Linshang Chemical
PRODUCTS
1-Bromo-3-Chloro-2-(Trifluoromethyl)Benzene
Linshang Chemical
|
HS Code |
936453 |
| Chemical Formula | C7H3BrClF3 |
| Molecular Weight | 273.45 |
| Appearance | Liquid (Typical description for such compounds, exact needs verification) |
| Solubility In Water | Low (Aromatic halides are generally hydrophobic) |
| Solubility In Organic Solvents | Good in common organic solvents like dichloromethane, chloroform (Typical for aromatic halides) |
As an accredited 1-Bromo-3-Chloro-2-(Trifluoromethyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 1 - bromo - 3 - chloro - 2 - (trifluoromethyl)benzene packaged in a sealed glass bottle. |
| Storage | 1 - Bromo - 3 - chloro - 2 - (trifluoromethyl)benzene should be stored in a cool, dry, well - ventilated area away from heat sources and open flames. Keep it in a tightly closed container to prevent evaporation and exposure to air or moisture. Store it separately from oxidizing agents and reactive chemicals to avoid potential chemical reactions. |
| Shipping | 1 - bromo - 3 - chloro - 2 - (trifluoromethyl)benzene is a chemical. It should be shipped in tightly - sealed, corrosion - resistant containers, following all relevant hazardous materials regulations to ensure safe transportation. |
Competitive 1-Bromo-3-Chloro-2-(Trifluoromethyl)Benzene 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.
We will respond to you as soon as possible.
Tel: +8615365006308
Email: info@alchemist-chem.com
Where to Buy 1-Bromo-3-Chloro-2-(Trifluoromethyl)Benzene in China?
As a trusted 1-Bromo-3-Chloro-2-(Trifluoromethyl)Benzene 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 1-Bromo-3-Chloro-2-(Trifluoromethyl)Benzene 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 physical properties of 1-bromo-3-chloro-2 - (trifluoromethyl) benzene?
The physical properties of 1 + -ether-3-alkane-2- (triethylmethyl) naphthalene are as follows:
Viewed, this compound is mostly liquid at room temperature, and its color is almost colorless. When it is extremely pure, it may show a very light color, but it is also close to a colorless and transparent state. It is like water, but it has a unique quality. Its odor is specific, emitting a subtle and volatile smell. It smells it, or it feels fresh with a little special charm. However, this smell is not pungent and intolerable, but a milder volatile odor.
As for its boiling point, due to the characteristics of the molecular structure, it is about a certain temperature range under specific conditions. Due to the force between molecules, its boiling point is sufficient to maintain its liquid state at common ambient temperatures. Its melting point is also fixed. When it is relatively low temperature, the movement of molecules slows down and the attractive force between them increases, so it gradually turns from liquid to solid state. This melting point is a specific physical sign of the substance.
When it comes to density, it is slightly lighter than water. If it is co-placed with water in a container, it can be seen that it floats on the water surface. The boundaries are clear, and the two are incompatible with each other, just like Jingwei. This compound has good solubility in organic solvents and can be miscible with many organic solvents in a certain proportion. Because its molecular structure is similar to the principle of miscibility of organic solvents, it can be evenly dispersed in it.
Its conductivity is extremely weak and almost insulating. The cap has no free-moving charge carriers in its molecular structure, and it is difficult to form directional movement in it, whether it is ions or free electrons. It can be regarded as a good insulator in terms of electrical properties.
The above are all the physical properties of this 1 + -ether-3-alkane-2- (triethylmethyl) naphthalene.
Viewed, this compound is mostly liquid at room temperature, and its color is almost colorless. When it is extremely pure, it may show a very light color, but it is also close to a colorless and transparent state. It is like water, but it has a unique quality. Its odor is specific, emitting a subtle and volatile smell. It smells it, or it feels fresh with a little special charm. However, this smell is not pungent and intolerable, but a milder volatile odor.
As for its boiling point, due to the characteristics of the molecular structure, it is about a certain temperature range under specific conditions. Due to the force between molecules, its boiling point is sufficient to maintain its liquid state at common ambient temperatures. Its melting point is also fixed. When it is relatively low temperature, the movement of molecules slows down and the attractive force between them increases, so it gradually turns from liquid to solid state. This melting point is a specific physical sign of the substance.
When it comes to density, it is slightly lighter than water. If it is co-placed with water in a container, it can be seen that it floats on the water surface. The boundaries are clear, and the two are incompatible with each other, just like Jingwei. This compound has good solubility in organic solvents and can be miscible with many organic solvents in a certain proportion. Because its molecular structure is similar to the principle of miscibility of organic solvents, it can be evenly dispersed in it.
Its conductivity is extremely weak and almost insulating. The cap has no free-moving charge carriers in its molecular structure, and it is difficult to form directional movement in it, whether it is ions or free electrons. It can be regarded as a good insulator in terms of electrical properties.
The above are all the physical properties of this 1 + -ether-3-alkane-2- (triethylmethyl) naphthalene.
What are the chemical properties of 1-bromo-3-chloro-2- (trifluoromethyl) benzene?
The chemical properties of 1 + -alcohol-3-aldehyde-2- (triethylmethyl) benzene are as follows:
alcohol group, with active properties. First, it can cause a displacement reaction with sodium metal, such as ethanol in contact with sodium, to generate sodium ethanol and hydrogen. This is because hydrogen in the alcohol hydroxyl group has a certain activity, and sodium can replace it. Second, a elimination reaction can occur. When there is a suitable catalyst and conditions, the alcohol can remove a molecule of water to form an ethylene. Taking 1-alcohol as an example, under appropriate sulfuric acid catalysis and heating conditions, the hydrogen on the hydroxyl group and the adjacent carbon can be eliminated to form a carbon-carbon double bond. Third, esterification reaction can occur. Under the catalysis of concentrated sulfuric acid with carboxylic acid, the alcohol hydroxyl group dehydrates and condensates with the carboxyl group to form an ester and water. This reaction is reversible.
The aldehyde group is also an active functional group. It can be oxidized by weak oxidants such as silver ammonia solution to produce a silver mirror reaction to generate ammonium carboxylate, silver, ammonia gas and water, which is the embodiment of aldehyde group reduction; it can also be oxidized to carboxylic acid by strong oxidants such as acidic potassium permanganate solution. In addition, the aldehyde group can undergo an addition reaction with hydrogen. Under the action of the catalyst, the carbon-oxygen double bond in the aldehyde group is opened, and it is added with hydrogen to form an alcohol.
As for the triethyl group attached to the benzene ring, the benzene ring has special stability. However, the presence of triethyl methyl may affect the electron cloud density of the benzene ring, which in turn affects its substitution activity. In the electrophilic substitution reaction, triethyl methyl acts as the power supply group, which can increase the electron cloud density of the benzene ring at the o-para position, and is more prone to substitution reactions at the o-para position. When halogenation, nitrification, sulfonation and other reactions, the products are mostly o-para.
In summary, 1 + -ol-3-aldehyde-2- (triethyl) benzene contains alcohol groups, aldehyde groups and triethyl groups attached to the benzene ring structure, and has both alcohol, aldehyde and benzene ring-related chemical properties, showing unique behaviors in organic synthesis and reactions.
alcohol group, with active properties. First, it can cause a displacement reaction with sodium metal, such as ethanol in contact with sodium, to generate sodium ethanol and hydrogen. This is because hydrogen in the alcohol hydroxyl group has a certain activity, and sodium can replace it. Second, a elimination reaction can occur. When there is a suitable catalyst and conditions, the alcohol can remove a molecule of water to form an ethylene. Taking 1-alcohol as an example, under appropriate sulfuric acid catalysis and heating conditions, the hydrogen on the hydroxyl group and the adjacent carbon can be eliminated to form a carbon-carbon double bond. Third, esterification reaction can occur. Under the catalysis of concentrated sulfuric acid with carboxylic acid, the alcohol hydroxyl group dehydrates and condensates with the carboxyl group to form an ester and water. This reaction is reversible.
The aldehyde group is also an active functional group. It can be oxidized by weak oxidants such as silver ammonia solution to produce a silver mirror reaction to generate ammonium carboxylate, silver, ammonia gas and water, which is the embodiment of aldehyde group reduction; it can also be oxidized to carboxylic acid by strong oxidants such as acidic potassium permanganate solution. In addition, the aldehyde group can undergo an addition reaction with hydrogen. Under the action of the catalyst, the carbon-oxygen double bond in the aldehyde group is opened, and it is added with hydrogen to form an alcohol.
As for the triethyl group attached to the benzene ring, the benzene ring has special stability. However, the presence of triethyl methyl may affect the electron cloud density of the benzene ring, which in turn affects its substitution activity. In the electrophilic substitution reaction, triethyl methyl acts as the power supply group, which can increase the electron cloud density of the benzene ring at the o-para position, and is more prone to substitution reactions at the o-para position. When halogenation, nitrification, sulfonation and other reactions, the products are mostly o-para.
In summary, 1 + -ol-3-aldehyde-2- (triethyl) benzene contains alcohol groups, aldehyde groups and triethyl groups attached to the benzene ring structure, and has both alcohol, aldehyde and benzene ring-related chemical properties, showing unique behaviors in organic synthesis and reactions.
What are the main uses of 1-bromo-3-chloro-2 - (trifluoromethyl) benzene?
1 + -Mercury-3 + -arsenic-2- (triethyl) tin has a wide range of main uses. Mercury is involved in the refining of sand, the prescription of medicine, and the smelting of gold beads. The ancient alchemists often used mercury as a medicine, hoping for the pill of longevity. Although there are many falsehoods, it can also be seen that mercury is important in alchemy. In the medical way, there were also people who used mercury as medicine in the past, but now they know that it is poisonous and not dangerous, and it is rarely used. As for gold bead smelting, mercury can be used in gold panning and gold gilding, making the gold purer and the ornaments more beautiful.
Arsenic is useful in medicinal stones, insecticides, and dyeing. Ancient medicinal stone, arsenic agent is occasionally used as a medicine to treat scabies, sores and other diseases, but it is venomous and poisonous, so it must be used with caution. In the case of agricultural mulberry, arsenic can be used as an insecticide to ensure the safety of crops and prevent pests from disturbing. And in the dyeing and weaving industry, arsenic can help the color of pigments to be firm and bright, and make the color of fabrics beautiful and lasting.
2 - (triethyl) tin, often used as a chemical additive, is helpful in the polymerization reaction, the production of coatings, and the production of plastics. It can make the polymerization structure more stable, the coating performance is better, and the quality of plastics is better. However, it is also toxic, and it is potentially dangerous to the environment and the human body. Therefore, when using it, it is necessary to strictly abide by regulations to prevent its harm.
All these things, although each has its own use, are toxic. Those who use them should be clear about their advantages and disadvantages, and deal with them with scientific methods and caution. Only then can they obtain their advantages and avoid their harm, and maintain the safety of the people and the peace of the environment.
Arsenic is useful in medicinal stones, insecticides, and dyeing. Ancient medicinal stone, arsenic agent is occasionally used as a medicine to treat scabies, sores and other diseases, but it is venomous and poisonous, so it must be used with caution. In the case of agricultural mulberry, arsenic can be used as an insecticide to ensure the safety of crops and prevent pests from disturbing. And in the dyeing and weaving industry, arsenic can help the color of pigments to be firm and bright, and make the color of fabrics beautiful and lasting.
2 - (triethyl) tin, often used as a chemical additive, is helpful in the polymerization reaction, the production of coatings, and the production of plastics. It can make the polymerization structure more stable, the coating performance is better, and the quality of plastics is better. However, it is also toxic, and it is potentially dangerous to the environment and the human body. Therefore, when using it, it is necessary to strictly abide by regulations to prevent its harm.
All these things, although each has its own use, are toxic. Those who use them should be clear about their advantages and disadvantages, and deal with them with scientific methods and caution. Only then can they obtain their advantages and avoid their harm, and maintain the safety of the people and the peace of the environment.
What are the synthesis methods of 1-bromo-3-chloro-2 - (trifluoromethyl) benzene?
There are several methods for the synthesis of 1 + -ether-3-alkane-2- (triethylmethyl) benzene. The first method involves the interaction of halogenated alkanes with alkoxides. The halogen in the halogenated alkane is combined with the oxygen in the alcohol salt, and the other is synthesized into an ether. If the appropriate halogenated triethylmethane is mixed with the phenolic salt, put it in a suitable device, and add a moderate temperature to make the reaction take place. After time, this ether can be obtained.
The second method is to combine alcohol and alkene with the help of an acid catalyst. The double bond of the ethylene, when it encounters active hydrogen in the alcohol, breaks one of its bonds and forms a phase. When triethylenes and alcohols are co-placed in a device under the condition of the existence of an acid catalyst, the temperature and pressure are controlled, and the reaction process can also be formed into this 1 + -ether-3-alkane-2- (triethylmethyl) benzene.
There are also aryl halides and triethylboronic acid as raw materials. In the presence of appropriate metal catalysts, such as palladium catalysts, the two are combined with ligands to make a coupling reaction occur. In the reaction system, adjusting its pH, temperature and other conditions, the halogen atom interacts with the boric acid group, and the remainder is connected to obtain the target ether.
In addition, the method of oxide alkane and organometallic reagents can also be used. When the alkylene oxide encounters an organometallic reagent, its ring is broken, and the group of the reagent is connected. If an organometallic reagent containing triethyl methyl is reacted with an appropriate alkylene oxide, it can also be one of the ways to obtain this ether after subsequent treatment. All methods have advantages and disadvantages. According to the actual situation, such as the availability of raw materials, the cost, the difficulty of reaction, and the yield, etc., choose the appropriate one.
The second method is to combine alcohol and alkene with the help of an acid catalyst. The double bond of the ethylene, when it encounters active hydrogen in the alcohol, breaks one of its bonds and forms a phase. When triethylenes and alcohols are co-placed in a device under the condition of the existence of an acid catalyst, the temperature and pressure are controlled, and the reaction process can also be formed into this 1 + -ether-3-alkane-2- (triethylmethyl) benzene.
There are also aryl halides and triethylboronic acid as raw materials. In the presence of appropriate metal catalysts, such as palladium catalysts, the two are combined with ligands to make a coupling reaction occur. In the reaction system, adjusting its pH, temperature and other conditions, the halogen atom interacts with the boric acid group, and the remainder is connected to obtain the target ether.
In addition, the method of oxide alkane and organometallic reagents can also be used. When the alkylene oxide encounters an organometallic reagent, its ring is broken, and the group of the reagent is connected. If an organometallic reagent containing triethyl methyl is reacted with an appropriate alkylene oxide, it can also be one of the ways to obtain this ether after subsequent treatment. All methods have advantages and disadvantages. According to the actual situation, such as the availability of raw materials, the cost, the difficulty of reaction, and the yield, etc., choose the appropriate one.
What should I pay attention to when storing and transporting 1-bromo-3-chloro-2- (trifluoromethyl) benzene?
When storing and transporting benzene, many matters need careful attention.
Mercury is highly toxic, and its vapor inhaled into the human body can cause damage to the viscera and nerves. Therefore, when storing, be sure to store it in a closed container and choose a cool, dry and well-ventilated place to prevent the evaporation of mercury. When transporting, make sure that the container is leak-free and strictly protected so that mercury gas cannot escape, so as not to endanger the surrounding people.
Bromine is also highly corrosive and toxic, and has a severe irritation effect on the skin and mucous membranes. When storing, it should be stored separately from alkalis, active metal powders, etc., and must not be mixed. The container must be strong and well sealed to prevent the leakage of bromine liquid. During transportation, be careful to handle to avoid damage to the container caused by collision and the flow of bromine liquid.
As for triethylmethyl benzene, although the toxicity is relatively weak, it is a flammable organic compound. It is easy to burn and explode in case of open flames and hot topics. Storage should be in a cool and ventilated warehouse, away from fire and heat sources. The storage temperature should not exceed 30 ° C, and it should be stored separately from oxidizing agents. When transporting, the vehicles used should be equipped with fire protection and anti-static devices, and the densely populated areas and fire sources should be avoided during driving.
When the three coexist in one place, it is even more important to prevent possible chemical reactions between them. Be sure to follow relevant safety regulations and strict operation procedures, so as to ensure the safety of storage and transportation.
Mercury is highly toxic, and its vapor inhaled into the human body can cause damage to the viscera and nerves. Therefore, when storing, be sure to store it in a closed container and choose a cool, dry and well-ventilated place to prevent the evaporation of mercury. When transporting, make sure that the container is leak-free and strictly protected so that mercury gas cannot escape, so as not to endanger the surrounding people.
Bromine is also highly corrosive and toxic, and has a severe irritation effect on the skin and mucous membranes. When storing, it should be stored separately from alkalis, active metal powders, etc., and must not be mixed. The container must be strong and well sealed to prevent the leakage of bromine liquid. During transportation, be careful to handle to avoid damage to the container caused by collision and the flow of bromine liquid.
As for triethylmethyl benzene, although the toxicity is relatively weak, it is a flammable organic compound. It is easy to burn and explode in case of open flames and hot topics. Storage should be in a cool and ventilated warehouse, away from fire and heat sources. The storage temperature should not exceed 30 ° C, and it should be stored separately from oxidizing agents. When transporting, the vehicles used should be equipped with fire protection and anti-static devices, and the densely populated areas and fire sources should be avoided during driving.
When the three coexist in one place, it is even more important to prevent possible chemical reactions between them. Be sure to follow relevant safety regulations and strict operation procedures, so as to ensure the safety of storage and transportation.
Scan to WhatsApp
