Linshang Chemical
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2,6-Dichloro-4-(Trifluoromethyloxy)Bromobenzene
Linshang Chemical
|
HS Code |
857852 |
| Chemical Formula | C7H3BrCl2F3O |
| Molecular Weight | 307.906 |
| Appearance | Typically a colorless to light - colored liquid or solid |
| Boiling Point | Data may vary, but around a certain temperature based on purity |
| Melting Point | Specific value depending on sample purity |
| Density | Certain value in g/cm³ at standard conditions |
| Solubility In Water | Low solubility, considered insoluble in water |
| Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, chloroform |
| Vapor Pressure | Low vapor pressure at room temperature |
| Flash Point | Determined by standard methods, a certain temperature value |
As an accredited 2,6-Dichloro-4-(Trifluoromethyloxy)Bromobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 2,6 - dichloro - 4-(trifluoromethyloxy)bromobenzene in a sealed glass bottle. |
| Storage | 2,6 - dichloro - 4-(trifluoromethyloxy)bromobenzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and oxidizing agents. Store in a tightly sealed container to prevent leakage and exposure to air and moisture, which could potentially cause degradation or chemical reactions. |
| Shipping | 2,6 - dichloro - 4-(trifluoromethyloxy)bromobenzene is shipped in specialized, tightly - sealed containers. It follows strict chemical transport regulations, ensuring safe transit due to its potentially hazardous nature. |
Competitive 2,6-Dichloro-4-(Trifluoromethyloxy)Bromobenzene 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 2,6-Dichloro-4-(Trifluoromethyloxy)Bromobenzene in China?
As a trusted 2,6-Dichloro-4-(Trifluoromethyloxy)Bromobenzene 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 2,6-Dichloro-4-(Trifluoromethyloxy)Bromobenzene 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 2,6-dichloro-4- (trifluoromethoxy) bromobenzene?
2% 2C6-difluoro-4- (triethoxyformyl) benzoic acid, which is widely used. In the field of medicinal chemistry, it is often used as a key intermediate to synthesize drugs with specific physiological activities. With its unique chemical structure, it can react ingeniously with other compounds to build complex drug molecular structures, making significant contributions to the development of drugs for the treatment of diseases such as cardiovascular diseases and tumors.
In the field of materials science, it can participate in the preparation of polymer materials. With its own characteristics, it endows materials with unique properties such as excellent thermal stability, chemical stability and optical properties. For example, high-performance engineering plastics are prepared for the manufacture of components in aerospace, electronic equipment, and other fields to meet the demanding performance requirements of materials in these fields.
In organic synthetic chemistry, it is an extremely important building block. Chemists can use various functional group conversion reactions to construct rich and diverse organic compounds, providing many possibilities for the development of organic synthetic chemistry and assisting scientists in exploring novel organic molecular structures and properties.
To sum up, 2% 2C6 -difluoro-4- (triethoxyformyl) benzoic acid plays a key role in many fields such as medicine, materials, and organic synthesis, and is of great significance for promoting technological progress and development in related fields.
In the field of materials science, it can participate in the preparation of polymer materials. With its own characteristics, it endows materials with unique properties such as excellent thermal stability, chemical stability and optical properties. For example, high-performance engineering plastics are prepared for the manufacture of components in aerospace, electronic equipment, and other fields to meet the demanding performance requirements of materials in these fields.
In organic synthetic chemistry, it is an extremely important building block. Chemists can use various functional group conversion reactions to construct rich and diverse organic compounds, providing many possibilities for the development of organic synthetic chemistry and assisting scientists in exploring novel organic molecular structures and properties.
To sum up, 2% 2C6 -difluoro-4- (triethoxyformyl) benzoic acid plays a key role in many fields such as medicine, materials, and organic synthesis, and is of great significance for promoting technological progress and development in related fields.
What are the synthesis methods of 2,6-dichloro-4- (trifluoromethoxy) bromobenzene?
To prepare 2,6-difluoro-4- (triethoxyformyl) quinoline, there are many methods.
First, start with the corresponding halogenated quinoline, and the reagent containing triethoxyformyl should be nucleophilic substitution. The halogen atom of the halogenated quinoline and the active group of the triethoxyformyl reagent should be substituted at a suitable temperature, pressure and catalyst existence. If the halogen of the halogenated quinoline is bromine, and the triethoxyformyl reagent is an active ester, under the catalysis of the base, the bromine atom can be replaced by the triethoxyformyl group to form the target product. Among them, the choice of base is very important, and its alkalinity, solubility and catalytic effect on the reaction need to be tested. Common examples are potassium carbonate, sodium carbonate, etc.
Second, quinoline derivatives are used as groups, and modified and converted by specific groups. First prepare quinoline containing modifiable groups, such as quinoline containing carboxyl groups, and then esterify it with ethanol and suitable catalysts and dehydrants to form ethoxyformyl groups. The process of esterification requires temperature control, time and material ratio to avoid side reactions. And the amount of ethanol and the activity of the catalyst are all related to the rate of the reaction and the purity of the product.
Third, adopt the strategy of cyclization reaction. The chain-like compound with suitable functional groups is used as the raw material, and under suitable reaction conditions, it is cyclized within the molecule to form a quinoline ring, and triethoxyformyl groups are introduced in this process. The structure of the raw material needs to be precisely set so that each functional group responds in sequence during the reaction to obtain the target cyclization product. For example, the carbon chain length of the raw material, the position and activity of the functional group, all need to be carefully considered to achieve the purpose of efficient cyclization and precise introduction of substituents.
All these methods have advantages and disadvantages, and the most suitable method should be selected according to the actual situation, such as the availability of raw materials, the level of cost, and the purity requirements of the product.
First, start with the corresponding halogenated quinoline, and the reagent containing triethoxyformyl should be nucleophilic substitution. The halogen atom of the halogenated quinoline and the active group of the triethoxyformyl reagent should be substituted at a suitable temperature, pressure and catalyst existence. If the halogen of the halogenated quinoline is bromine, and the triethoxyformyl reagent is an active ester, under the catalysis of the base, the bromine atom can be replaced by the triethoxyformyl group to form the target product. Among them, the choice of base is very important, and its alkalinity, solubility and catalytic effect on the reaction need to be tested. Common examples are potassium carbonate, sodium carbonate, etc.
Second, quinoline derivatives are used as groups, and modified and converted by specific groups. First prepare quinoline containing modifiable groups, such as quinoline containing carboxyl groups, and then esterify it with ethanol and suitable catalysts and dehydrants to form ethoxyformyl groups. The process of esterification requires temperature control, time and material ratio to avoid side reactions. And the amount of ethanol and the activity of the catalyst are all related to the rate of the reaction and the purity of the product.
Third, adopt the strategy of cyclization reaction. The chain-like compound with suitable functional groups is used as the raw material, and under suitable reaction conditions, it is cyclized within the molecule to form a quinoline ring, and triethoxyformyl groups are introduced in this process. The structure of the raw material needs to be precisely set so that each functional group responds in sequence during the reaction to obtain the target cyclization product. For example, the carbon chain length of the raw material, the position and activity of the functional group, all need to be carefully considered to achieve the purpose of efficient cyclization and precise introduction of substituents.
All these methods have advantages and disadvantages, and the most suitable method should be selected according to the actual situation, such as the availability of raw materials, the level of cost, and the purity requirements of the product.
What are the physical properties of 2,6-dichloro-4- (trifluoromethoxy) bromobenzene?
2% 2C6 -dideuterium-4- (triethoxyformyl) benzonitrile is a kind of organic compound. Its physical properties are quite specific.
Looking at its morphology, under normal temperature and pressure, it is mostly white to light yellow crystalline powder, like fine snow and clear particles. This morphology is conducive to storage and access, and is convenient for subsequent chemical reactions.
When it comes to melting point, it is about a specific temperature range. When the external temperature gradually rises to a certain value, the compound melts like ice in spring, slowly converting from solid to liquid. This temperature is its melting point. This property is crucial for the identification and purity judgment of the compound. The boiling point of
is also one of its important physical properties. In a specific pressure environment, when the temperature rises to the corresponding boiling point, the compound will turn from liquid to gaseous state and rise. The determination of boiling point can provide key parameters for its separation and purification.
In terms of solubility, it shows different solubility characteristics in common organic solvents. In some organic solvents, such as ethanol and acetone, it can be moderately dissolved, just like a salt melts in water to form a uniform solution; in water, its solubility is poor, mostly in suspension, and it is difficult to blend with water. This difference in solubility can be used in the extraction and separation of compounds.
Above the density, it also has its own unique value. Compared with water and other common liquids, it has a specific density relationship. This density characteristic needs to be taken into account when involving liquid-liquid separation, mixing and other operations.
In addition, it also has a certain stability, and can maintain its own chemical structure and properties under normal environmental conditions. When encountering extreme conditions such as high temperature, strong acid, and strong alkali, its structure may change, triggering chemical reactions. Therefore, when storing and using, it is necessary to choose a suitable environment.
Looking at its morphology, under normal temperature and pressure, it is mostly white to light yellow crystalline powder, like fine snow and clear particles. This morphology is conducive to storage and access, and is convenient for subsequent chemical reactions.
When it comes to melting point, it is about a specific temperature range. When the external temperature gradually rises to a certain value, the compound melts like ice in spring, slowly converting from solid to liquid. This temperature is its melting point. This property is crucial for the identification and purity judgment of the compound. The boiling point of
is also one of its important physical properties. In a specific pressure environment, when the temperature rises to the corresponding boiling point, the compound will turn from liquid to gaseous state and rise. The determination of boiling point can provide key parameters for its separation and purification.
In terms of solubility, it shows different solubility characteristics in common organic solvents. In some organic solvents, such as ethanol and acetone, it can be moderately dissolved, just like a salt melts in water to form a uniform solution; in water, its solubility is poor, mostly in suspension, and it is difficult to blend with water. This difference in solubility can be used in the extraction and separation of compounds.
Above the density, it also has its own unique value. Compared with water and other common liquids, it has a specific density relationship. This density characteristic needs to be taken into account when involving liquid-liquid separation, mixing and other operations.
In addition, it also has a certain stability, and can maintain its own chemical structure and properties under normal environmental conditions. When encountering extreme conditions such as high temperature, strong acid, and strong alkali, its structure may change, triggering chemical reactions. Therefore, when storing and using, it is necessary to choose a suitable environment.
What are the chemical properties of 2,6-dichloro-4- (trifluoromethoxy) bromobenzene
2% 2C6-difluoro-4- (triethoxyformyl) benzonitrile, which has many chemical properties. It contains fluorine atoms. Due to the strong electronegativity of fluorine atoms, the distribution of molecular electron clouds changes, resulting in its active chemical properties and easy to participate in nucleophilic substitution and other reactions.
From the perspective of nitrile groups, nitrile groups have high reactivity. Under appropriate conditions, carboxyl groups can be hydrolyzed to form carboxylic groups, or reacted with nucleophiles such as Grignard reagents to form new carbon-carbon bonds, which can be used in organic synthesis to expand carbon chains and introduce new functional groups.
Its benzene ring structure also affects chemical properties. The benzene ring has a conjugated system, which stabilizes the molecule. At the same time, it also provides a check point for the electrophilic substitution reaction. Because other functional groups are connected to the benzene ring, the localization effect selectively changes the electrophilic substitution reaction region.
In the triethoxy formyl group, the ethoxy group is the power supplier, which affects the electron cloud density distribution of the benzene ring, and the formyl group can undergo a variety of reactions, such as reduction to alcohol, condensation with compounds containing active hydrogen, etc.
In addition, due to the interaction of functional groups in the molecule, the overall chemical properties are complex. The synergistic action of different functional groups provides the possibility for diverse transformations in organic synthesis, which can be used to prepare compounds in the fields of drugs,
From the perspective of nitrile groups, nitrile groups have high reactivity. Under appropriate conditions, carboxyl groups can be hydrolyzed to form carboxylic groups, or reacted with nucleophiles such as Grignard reagents to form new carbon-carbon bonds, which can be used in organic synthesis to expand carbon chains and introduce new functional groups.
Its benzene ring structure also affects chemical properties. The benzene ring has a conjugated system, which stabilizes the molecule. At the same time, it also provides a check point for the electrophilic substitution reaction. Because other functional groups are connected to the benzene ring, the localization effect selectively changes the electrophilic substitution reaction region.
In the triethoxy formyl group, the ethoxy group is the power supplier, which affects the electron cloud density distribution of the benzene ring, and the formyl group can undergo a variety of reactions, such as reduction to alcohol, condensation with compounds containing active hydrogen, etc.
In addition, due to the interaction of functional groups in the molecule, the overall chemical properties are complex. The synergistic action of different functional groups provides the possibility for diverse transformations in organic synthesis, which can be used to prepare compounds in the fields of drugs,
What should be paid attention to when storing and transporting 2,6-dichloro-4- (trifluoromethoxy) bromobenzene?
2% 2C6-dioxy-4- (triethoxymethyl) benzofuran should be carefully stored and transported.
When hiding, it is the first environment. It should be placed in a cool and dry place away from direct sunlight. Sunlight is hot and can cause chemical changes, which can change the material properties and lose its original use. And in a cool and dry place, it can slow down its deterioration and ensure its quality. Furthermore, sealing is also necessary. This thing may be separated from moisture, oxygen, etc. in the air, and sealing can prevent its qualitative changes.
When shipping, the packaging must be firm. The road is bumpy. If the packaging is not solid, it is easy to cause the container to break and the material to leak out. Once it leaks, one is damaged, and the other may endanger the surroundings. And the person handling it should have professional knowledge and skills, know the nature of the material, understand its risks, and handle it with care when handling to avoid violent vibrations and collisions. And the means of transportation also need to be fit. If it is transported by car, the temperature and humidity in the car should be controllable to prevent high temperature and humidity from damaging its quality. And during transportation, the packaging should be checked frequently. If there is any damage, it should be dealt with quickly to avoid enlargement.
In short, regardless of the situation, it is necessary to maintain the stability and quantity of 2% 2C6 -dioxy-4- (triethoxy methyl) benzofuran, and it is not necessary to slack a little, causing accidents.
When hiding, it is the first environment. It should be placed in a cool and dry place away from direct sunlight. Sunlight is hot and can cause chemical changes, which can change the material properties and lose its original use. And in a cool and dry place, it can slow down its deterioration and ensure its quality. Furthermore, sealing is also necessary. This thing may be separated from moisture, oxygen, etc. in the air, and sealing can prevent its qualitative changes.
When shipping, the packaging must be firm. The road is bumpy. If the packaging is not solid, it is easy to cause the container to break and the material to leak out. Once it leaks, one is damaged, and the other may endanger the surroundings. And the person handling it should have professional knowledge and skills, know the nature of the material, understand its risks, and handle it with care when handling to avoid violent vibrations and collisions. And the means of transportation also need to be fit. If it is transported by car, the temperature and humidity in the car should be controllable to prevent high temperature and humidity from damaging its quality. And during transportation, the packaging should be checked frequently. If there is any damage, it should be dealt with quickly to avoid enlargement.
In short, regardless of the situation, it is necessary to maintain the stability and quantity of 2% 2C6 -dioxy-4- (triethoxy methyl) benzofuran, and it is not necessary to slack a little, causing accidents.
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