Linshang Chemical
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2,4,6-Trichlorobenzeneboronic Acid
Linshang Chemical
|
HS Code |
980030 |
| Name | 2,4,6-Trichlorobenzeneboronic Acid |
| Chemical Formula | C6H3BCl3O2 |
| Molar Mass | 239.26 g/mol |
| Appearance | Solid |
| Physical State At Room Temp | Solid |
| Solubility In Water | Poorly soluble |
| Melting Point | 168 - 172 °C |
| Purity | Typically high purity for chemical use |
| Boiling Point | Decomposes before boiling |
| Odor | Odorless or very faint odor |
| Sensitivity | Moisture sensitive |
As an accredited 2,4,6-Trichlorobenzeneboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 2,4,6 - trichlorobenzeneboronic Acid in a sealed, chemical - resistant bottle. |
| Storage | 2,4,6 - Trichlorobenzeneboronic acid should be stored in a cool, dry place, away from heat sources and direct sunlight. Keep it in a well - sealed container to prevent moisture absorption and contact with air, which could lead to degradation. Store it separately from incompatible substances like strong oxidizing agents and bases to avoid chemical reactions. |
| Shipping | 2,4,6 - trichlorobenzeneboronic acid should be shipped in well - sealed, corrosion - resistant containers. Label containers clearly with hazard information. Ensure compliance with regulations for transporting chemicals to prevent spills and ensure safety during transit. |
Competitive 2,4,6-Trichlorobenzeneboronic Acid 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 2,4,6-Trichlorobenzeneboronic Acid in China?
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As a leading 2,4,6-Trichlorobenzeneboronic Acid 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 application fields of 2,4,6-trichlorophenylboronic acid
2% 2C4% 2C6-trifluorobenzoic acid is an important class of organic compounds. Its main application fields are widely used, as follows:
First, in the field of medicinal chemistry, this compound is a key intermediary. Due to its unique chemical properties, it can participate in the reaction pathways of many drug synthesis. For example, in the creation of some antibacterial and anti-inflammatory drugs, 2% 2C4% 2C6-trifluorobenzoic acid is often an indispensable raw material. Through ingenious organic synthesis methods and the incorporation of specific molecular structures, the drug is endowed with more outstanding biological activity and pharmacological properties, thereby enhancing the therapeutic effect of the drug on diseases.
Second, in the field of materials science, it also shows extraordinary value. In the preparation of high-performance polymer materials, 2% 2C4% 2C6-trifluorobenzoic acid can be used as a modifier. Its introduction can effectively improve the thermal stability, chemical stability and mechanical properties of polymers. For example, in the development of special polymer materials used in aerospace, adding an appropriate amount of this compound can make the material maintain excellent performance in extreme environments and ensure the safe and stable operation of all parts of the aircraft.
Third, in the field of pesticides, it also plays an important role. The synthesis of some new pesticides often relies on 2% 2C4% 2C6-trifluorobenzoic acid. The pesticides it participates in the synthesis have an efficient control effect on specific pests and weeds, and compared with traditional pesticides, it has lower toxicity and better environmental compatibility, which is in line with the current green agricultural development concept and helps to achieve sustainable development of agriculture.
In summary, 2% 2C4% 2C6-trifluorobenzoic acid has key applications in many fields such as medicine, materials, and pesticides, and has made great contributions to the development of related industries.
First, in the field of medicinal chemistry, this compound is a key intermediary. Due to its unique chemical properties, it can participate in the reaction pathways of many drug synthesis. For example, in the creation of some antibacterial and anti-inflammatory drugs, 2% 2C4% 2C6-trifluorobenzoic acid is often an indispensable raw material. Through ingenious organic synthesis methods and the incorporation of specific molecular structures, the drug is endowed with more outstanding biological activity and pharmacological properties, thereby enhancing the therapeutic effect of the drug on diseases.
Second, in the field of materials science, it also shows extraordinary value. In the preparation of high-performance polymer materials, 2% 2C4% 2C6-trifluorobenzoic acid can be used as a modifier. Its introduction can effectively improve the thermal stability, chemical stability and mechanical properties of polymers. For example, in the development of special polymer materials used in aerospace, adding an appropriate amount of this compound can make the material maintain excellent performance in extreme environments and ensure the safe and stable operation of all parts of the aircraft.
Third, in the field of pesticides, it also plays an important role. The synthesis of some new pesticides often relies on 2% 2C4% 2C6-trifluorobenzoic acid. The pesticides it participates in the synthesis have an efficient control effect on specific pests and weeds, and compared with traditional pesticides, it has lower toxicity and better environmental compatibility, which is in line with the current green agricultural development concept and helps to achieve sustainable development of agriculture.
In summary, 2% 2C4% 2C6-trifluorobenzoic acid has key applications in many fields such as medicine, materials, and pesticides, and has made great contributions to the development of related industries.
What is the synthesis method of 2,4,6-trichlorophenylboronic acid?
The synthesis of 2% 2C4% 2C6-trifluorobenzoacetic acid is a key issue in the field of organic synthesis. To make this compound, several ways can be followed, the following are the details:
The first method to use benzoacetic acid as the starting material is to introduce the method of using benzoacetic acid as the starting material. Co-preparing benzoacetic acid with fluorine-containing reagents such as trifluoroacetic anhydride or trifluoromethanesulfonic anhydride under suitable reaction conditions. During the reaction, a specific catalyst may be required to promote its efficient conversion. This catalyst may be some metal salts, such as zinc salts, aluminum salts, etc., by means of its catalytic activity, the reaction process is accelerated, and the specific position of benzoyl acetic acid is substituted with fluorine-containing reagents to gradually generate the target product 2% 2C4% 2C6-trifluorobenzoyl acetic acid. The temperature and reaction time of the reaction environment are key factors and need to be carefully regulated. Generally speaking, the temperature may be maintained in a moderate range, such as 40 to 80 degrees Celsius, and the reaction takes several hours to more than ten hours, depending on the specific reaction conditions.
Another method is to use benzene derivatives as starting materials. First, the benzene derivative is introduced into functional groups such as acyl and carboxyl groups through specific reaction steps to construct a structure similar to benzoyl acetic acid. Subsequently, a fluorine-containing reagent is applied to the resulting intermediate to achieve the introduction of fluorine atoms. In this process, the order of introducing functional groups and the precise control of reaction conditions are crucial. For example, when introducing acyl groups, a suitable acylating reagent, such as acid chloride or anhydride, may be selected, and the reaction is carried out in the presence of a suitable base to ensure that the acyl groups are accurately connected to the specific position of the benzene ring. After the key intermediates are generated, they are reacted with fluorine-containing reagents. By optimizing the reaction parameters, such as the choice of reaction solvent, the adjustment of reaction temperature and time, the fluorine atoms are smoothly integrated, and the final result is 2% 2C4% 2C6-trifluorobenzoylacetic acid.
Furthermore, there are also strategies for gradually constructing target molecules through multi-step reactions using other related compounds as starting materials. This approach may involve more complex reaction sequences, including the formation of carbon-carbon bonds, the transformation and modification of functional groups, and many other steps. Each step requires strict control of conditions to ensure the selectivity and yield of the reaction. If organometallic reagents are used to participate in the reaction, precise carbon-carbon bond coupling can be achieved, laying the foundation for the construction of the target molecule. Subsequently, through the rational transformation of functional groups and the introduction of fluorine atoms, the molecular structure is carefully crafted, and the purpose of synthesizing 2% 2C4% 2C6-trifluorobenzoyl acetic acid is finally achieved.
The first method to use benzoacetic acid as the starting material is to introduce the method of using benzoacetic acid as the starting material. Co-preparing benzoacetic acid with fluorine-containing reagents such as trifluoroacetic anhydride or trifluoromethanesulfonic anhydride under suitable reaction conditions. During the reaction, a specific catalyst may be required to promote its efficient conversion. This catalyst may be some metal salts, such as zinc salts, aluminum salts, etc., by means of its catalytic activity, the reaction process is accelerated, and the specific position of benzoyl acetic acid is substituted with fluorine-containing reagents to gradually generate the target product 2% 2C4% 2C6-trifluorobenzoyl acetic acid. The temperature and reaction time of the reaction environment are key factors and need to be carefully regulated. Generally speaking, the temperature may be maintained in a moderate range, such as 40 to 80 degrees Celsius, and the reaction takes several hours to more than ten hours, depending on the specific reaction conditions.
Another method is to use benzene derivatives as starting materials. First, the benzene derivative is introduced into functional groups such as acyl and carboxyl groups through specific reaction steps to construct a structure similar to benzoyl acetic acid. Subsequently, a fluorine-containing reagent is applied to the resulting intermediate to achieve the introduction of fluorine atoms. In this process, the order of introducing functional groups and the precise control of reaction conditions are crucial. For example, when introducing acyl groups, a suitable acylating reagent, such as acid chloride or anhydride, may be selected, and the reaction is carried out in the presence of a suitable base to ensure that the acyl groups are accurately connected to the specific position of the benzene ring. After the key intermediates are generated, they are reacted with fluorine-containing reagents. By optimizing the reaction parameters, such as the choice of reaction solvent, the adjustment of reaction temperature and time, the fluorine atoms are smoothly integrated, and the final result is 2% 2C4% 2C6-trifluorobenzoylacetic acid.
Furthermore, there are also strategies for gradually constructing target molecules through multi-step reactions using other related compounds as starting materials. This approach may involve more complex reaction sequences, including the formation of carbon-carbon bonds, the transformation and modification of functional groups, and many other steps. Each step requires strict control of conditions to ensure the selectivity and yield of the reaction. If organometallic reagents are used to participate in the reaction, precise carbon-carbon bond coupling can be achieved, laying the foundation for the construction of the target molecule. Subsequently, through the rational transformation of functional groups and the introduction of fluorine atoms, the molecular structure is carefully crafted, and the purpose of synthesizing 2% 2C4% 2C6-trifluorobenzoyl acetic acid is finally achieved.
What are the physical and chemical properties of 2,4,6-trichlorophenylboronic acid?
2% 2C4% 2C6-tribromobenzoic acid, its physical and chemical properties are as follows:
This substance is white to light yellow powder, with a slightly special odor. The melting point is quite high, about 250-254 ° C, at which temperature it melts from solid to liquid. Its boiling point is also high, and the specific value will vary depending on the measurement conditions, but it is generally in a decomposition rather than a boiling state, because it is easy to decompose at high temperatures.
In terms of solubility, 2% 2C4% 2C6-tribromobenzoic acid is slightly soluble in water, because the ratio of polar groups to non-polar groups in its molecular structure makes it difficult for water molecules to disperse it effectively. However, it can be soluble in organic solvents such as ethanol, ether, chloroform, etc. In organic solvents, a suitable interaction force can be formed between solute molecules and solvent molecules, so that it can be dissolved.
Chemically, it is acidic, and the carboxyl group on the benzene ring can ionize hydrogen ions, which can neutralize with bases to generate corresponding carboxylic salts and water. And because of the presence of bromine atoms on the benzene ring, it can participate in nucleophilic substitution reactions. The electronegativity of bromine atoms affects the electron cloud density distribution of the benzene ring, causing it to be replaced by other nucleophilic reagents under certain conditions, and then a variety of organic compounds can be derived. Due to the particularity of its structure, under the action of light or specific catalysts, some unique photochemical reactions or catalytic reactions can also occur, which has certain application value in the field of organic synthesis.
This substance is white to light yellow powder, with a slightly special odor. The melting point is quite high, about 250-254 ° C, at which temperature it melts from solid to liquid. Its boiling point is also high, and the specific value will vary depending on the measurement conditions, but it is generally in a decomposition rather than a boiling state, because it is easy to decompose at high temperatures.
In terms of solubility, 2% 2C4% 2C6-tribromobenzoic acid is slightly soluble in water, because the ratio of polar groups to non-polar groups in its molecular structure makes it difficult for water molecules to disperse it effectively. However, it can be soluble in organic solvents such as ethanol, ether, chloroform, etc. In organic solvents, a suitable interaction force can be formed between solute molecules and solvent molecules, so that it can be dissolved.
Chemically, it is acidic, and the carboxyl group on the benzene ring can ionize hydrogen ions, which can neutralize with bases to generate corresponding carboxylic salts and water. And because of the presence of bromine atoms on the benzene ring, it can participate in nucleophilic substitution reactions. The electronegativity of bromine atoms affects the electron cloud density distribution of the benzene ring, causing it to be replaced by other nucleophilic reagents under certain conditions, and then a variety of organic compounds can be derived. Due to the particularity of its structure, under the action of light or specific catalysts, some unique photochemical reactions or catalytic reactions can also occur, which has certain application value in the field of organic synthesis.
What is the price range of 2,4,6-trichlorophenylboronic acid in the market?
In today's market, the price of 2,4,6-trifluorobenzoic acid often varies due to factors such as quality, supply and demand. Generally speaking, its price per kilogram may range from a few hundred to several thousand yuan. If the quality is high, and there is a large number of people in the market who need it, but there are few people who supply it, the price may increase, reaching several thousand yuan per kilogram. However, if the quality is average and the supply exceeds the demand, the price may drop to several hundred yuan per kilogram.
The price is also different from merchant to merchant. There are those who use small profits but quick turnover as a strategy, and the price may be slightly lower; there are those who focus on quality and goodwill, and the price may be slightly higher. And the price of different regions also varies due to transportation, taxes, etc. In the capital of Dayi, merchants converge, the competition is fierce, and the price may be relatively easy; in remote places, due to the difficulty of transportation and the increase in cost, the price may be slightly higher.
Therefore, if you want to know the exact price, you should carefully observe the market conditions and visit merchants to compare their quality and price. And the market conditions are changing rapidly, and the price also changes from time to time, so you can't stick to the price of a moment.
The price is also different from merchant to merchant. There are those who use small profits but quick turnover as a strategy, and the price may be slightly lower; there are those who focus on quality and goodwill, and the price may be slightly higher. And the price of different regions also varies due to transportation, taxes, etc. In the capital of Dayi, merchants converge, the competition is fierce, and the price may be relatively easy; in remote places, due to the difficulty of transportation and the increase in cost, the price may be slightly higher.
Therefore, if you want to know the exact price, you should carefully observe the market conditions and visit merchants to compare their quality and price. And the market conditions are changing rapidly, and the price also changes from time to time, so you can't stick to the price of a moment.
What are the storage conditions for 2,4,6-trichlorophenylboronic acid?
2% 2C4% 2C6-trifluorobenzoic acid is also an organic compound. Its storage conditions are quite important, which is related to the stability and quality of this substance.
In the context of "Tiangong Kaiwu", although such chemicals were not common at that time, they can be stored today according to ancient principles. If you want to store 2% 2C4% 2C6-trifluorobenzoic acid well, you should first keep it in a cool place away from light. Exposure to sunlight may cause its structure to change and its chemical properties to change. Therefore, it is appropriate to hide in a dark room, and the room temperature should not be too high. It is better to use a cool place. If the cover temperature is too high, it is easy to promote its reaction and damage its quality.
Second, it is moisture-proof. Moisture is the enemy of many substances, and 2% 2C4% 2C6-trifluorobenzoic acid is no exception. Moisture invades, or causes reactions such as hydrolysis, which will damage its purity and effectiveness. Therefore, it should be stored in a sealed container, and a desiccant can be placed in the container to eliminate the danger of moisture.
Furthermore, the storage place must be kept away from fire sources and oxidants. If this compound encounters an open flame or a strong oxidant, it may react violently and cause the risk of explosion. A safe place must be selected, and flammable, explosive and strong oxidizing substances should not be placed around.
Also, the storage place should be well ventilated. If the ventilation is not smooth, the volatile gas of the compound will accumulate and not disperse, which is harmful to human health on the one hand, and may cause the gas concentration to reach a dangerous environment. In case of open flames, it is necessary to circulate the air to ensure the safety of the environment.
All these are the important principles for the storage of 2% 2C4% 2C6-trifluorobenzoic acid. According to this, the material can be stable for a long time for later use.
In the context of "Tiangong Kaiwu", although such chemicals were not common at that time, they can be stored today according to ancient principles. If you want to store 2% 2C4% 2C6-trifluorobenzoic acid well, you should first keep it in a cool place away from light. Exposure to sunlight may cause its structure to change and its chemical properties to change. Therefore, it is appropriate to hide in a dark room, and the room temperature should not be too high. It is better to use a cool place. If the cover temperature is too high, it is easy to promote its reaction and damage its quality.
Second, it is moisture-proof. Moisture is the enemy of many substances, and 2% 2C4% 2C6-trifluorobenzoic acid is no exception. Moisture invades, or causes reactions such as hydrolysis, which will damage its purity and effectiveness. Therefore, it should be stored in a sealed container, and a desiccant can be placed in the container to eliminate the danger of moisture.
Furthermore, the storage place must be kept away from fire sources and oxidants. If this compound encounters an open flame or a strong oxidant, it may react violently and cause the risk of explosion. A safe place must be selected, and flammable, explosive and strong oxidizing substances should not be placed around.
Also, the storage place should be well ventilated. If the ventilation is not smooth, the volatile gas of the compound will accumulate and not disperse, which is harmful to human health on the one hand, and may cause the gas concentration to reach a dangerous environment. In case of open flames, it is necessary to circulate the air to ensure the safety of the environment.
All these are the important principles for the storage of 2% 2C4% 2C6-trifluorobenzoic acid. According to this, the material can be stable for a long time for later use.
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