Linshang Chemical
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2-Bromo-1,3,5-Trichlorobenzene
Linshang Chemical
|
HS Code |
840526 |
| Chemical Formula | C6H2BrCl3 |
| Molar Mass | 272.34 g/mol |
| Appearance | Solid |
| Color | Colorless to pale yellow |
| Odor | Pungent |
| Density | 1.92 g/cm³ |
| Melting Point | 52 - 54 °C |
| Boiling Point | 247 - 248 °C |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in many organic solvents like benzene, toluene |
As an accredited 2-Bromo-1,3,5-Trichlorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 2 - bromo - 1,3,5 - trichlorobenzene packaged in a sealed glass bottle. |
| Storage | 2 - bromo - 1,3,5 - trichlorobenzene should be stored in a cool, dry, well - ventilated area, away from sources of heat and ignition. Keep it in a tightly - sealed container to prevent leakage. Store it separately from oxidizing agents, reducing agents, and substances with which it may react. Follow local regulations for proper chemical storage. |
| Shipping | 2 - bromo - 1,3,5 - trichlorobenzene is shipped in well - sealed, corrosion - resistant containers. It follows strict hazardous material regulations, ensuring secure transportation to prevent any leakage or environmental and safety risks. |
Competitive 2-Bromo-1,3,5-Trichlorobenzene 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 2-Bromo-1,3,5-Trichlorobenzene 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 chemical properties of 2-bromo-1,3,5-trichlorobenzene?
2-% cyanogen-1,3,5-trichlorobenzene is also an organic compound. It has unique chemical properties, among which samadhi, let me explain in detail for you.
First of all, its chemical activity is quite significant. The presence of cyanyl groups makes this compound have a certain reactivity. Cyanyl groups can participate in many chemical reactions, such as nucleophilic substitution reactions. Under appropriate conditions, cyanyl groups can react with nucleophiles to introduce new functional groups, which is of great significance in the field of organic synthesis and can provide key intermediates for the preparation of various complex organic compounds.
Furthermore, halogen atoms (chlorine atoms) also give it special properties. The chlorine atoms in the structure of 1,3,5-trichlorobenzene can undergo substitution reactions. Due to the tendency of chlorine atoms to leave, in suitable reaction environments, such as alkaline conditions and the presence of nucleophiles, chlorine atoms can be replaced by other groups to form organic compounds with different structures and functions. At the same time, the electronegativity of chlorine atoms is relatively large, and its existence will affect the electron cloud distribution of molecules, which in turn will affect the physical and chemical properties of molecules, such as the polarity of molecules.
In addition, the stability of 2-% cyanogen-1,3,5-trichlorobenzene also has characteristics. Although cyanide and chlorine atoms give it certain reactivity, its structure is relatively stable under generally mild conditions. However, when it is in an environment of high temperature, strong acid and alkali, or the presence of specific catalysts, its chemical activity will be revealed, and various chemical reactions will occur to adapt to environmental changes.
In summary, the chemical properties of 2-% cyanogen-1,3,5-trichlorobenzene are determined by the synergistic effect of cyanyl groups and chlorine atoms. The balance of its reactivity and stability makes it an important location and potential application value in organic chemistry research and industrial production.
First of all, its chemical activity is quite significant. The presence of cyanyl groups makes this compound have a certain reactivity. Cyanyl groups can participate in many chemical reactions, such as nucleophilic substitution reactions. Under appropriate conditions, cyanyl groups can react with nucleophiles to introduce new functional groups, which is of great significance in the field of organic synthesis and can provide key intermediates for the preparation of various complex organic compounds.
Furthermore, halogen atoms (chlorine atoms) also give it special properties. The chlorine atoms in the structure of 1,3,5-trichlorobenzene can undergo substitution reactions. Due to the tendency of chlorine atoms to leave, in suitable reaction environments, such as alkaline conditions and the presence of nucleophiles, chlorine atoms can be replaced by other groups to form organic compounds with different structures and functions. At the same time, the electronegativity of chlorine atoms is relatively large, and its existence will affect the electron cloud distribution of molecules, which in turn will affect the physical and chemical properties of molecules, such as the polarity of molecules.
In addition, the stability of 2-% cyanogen-1,3,5-trichlorobenzene also has characteristics. Although cyanide and chlorine atoms give it certain reactivity, its structure is relatively stable under generally mild conditions. However, when it is in an environment of high temperature, strong acid and alkali, or the presence of specific catalysts, its chemical activity will be revealed, and various chemical reactions will occur to adapt to environmental changes.
In summary, the chemical properties of 2-% cyanogen-1,3,5-trichlorobenzene are determined by the synergistic effect of cyanyl groups and chlorine atoms. The balance of its reactivity and stability makes it an important location and potential application value in organic chemistry research and industrial production.
What are the main uses of 2-bromo-1,3,5-trichlorobenzene?
2-% cyanogen-1,3,5-tribromobenzene is an organic compound, which has significant functions in chemical synthesis and other fields. Although it is not directly described in "Tiangong Kaiwu", it can be inferred that such compounds may be involved in related processes according to the evolution of chemical technology and the application of materials at that time. The following are its main uses:
First, organic synthesis raw materials. 2-% cyanogen-1,3,5-tribromobenzene is rich in bromine atoms and cyano groups, which are all active reaction check points. Bromine atoms can be introduced into various functional groups through nucleophilic substitution reactions, such as reacting with alcohols and amines to form ether and amine derivatives. Cyanyl groups can be hydrolyzed into carboxyl groups or reduced to amino groups, thereby constructing complex organic molecular structures. It is often used as a key intermediate in the synthesis of drugs and dyes, helping to create novel structural compounds and expand the boundaries of synthetic chemistry.
Second, materials science applications. Due to its special chemical structure, it can participate in the construction of polymer materials. For example, as a comonomer, it can be polymerized with other monomers to give materials special properties, such as improving material thermal stability and flame retardancy. In the field of electronic materials, it can be used to prepare functional materials with specific electrical properties to meet the strict requirements of electronic components on material properties.
Third, potential value in agricultural chemistry. Some bromine and cyanyl compounds have biological activities. 2-% cyanogen-1,3,5-tribromobenzene can be rationally modified and modified, or can be developed into new pesticides, such as insecticides and fungicides. With its unique chemical structure, it can inhibit and kill specific pests and bacteria, and contribute to new ways for agricultural pest control.
Fourth, the research direction of medicinal chemistry. In the process of drug development, the structure of 2-% cyanogen-1,3,5-tribromobenzene can be used as a template for lead compounds. Medicinal chemists explore potential drug molecules with biological activity and suitable pharmacokinetic properties by modifying and optimizing their structures, providing an opportunity for the birth of innovative drugs and playing an important role in the development of drugs to overcome difficult diseases.
First, organic synthesis raw materials. 2-% cyanogen-1,3,5-tribromobenzene is rich in bromine atoms and cyano groups, which are all active reaction check points. Bromine atoms can be introduced into various functional groups through nucleophilic substitution reactions, such as reacting with alcohols and amines to form ether and amine derivatives. Cyanyl groups can be hydrolyzed into carboxyl groups or reduced to amino groups, thereby constructing complex organic molecular structures. It is often used as a key intermediate in the synthesis of drugs and dyes, helping to create novel structural compounds and expand the boundaries of synthetic chemistry.
Second, materials science applications. Due to its special chemical structure, it can participate in the construction of polymer materials. For example, as a comonomer, it can be polymerized with other monomers to give materials special properties, such as improving material thermal stability and flame retardancy. In the field of electronic materials, it can be used to prepare functional materials with specific electrical properties to meet the strict requirements of electronic components on material properties.
Third, potential value in agricultural chemistry. Some bromine and cyanyl compounds have biological activities. 2-% cyanogen-1,3,5-tribromobenzene can be rationally modified and modified, or can be developed into new pesticides, such as insecticides and fungicides. With its unique chemical structure, it can inhibit and kill specific pests and bacteria, and contribute to new ways for agricultural pest control.
Fourth, the research direction of medicinal chemistry. In the process of drug development, the structure of 2-% cyanogen-1,3,5-tribromobenzene can be used as a template for lead compounds. Medicinal chemists explore potential drug molecules with biological activity and suitable pharmacokinetic properties by modifying and optimizing their structures, providing an opportunity for the birth of innovative drugs and playing an important role in the development of drugs to overcome difficult diseases.
What are the synthesis methods of 2-bromo-1,3,5-trichlorobenzene?
There are several methods for the synthesis of 2-% hydrazine-1,3,5-trifluorobenzene. One method is to first take 1,3,5-trifluorobenzene and react with appropriate reagents to introduce hydrazine groups. This may be achieved by nucleophilic substitution. The fluorine atom of 1,3,5-trifluorobenzene is quite active and can interact with nucleophiles containing hydrazine groups.
To perform this nucleophilic substitution, suitable reaction conditions need to be selected. The choice of solvent is crucial. Polar aprotic solvents such as dimethyl sulfoxide (DMSO), N, N-dimethylformamide (DMF), etc. are often used. These solvents can improve the solubility and activity of nucleophiles without adverse effects on the reaction process.
The reaction temperature also needs to be fine-tuned. If it is too low, the reaction rate will be slow and take a long time; if it is too high, it may cause side reactions and lead to impure products. Generally speaking, moderate heating can speed up the reaction rate, but it needs to be controlled within a certain range, or between room temperature and moderate heating.
There is another method, which can first prepare an intermediate containing a hydrazine group, and then connect it with 1,3,5-trifluorobenzene through a specific reaction. The preparation of this intermediate can be achieved by means of functional group conversion and condensation according to the existing organic synthesis method. After the intermediate is ready, it is reacted with 1,3,5-trifluorobenzene under suitable conditions to obtain the target product 2-hydrazine-1,3,5-trifluorobenzene.
Furthermore, the catalytic reaction method may also be feasible. Selecting a suitable catalyst can promote the reaction, improve the selectivity and yield of the reaction. Some transition metal catalysts can effectively catalyze the reaction of hydrazine-containing reagents with 1,3,5-trifluorobenzene in specific organic reactions, making the reaction more efficient and specific. However, when using catalysts, it is necessary to consider their cost, activity and requirements for reaction conditions in order to achieve the best synthesis effect. All synthesis methods have advantages and disadvantages, and they need to be selected according to the actual situation, such as raw material availability, cost considerations, product purity requirements, etc.
To perform this nucleophilic substitution, suitable reaction conditions need to be selected. The choice of solvent is crucial. Polar aprotic solvents such as dimethyl sulfoxide (DMSO), N, N-dimethylformamide (DMF), etc. are often used. These solvents can improve the solubility and activity of nucleophiles without adverse effects on the reaction process.
The reaction temperature also needs to be fine-tuned. If it is too low, the reaction rate will be slow and take a long time; if it is too high, it may cause side reactions and lead to impure products. Generally speaking, moderate heating can speed up the reaction rate, but it needs to be controlled within a certain range, or between room temperature and moderate heating.
There is another method, which can first prepare an intermediate containing a hydrazine group, and then connect it with 1,3,5-trifluorobenzene through a specific reaction. The preparation of this intermediate can be achieved by means of functional group conversion and condensation according to the existing organic synthesis method. After the intermediate is ready, it is reacted with 1,3,5-trifluorobenzene under suitable conditions to obtain the target product 2-hydrazine-1,3,5-trifluorobenzene.
Furthermore, the catalytic reaction method may also be feasible. Selecting a suitable catalyst can promote the reaction, improve the selectivity and yield of the reaction. Some transition metal catalysts can effectively catalyze the reaction of hydrazine-containing reagents with 1,3,5-trifluorobenzene in specific organic reactions, making the reaction more efficient and specific. However, when using catalysts, it is necessary to consider their cost, activity and requirements for reaction conditions in order to achieve the best synthesis effect. All synthesis methods have advantages and disadvantages, and they need to be selected according to the actual situation, such as raw material availability, cost considerations, product purity requirements, etc.
What are the environmental effects of 2-bromo-1,3,5-trichlorobenzene?
2-% cyanogen-1,3,5-trifluorobenzene is also an organic compound. Its impact on the environment is worth exploring.
If this compound is released in the atmosphere, it is volatile or can be diffused in the air. However, its chemical properties are relatively stable and it is not easy to decompose rapidly, so it may remain in the atmosphere for a long time. And because of its fluorine, cyanide and other elements, or chemical reactions with other substances in the atmosphere, it interferes with the chemical composition of the atmosphere and may also affect the photochemical reaction process of the atmosphere. However, the specific degree of impact depends on its release and the specific circumstances of the surrounding atmospheric environment.
If it enters the water body, due to hydrophobicity, it may be adsorbed on suspended particles, and then settle to the bottom of the water, or form a film on the water surface, which affects the gas exchange between the water body and the atmosphere, causing damage to the living environment of aquatic organisms. The cyanide groups it contains are toxic, and may have toxic effects on aquatic organisms, such as fish and plankton, hindering their growth, reproduction, and even causing their death, thereby affecting the balance of the entire aquatic ecosystem.
In the soil environment, 2-% cyanogen-1,3,5-trifluorobenzene is chemically stable, and is not easily degraded by soil microorganisms, or will accumulate in the soil. In this way, it may affect the structure and function of microbial communities in the soil, change the physical and chemical properties of the soil, hinder the growth and development of plant roots, affect the absorption of nutrients by plants, and then affect the vegetation distribution and productivity of terrestrial ecosystems.
In summary, 2-% cyanogen-1,3,5-trifluorobenzene has many adverse effects on the environment, and its production, use and disposal should be treated with caution to reduce the harm caused to the environment.
If this compound is released in the atmosphere, it is volatile or can be diffused in the air. However, its chemical properties are relatively stable and it is not easy to decompose rapidly, so it may remain in the atmosphere for a long time. And because of its fluorine, cyanide and other elements, or chemical reactions with other substances in the atmosphere, it interferes with the chemical composition of the atmosphere and may also affect the photochemical reaction process of the atmosphere. However, the specific degree of impact depends on its release and the specific circumstances of the surrounding atmospheric environment.
If it enters the water body, due to hydrophobicity, it may be adsorbed on suspended particles, and then settle to the bottom of the water, or form a film on the water surface, which affects the gas exchange between the water body and the atmosphere, causing damage to the living environment of aquatic organisms. The cyanide groups it contains are toxic, and may have toxic effects on aquatic organisms, such as fish and plankton, hindering their growth, reproduction, and even causing their death, thereby affecting the balance of the entire aquatic ecosystem.
In the soil environment, 2-% cyanogen-1,3,5-trifluorobenzene is chemically stable, and is not easily degraded by soil microorganisms, or will accumulate in the soil. In this way, it may affect the structure and function of microbial communities in the soil, change the physical and chemical properties of the soil, hinder the growth and development of plant roots, affect the absorption of nutrients by plants, and then affect the vegetation distribution and productivity of terrestrial ecosystems.
In summary, 2-% cyanogen-1,3,5-trifluorobenzene has many adverse effects on the environment, and its production, use and disposal should be treated with caution to reduce the harm caused to the environment.
What should I pay attention to when storing and transporting 2-bromo-1,3,5-trichlorobenzene?
2-% cyanogen-1,3,5-trifluorobenzene is also a chemical substance. During storage and transportation, many matters need to be carefully paid attention to.
When storing, the first environment. It must be placed in a cool and ventilated warehouse, away from fires and heat sources. This is because the substance may be flammable or have dangerous reactions with heat and fire. The temperature of the warehouse should be strictly controlled, not too high, to prevent changes in the properties of the substance.
Furthermore, it should be stored separately from oxidants, acids, bases, etc., and must not be mixed. Because of its active chemical properties, contact with different types of chemical substances, or violent chemical reactions, resulting in safety accidents. Such as oxidizing agents, or oxidizing 2-% cyanogen-1,3,5-trifluorobenzene, causing combustion or even explosion.
Packaging is also critical. Packaging must be sealed to prevent moisture and leakage. If the package is damaged, the substance will come into contact with air, moisture, or deteriorate, and the leaked material or pollute the environment, endangering the safety of personnel.
When transporting, the transportation vehicle should be equipped with the corresponding variety and quantity of fire fighting equipment and leakage emergency treatment equipment. In this way, in case of emergencies, it can be responded quickly. During transportation, ensure that the container does not leak, collapse, fall, or damage. Driving routes should avoid densely populated areas, important facilities, etc., to prevent major casualties and losses from accidents. And transportation personnel must undergo professional training, be familiar with the characteristics of the substance and emergency treatment methods, operate strictly during transportation, and abide by relevant transportation regulations.
When storing, the first environment. It must be placed in a cool and ventilated warehouse, away from fires and heat sources. This is because the substance may be flammable or have dangerous reactions with heat and fire. The temperature of the warehouse should be strictly controlled, not too high, to prevent changes in the properties of the substance.
Furthermore, it should be stored separately from oxidants, acids, bases, etc., and must not be mixed. Because of its active chemical properties, contact with different types of chemical substances, or violent chemical reactions, resulting in safety accidents. Such as oxidizing agents, or oxidizing 2-% cyanogen-1,3,5-trifluorobenzene, causing combustion or even explosion.
Packaging is also critical. Packaging must be sealed to prevent moisture and leakage. If the package is damaged, the substance will come into contact with air, moisture, or deteriorate, and the leaked material or pollute the environment, endangering the safety of personnel.
When transporting, the transportation vehicle should be equipped with the corresponding variety and quantity of fire fighting equipment and leakage emergency treatment equipment. In this way, in case of emergencies, it can be responded quickly. During transportation, ensure that the container does not leak, collapse, fall, or damage. Driving routes should avoid densely populated areas, important facilities, etc., to prevent major casualties and losses from accidents. And transportation personnel must undergo professional training, be familiar with the characteristics of the substance and emergency treatment methods, operate strictly during transportation, and abide by relevant transportation regulations.
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