.) and separation and purification means (such as column chromatography, high performance liquid chromatography, etc.) to obtain high-purity 1% 2C4-dioxy-2- (oxomethyl) furan.
First, it can be achieved through a specific organic synthesis reaction path. With suitable starting materials, such as compounds containing specific functional groups, the target molecular structure is gradually constructed through carefully designed reaction steps. In this process, it is necessary to precisely control the reaction conditions, such as temperature, pressure, reaction time, and catalyst selection and dosage. Too high or too low temperature may cause the reaction to be biased towards side reactions, or the reaction rate may be too slow, making it difficult to achieve the expected yield. The regulation of pressure cannot be ignored. A specific reaction may require a specific pressure environment to promote the reaction to generate the target product. The catalyst can effectively reduce the activation energy of the reaction and speed up the reaction rate. However, the dosage must be carefully weighed. Too much or too little may have adverse effects on the reaction.
Second, biosynthesis is also one way to prepare this compound. With the help of microorganisms or enzymes, the synthesis of the target product is achieved under relatively mild conditions. Biocatalysis is highly selective and specific, which can reduce the occurrence of side reactions, and usually the reaction conditions are more green and environmentally friendly, which is in line with the concept of sustainable development. However, biosynthesis also faces many challenges, such as the harsh culture conditions of microorganisms, the stability and activity of enzymes are easily affected by external factors, and the culture environment and reaction system need to be carefully regulated to ensure the efficient progress of biocatalytic reactions.
Third, natural product extraction. If there are biological resources rich in this compound or its precursors in nature, the target product can be obtained through appropriate extraction and separation techniques. The key to this method is to find suitable natural resources and optimize the extraction and separation process. Different natural resources contain different amounts and forms of target compounds, so it is necessary to select the extraction solvent, extraction method (such as extraction, distillation, etc.) and separation and purification means (such as column chromatography, high performance liquid chromatography, etc.) to obtain high-purity 1% 2C4-dioxy-2- (oxomethyl) furan.
What are the precautions for the use of 1,4-dichloro-2- (chloromethyl) benzene?
When using 1% 2C4-dioxy-2- (oxomethyl) ether, there are various things that should be paid attention to. The details are as follows:
bear the brunt of it, and it is safe to be serious. This substance is toxic and irritating, and it is necessary to strictly follow safety procedures when taking it. Before starting the operation, prepare suitable protective equipment, such as protective gloves, goggles, gas masks, etc., to protect yourself from direct contact with the skin and eyes, and to prevent inhalation of its volatile aerosol. If you accidentally touch it, rinse it with plenty of water immediately, and then go to the medical office for treatment.
Second time, be careful when storing. It should be stored in a cool, dry and well-ventilated place, away from fire and heat sources, and away from direct sunlight. At the same time, it should be stored separately from oxidants, acids, alkalis, etc., and should not be mixed to prevent dangerous chemical reactions. The storage area should be equipped with suitable materials to contain leaks.
Furthermore, when using, the operation should be careful. It should be carried out in a fume hood to ensure smooth air circulation and reduce the risk of accumulation of harmful substances. Accurately control the dosage, do not exceed the required amount. After the operation, clean the utensils and site in time to prevent residual substances from causing pollution or accidents.
Repeat, when transporting, it should not be ignored. It needs to be properly packaged in accordance with relevant regulations and clearly marked to ensure that it is stable during transportation, avoid collision, dumping, and prevent leakage.
In general, when using 1% 2C4-dioxy-2- (oxomethyl) ether, all steps must be taken with care to ensure the safety of personnel and the environment.
bear the brunt of it, and it is safe to be serious. This substance is toxic and irritating, and it is necessary to strictly follow safety procedures when taking it. Before starting the operation, prepare suitable protective equipment, such as protective gloves, goggles, gas masks, etc., to protect yourself from direct contact with the skin and eyes, and to prevent inhalation of its volatile aerosol. If you accidentally touch it, rinse it with plenty of water immediately, and then go to the medical office for treatment.
Second time, be careful when storing. It should be stored in a cool, dry and well-ventilated place, away from fire and heat sources, and away from direct sunlight. At the same time, it should be stored separately from oxidants, acids, alkalis, etc., and should not be mixed to prevent dangerous chemical reactions. The storage area should be equipped with suitable materials to contain leaks.
Furthermore, when using, the operation should be careful. It should be carried out in a fume hood to ensure smooth air circulation and reduce the risk of accumulation of harmful substances. Accurately control the dosage, do not exceed the required amount. After the operation, clean the utensils and site in time to prevent residual substances from causing pollution or accidents.
Repeat, when transporting, it should not be ignored. It needs to be properly packaged in accordance with relevant regulations and clearly marked to ensure that it is stable during transportation, avoid collision, dumping, and prevent leakage.
In general, when using 1% 2C4-dioxy-2- (oxomethyl) ether, all steps must be taken with care to ensure the safety of personnel and the environment.
What are the environmental effects of 1,4-dichloro-2- (chloromethyl) benzene?
1% 2C4-dioxy-2- (oxomethyl) furan is particularly important for its environmental impact. It has a special chemical structure and can cause diverse effects among environmental media such as atmosphere, water and soil.
First of all, in the atmospheric environment, 1% 2C4-dioxy-2- (oxomethyl) furan may escape into the atmosphere due to volatilization. It reacts with free radicals such as hydroxyl radicals in the atmosphere. This reaction may promote its degradation, but other secondary pollutants may be produced during the degradation process. If it is under light conditions, or through photochemical reactions, it further generates harmful pollutants such as ozone, causing deterioration of air quality, and may damage the atmospheric ozone layer, affecting the earth's ultraviolet shielding function.
As for the water environment, if 1% 2C4-dioxo-2- (oxomethyl) furan enters the water body, it may have certain solubility due to its chemical properties. This can affect the chemical composition of the water body, change the pH and redox potential of the water body. And it may have toxic effects on aquatic organisms and interfere with the physiological metabolic process of aquatic organisms. Aquatic organisms such as fish and algae may be exposed to this substance, causing growth and development to be hindered, reproductive capacity to decline, and even death, ultimately breaking the balance of aquatic ecosystems.
The soil environment is also affected by it. After 1% 2C4-dioxy-2- (oxomethyl) furan enters the soil, it may be adsorbed on the surface of soil particles, affecting the physical and chemical properties of the soil. It may change the pore structure of the soil, affecting the aeration and water permeability of the soil. And it may affect the soil microbial community, inhibit or promote the growth and metabolism of certain microorganisms, and then affect the material cycle and energy conversion process of the soil. If it accumulates in the soil or is absorbed by plant roots and enters the food chain, it poses a potential threat to the terrestrial ecosystem.
In summary, the impact of 1% 2C4-dioxy-2- (oxomethyl) furan on the environment is extensive and complex, which is related to the ecological fields of atmosphere, water and soil, and cannot be ignored.
First of all, in the atmospheric environment, 1% 2C4-dioxy-2- (oxomethyl) furan may escape into the atmosphere due to volatilization. It reacts with free radicals such as hydroxyl radicals in the atmosphere. This reaction may promote its degradation, but other secondary pollutants may be produced during the degradation process. If it is under light conditions, or through photochemical reactions, it further generates harmful pollutants such as ozone, causing deterioration of air quality, and may damage the atmospheric ozone layer, affecting the earth's ultraviolet shielding function.
As for the water environment, if 1% 2C4-dioxo-2- (oxomethyl) furan enters the water body, it may have certain solubility due to its chemical properties. This can affect the chemical composition of the water body, change the pH and redox potential of the water body. And it may have toxic effects on aquatic organisms and interfere with the physiological metabolic process of aquatic organisms. Aquatic organisms such as fish and algae may be exposed to this substance, causing growth and development to be hindered, reproductive capacity to decline, and even death, ultimately breaking the balance of aquatic ecosystems.
The soil environment is also affected by it. After 1% 2C4-dioxy-2- (oxomethyl) furan enters the soil, it may be adsorbed on the surface of soil particles, affecting the physical and chemical properties of the soil. It may change the pore structure of the soil, affecting the aeration and water permeability of the soil. And it may affect the soil microbial community, inhibit or promote the growth and metabolism of certain microorganisms, and then affect the material cycle and energy conversion process of the soil. If it accumulates in the soil or is absorbed by plant roots and enters the food chain, it poses a potential threat to the terrestrial ecosystem.
In summary, the impact of 1% 2C4-dioxy-2- (oxomethyl) furan on the environment is extensive and complex, which is related to the ecological fields of atmosphere, water and soil, and cannot be ignored.
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