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2-(4-Ethoxybenzyl)-4-Bromo-1-Chlorobenzene
Linshang Chemical
|
HS Code |
141964 |
| Chemical Formula | C15H14BrClO |
| Molecular Weight | 327.63 |
| Appearance | Solid (usually) |
| Melting Point | Data may vary depending on purity |
| Boiling Point | Data may vary depending on purity |
| Solubility In Water | Low solubility |
| Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, chloroform |
| Density | Data may vary depending on conditions |
| Flash Point | Data may vary depending on purity |
| Stability | Stable under normal conditions, but avoid heat, light, and strong oxidizing agents |
As an accredited 2-(4-Ethoxybenzyl)-4-Bromo-1-Chlorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 2-(4 - ethoxybenzyl)-4 - bromo - 1 - chlorobenzene packaged in a sealed glass bottle. |
| Storage | Store 2-(4 - ethoxybenzyl)-4 - bromo - 1 - chlorobenzene in a cool, dry, well - ventilated area away from sources of heat, ignition, and incompatible substances. Keep it in a tightly sealed container, preferably made of corrosion - resistant material. Avoid exposure to sunlight and moisture as they may cause degradation. Label the storage container clearly for easy identification. |
| Shipping | 2-(4 - ethoxybenzyl)-4 - bromo - 1 - chlorobenzene is shipped in well - sealed containers, compliant with chemical transport regulations. Packaging ensures protection from physical damage and environmental exposure during transit. |
Competitive 2-(4-Ethoxybenzyl)-4-Bromo-1-Chlorobenzene 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
Where to Buy 2-(4-Ethoxybenzyl)-4-Bromo-1-Chlorobenzene in China?
As a trusted 2-(4-Ethoxybenzyl)-4-Bromo-1-Chlorobenzene manufacturer, we deliver:
Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements.
Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery.
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 2-(4-Ethoxybenzyl)-4-Bromo-1-Chlorobenzene 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 2- (4-ethoxybenzyl) -4-bromo-1-chlorobenzene?
2- (4-Acetoxybenzyl) -4-ether-1-bromonaphthalene has a wide range of main uses.
In the field of medicine, it can be used as a key intermediate. Through specific chemical reactions and modifications, compounds with unique pharmacological activities can be synthesized. Or the development of therapeutic drugs for certain diseases is very helpful. For example, in the development of anti-tumor drugs, its structure can be modified to combine with specific targets of tumor cells, inhibit the proliferation of tumor cells, and then provide a new direction for solving tumor problems.
In the field of materials science, it also shows potential value. Due to the special properties given by the unique chemical structure, it can participate in the construction of high-performance materials. For example, in organic photoelectric materials, it can optimize the photoelectric conversion efficiency of the material, so that the performance of related photoelectric devices, such as organic Light Emitting Diode (OLED), solar cells, etc. can be improved, so that the OLED screen display is clearer, the color is brighter, and the photoelectric conversion of solar cells is more efficient, promoting the development of related industries.
In the field of fine chemicals, it is also an indispensable raw material. It can be used to synthesize various fine chemicals, such as special fragrances, high-end paint additives, etc. Add a unique aroma level to the fragrance, or improve the weather resistance, adhesion and other properties of the paint, to meet the high-quality needs of fine chemicals in different industries.
In summary, 2- (4-acetoxybenzyl) -4-ether-1-bromonaphthalene has critical uses in many important fields, which is of great significance for promoting technological progress and product upgrades in various fields.
In the field of medicine, it can be used as a key intermediate. Through specific chemical reactions and modifications, compounds with unique pharmacological activities can be synthesized. Or the development of therapeutic drugs for certain diseases is very helpful. For example, in the development of anti-tumor drugs, its structure can be modified to combine with specific targets of tumor cells, inhibit the proliferation of tumor cells, and then provide a new direction for solving tumor problems.
In the field of materials science, it also shows potential value. Due to the special properties given by the unique chemical structure, it can participate in the construction of high-performance materials. For example, in organic photoelectric materials, it can optimize the photoelectric conversion efficiency of the material, so that the performance of related photoelectric devices, such as organic Light Emitting Diode (OLED), solar cells, etc. can be improved, so that the OLED screen display is clearer, the color is brighter, and the photoelectric conversion of solar cells is more efficient, promoting the development of related industries.
In the field of fine chemicals, it is also an indispensable raw material. It can be used to synthesize various fine chemicals, such as special fragrances, high-end paint additives, etc. Add a unique aroma level to the fragrance, or improve the weather resistance, adhesion and other properties of the paint, to meet the high-quality needs of fine chemicals in different industries.
In summary, 2- (4-acetoxybenzyl) -4-ether-1-bromonaphthalene has critical uses in many important fields, which is of great significance for promoting technological progress and product upgrades in various fields.
What are the physical properties of 2- (4-ethoxybenzyl) -4-bromo-1-chlorobenzene?
2-%284-%E4%B9%99%E6%B0%A7%E5%9F%BA%E8%8B%84%E5%9F%BA%29-4-%E6%BA%B4-1-%E6%B0%AF%E8%8B%AF%E7%9A%84%E7%89%A9%E7%90%86%E6%80%A7%E8%B4%A8%E5%88%97%E8%A1%A8%E5%A6%82%E4%B8%8B%EF%BC%9A
2- (4-ethylhydroxybenzyl) -4-ether-1-chloronaphthalene physical properties
1. ** External properties **: This compound is often solid, or white to light crystalline powder. The reason why it is solid is that the molecular force is sufficient to hold a certain lattice. In addition, it is advantageous for the storage of water under normal conditions, and the reaction is reversed in the process, which can be easily used.
2. ** Melting temperature **: Melting temperature is at [X] ℃, and the boiling temperature is at [X] ℃. The specific value of the melting temperature depends on the interaction of molecules, including the temperature, van der force, etc. The high melting temperature of the phase indicates that the molecular force is high. The value of the melting temperature depends on its physical performance in different temperature environments, as well as operations such as lifting and dividing.
3. ** Density **: Density is [X] g/cm ³. Density is a physical property, reflecting the amount of material in the temperature position. When it comes to mixing, dissolution, etc., the density can be used to calculate the amount of material, and the ratio of materials in chemical production is especially important.
4. ** Solubility **: It has a certain solubility in soluble substances such as ethanol and acetone, but its solubility in water is low. It is due to the fact that it contains a large number of hydrophobic groups in its molecules, making it more susceptible to soluble interactions. In chemical synthesis, its solubility characteristics can be used, and it is suitable for dissolution.
5. ** Qualitative **: Under normal conditions and general environmental conditions, it has a certain degree of characterization. However, if exposed to specific substances such as oxidation, high temperature or light, it may be biochemically reactive. The chemical energy in the qualitative molecule, molecular cloud separation and other factors are related. Understanding its characterization is an important reference for the storage of the material and the attention in the use process.
2- (4-ethylhydroxybenzyl) -4-ether-1-chloronaphthalene physical properties
1. ** External properties **: This compound is often solid, or white to light crystalline powder. The reason why it is solid is that the molecular force is sufficient to hold a certain lattice. In addition, it is advantageous for the storage of water under normal conditions, and the reaction is reversed in the process, which can be easily used.
2. ** Melting temperature **: Melting temperature is at [X] ℃, and the boiling temperature is at [X] ℃. The specific value of the melting temperature depends on the interaction of molecules, including the temperature, van der force, etc. The high melting temperature of the phase indicates that the molecular force is high. The value of the melting temperature depends on its physical performance in different temperature environments, as well as operations such as lifting and dividing.
3. ** Density **: Density is [X] g/cm ³. Density is a physical property, reflecting the amount of material in the temperature position. When it comes to mixing, dissolution, etc., the density can be used to calculate the amount of material, and the ratio of materials in chemical production is especially important.
4. ** Solubility **: It has a certain solubility in soluble substances such as ethanol and acetone, but its solubility in water is low. It is due to the fact that it contains a large number of hydrophobic groups in its molecules, making it more susceptible to soluble interactions. In chemical synthesis, its solubility characteristics can be used, and it is suitable for dissolution.
5. ** Qualitative **: Under normal conditions and general environmental conditions, it has a certain degree of characterization. However, if exposed to specific substances such as oxidation, high temperature or light, it may be biochemically reactive. The chemical energy in the qualitative molecule, molecular cloud separation and other factors are related. Understanding its characterization is an important reference for the storage of the material and the attention in the use process.
What is the synthesis method of 2- (4-ethoxybenzyl) -4-bromo-1-chlorobenzene?
To prepare 2- (4-hydroxyethylpiperazine) - 4-chloro-1-fluorobenzene, the following ancient method can be used.
First, appropriate raw materials are taken, and they are obtained by organic synthesis through several steps. The choice of starting materials is quite critical, and corresponding functional groups are required to facilitate subsequent reaction advancement.
In the first step, fluorinated benzene compounds and chlorine-containing reagents can be substituted under specific reaction conditions, such as in a suitable catalyst, temperature and solvent environment. This reaction aims to introduce chlorine atoms into the benzene ring to form benzene derivatives containing fluorine and chlorine. The catalyst used should be carefully selected according to the reaction mechanism and substrate characteristics, and the temperature should be precisely controlled. Too high or too low can affect the rate and yield of the reaction.
In the next step, 4-hydroxyethylpiperazine can be prepared. It can be obtained by reacting piperazine with ethylene oxide in a suitable reaction system. In this process, the reaction ratio of materials and reaction time must be properly considered to ensure the purity and yield of the product.
Then, the 4-hydroxyethylpiperazine obtained in the previous step is reacted with the benzene derivative that has been introduced into chlorine and fluorine. This reaction may require an alkaline environment to promote the reaction, so that the nitrogen atom of piperazine reacts with the appropriate position on the benzene ring, and then constructs the basic structure of the target product.
After each step of the reaction, the separation and purification operation should be carried out. The commonly used methods such as recrystallization and column chromatography can be used to remove impurities and improve the purity of the product. And in the whole synthesis process, the reaction process needs to be closely monitored, and the analysis methods such as thin-layer chromatography and nuclear magnetic resonance can be used to ensure that the reaction proceeds in the expected direction, and finally the pure 2- (4-hydroxyethylpiperazine) - 4-chloro-1-fluorobenzene is obtained.
First, appropriate raw materials are taken, and they are obtained by organic synthesis through several steps. The choice of starting materials is quite critical, and corresponding functional groups are required to facilitate subsequent reaction advancement.
In the first step, fluorinated benzene compounds and chlorine-containing reagents can be substituted under specific reaction conditions, such as in a suitable catalyst, temperature and solvent environment. This reaction aims to introduce chlorine atoms into the benzene ring to form benzene derivatives containing fluorine and chlorine. The catalyst used should be carefully selected according to the reaction mechanism and substrate characteristics, and the temperature should be precisely controlled. Too high or too low can affect the rate and yield of the reaction.
In the next step, 4-hydroxyethylpiperazine can be prepared. It can be obtained by reacting piperazine with ethylene oxide in a suitable reaction system. In this process, the reaction ratio of materials and reaction time must be properly considered to ensure the purity and yield of the product.
Then, the 4-hydroxyethylpiperazine obtained in the previous step is reacted with the benzene derivative that has been introduced into chlorine and fluorine. This reaction may require an alkaline environment to promote the reaction, so that the nitrogen atom of piperazine reacts with the appropriate position on the benzene ring, and then constructs the basic structure of the target product.
After each step of the reaction, the separation and purification operation should be carried out. The commonly used methods such as recrystallization and column chromatography can be used to remove impurities and improve the purity of the product. And in the whole synthesis process, the reaction process needs to be closely monitored, and the analysis methods such as thin-layer chromatography and nuclear magnetic resonance can be used to ensure that the reaction proceeds in the expected direction, and finally the pure 2- (4-hydroxyethylpiperazine) - 4-chloro-1-fluorobenzene is obtained.
What should be paid attention to when storing 2- (4-ethoxybenzyl) -4-bromo-1-chlorobenzene?
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First, all these things need to be properly placed to prevent damage. 2 - (4 - ethyl hydroxyurea) - 4 - ether - 1 - chloronaphthalene is more active, and it is easy to change when exposed to light, heat, and humidity. Therefore, the storage place should be a cool, dry, well-ventilated place, away from direct sunlight and hot topic environments.
Furthermore, these chemicals are more toxic and corrosive. When storing, they must be separated from other items, especially flammable, explosive, and oxidizing materials, and must not be mixed to avoid accidental violent reactions. And the container must be firmly sealed to prevent leakage. If there is a leak, it will be a big disaster, or cause environmental pollution and endanger the health of humans and animals.
In addition, the storage place should be clearly marked, stating the name of the object, characteristics, hazards and emergency measures, etc., so that the relevant people can understand at a glance, and can respond quickly in case of emergencies. Periodically, people should also be sent to check whether the container is damaged or abnormal. If there is any problem, deal with it immediately to ensure safety. During the process of access and storage, the person involved must strictly abide by the operating procedures and adapt protective equipment, such as gloves, goggles, protective clothing, etc., to protect their own safety.
First, all these things need to be properly placed to prevent damage. 2 - (4 - ethyl hydroxyurea) - 4 - ether - 1 - chloronaphthalene is more active, and it is easy to change when exposed to light, heat, and humidity. Therefore, the storage place should be a cool, dry, well-ventilated place, away from direct sunlight and hot topic environments.
Furthermore, these chemicals are more toxic and corrosive. When storing, they must be separated from other items, especially flammable, explosive, and oxidizing materials, and must not be mixed to avoid accidental violent reactions. And the container must be firmly sealed to prevent leakage. If there is a leak, it will be a big disaster, or cause environmental pollution and endanger the health of humans and animals.
In addition, the storage place should be clearly marked, stating the name of the object, characteristics, hazards and emergency measures, etc., so that the relevant people can understand at a glance, and can respond quickly in case of emergencies. Periodically, people should also be sent to check whether the container is damaged or abnormal. If there is any problem, deal with it immediately to ensure safety. During the process of access and storage, the person involved must strictly abide by the operating procedures and adapt protective equipment, such as gloves, goggles, protective clothing, etc., to protect their own safety.
What are the environmental effects of 2- (4-ethoxybenzyl) -4-bromo-1-chlorobenzene?
Fu 2 - (4 -ethoxyphenyl) - 4 -aldehyde-1 -bromonaphthalene is involved in the environment and is related to the impact of chemical substances on the surrounding ecology.
The structure of this compound involves the coexistence of ethoxyphenyl, aldehyde and bromonaphthalene. The aldehyde group has active chemical properties and can be involved in various reactions such as oxidation, reduction, and condensation. In the natural environment, its structure may be modified due to microbial action, light, oxidation and other factors.
In terms of self-microbial degradation, various microorganisms in the environment can use the action of enzymes to decompose and metabolize the compound. However, the presence of bromonaphthalene in its structure may make it difficult for microorganisms to degrade. The introduction of bromine atoms can improve the stability of molecules, and the electron clouds around bromine atoms are different, making it difficult for microbial enzymes to act on the structure, delaying the degradation process, or causing it to remain in the environment.
Under light, this compound may have a photochemical reaction. The aldehyde group is sensitive to light, and when illuminated, it can stimulate electron transitions, cause chemical bonds to break or rearrange, and generate new chemicals. This new biomass may have higher activity and toxicity, causing damage to cells, tissues or organisms in the environment, such as interfering with normal metabolic pathways in organisms and destroying the integrity of cell membranes.
Furthermore, the migration and transformation of the compound in water, soil and other media is also important. Its water solubility or low, it is easy to adsorb suspended particles in water bodies, migrate to other places with water flow, and deposit in sediment after sedimentation. In soil, or interact with organic matter and minerals on the surface of soil particles, affecting its diffusion in soil pores, and then affecting its bioavailability.
In conclusion, the potential impact of 2 - (4-ethoxyphenyl) - 4-aldehyde-1-bromonaphthalene on the ecological environment due to its own structural characteristics in terms of microbial degradation, light reaction and medium migration and transformation should be carefully considered.
The structure of this compound involves the coexistence of ethoxyphenyl, aldehyde and bromonaphthalene. The aldehyde group has active chemical properties and can be involved in various reactions such as oxidation, reduction, and condensation. In the natural environment, its structure may be modified due to microbial action, light, oxidation and other factors.
In terms of self-microbial degradation, various microorganisms in the environment can use the action of enzymes to decompose and metabolize the compound. However, the presence of bromonaphthalene in its structure may make it difficult for microorganisms to degrade. The introduction of bromine atoms can improve the stability of molecules, and the electron clouds around bromine atoms are different, making it difficult for microbial enzymes to act on the structure, delaying the degradation process, or causing it to remain in the environment.
Under light, this compound may have a photochemical reaction. The aldehyde group is sensitive to light, and when illuminated, it can stimulate electron transitions, cause chemical bonds to break or rearrange, and generate new chemicals. This new biomass may have higher activity and toxicity, causing damage to cells, tissues or organisms in the environment, such as interfering with normal metabolic pathways in organisms and destroying the integrity of cell membranes.
Furthermore, the migration and transformation of the compound in water, soil and other media is also important. Its water solubility or low, it is easy to adsorb suspended particles in water bodies, migrate to other places with water flow, and deposit in sediment after sedimentation. In soil, or interact with organic matter and minerals on the surface of soil particles, affecting its diffusion in soil pores, and then affecting its bioavailability.
In conclusion, the potential impact of 2 - (4-ethoxyphenyl) - 4-aldehyde-1-bromonaphthalene on the ecological environment due to its own structural characteristics in terms of microbial degradation, light reaction and medium migration and transformation should be carefully considered.
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