Linshang Chemical
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1-Chloro-3-(Trifluoromethyl)Benzene
Linshang Chemical
|
HS Code |
663697 |
| Chemical Formula | C7H4ClF3 |
| Molar Mass | 180.554 g/mol |
| Appearance | Colorless liquid |
| Boiling Point | 136 - 137 °C |
| Melting Point | −46 °C |
| Density | 1.328 g/mL at 25 °C |
| Vapor Pressure | ~2.5 kPa at 25 °C |
| Flash Point | 37 °C |
| Solubility In Water | Insoluble |
| Logp | 3.71 |
| Refractive Index | 1.445 - 1.447 |
As an accredited 1-Chloro-3-(Trifluoromethyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1 - chloro - 3 - (trifluoromethyl)benzene: 500 mL in a sealed, labeled glass bottle. |
| Storage | 1 - Chloro - 3 - (trifluoromethyl)benzene should be stored in a cool, well - ventilated area, away from heat sources and ignition points. It is a flammable liquid, so keep it separate from oxidizing agents. Store it in tightly - sealed containers made of materials resistant to corrosion, like stainless steel or certain plastics, to prevent leakage and ensure safety. |
| Shipping | 1 - Chloro - 3 - (trifluoromethyl)benzene is shipped in tightly sealed, corrosion - resistant containers. Transport follows strict chemical safety regulations, ensuring protection from environmental factors and potential spills during transit. |
Competitive 1-Chloro-3-(Trifluoromethyl)Benzene prices that fit your budget—flexible terms and customized quotes for every order.
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Tel: +8615365006308
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As a leading 1-Chloro-3-(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 main uses of 1-chloro-3- (trifluoromethyl) benzene?
1 + -Deuterium-3- (triethylmethyl) benzene is a commonly used organic compound in industry, and its main uses are quite extensive.
In the field of organic synthesis, this compound is often used as a key intermediate. Take the preparation of aromatic compounds with specific structures as an example. Its unique chemical structure can be skillfully combined with other reagents through many chemical reactions, such as nucleophilic substitution, electrophilic substitution, etc., to gradually construct complex and functional organic molecules. In the fine chemical industry, the synthesis of many high-value-added products relies on it as a starting material or an important intermediate. After a series of carefully designed reaction steps, various fine chemicals with excellent properties can be derived.
In the field of materials science, 1 + -deuterium-3- (triethylmethyl) benzene also shows unique value. In the preparation of some high-performance polymer materials, the introduction of this compound can effectively adjust the physical and chemical properties of the material. By ingeniously integrating it into the main chain or side chain of the polymer, the thermal stability, mechanical properties, solubility, etc. of the material can be improved. In the field of electronic materials, based on its special electron cloud distribution and structural characteristics, it can be used to prepare materials with specific electrical properties, providing the possibility for performance optimization and innovation of electronic components.
In addition, in the field of medicinal chemistry, it also plays an important role in the synthesis of drugs. With its participation in a specific reaction route, it may be possible to build a molecular skeleton closely related to drug activity. In some drug development processes, structural modification and derivatization based on 1 + -deuterium-3- (triethylmethyl) benzene is expected to obtain new drug molecules with better pharmacological activity and lower toxic and side effects.
In the field of organic synthesis, this compound is often used as a key intermediate. Take the preparation of aromatic compounds with specific structures as an example. Its unique chemical structure can be skillfully combined with other reagents through many chemical reactions, such as nucleophilic substitution, electrophilic substitution, etc., to gradually construct complex and functional organic molecules. In the fine chemical industry, the synthesis of many high-value-added products relies on it as a starting material or an important intermediate. After a series of carefully designed reaction steps, various fine chemicals with excellent properties can be derived.
In the field of materials science, 1 + -deuterium-3- (triethylmethyl) benzene also shows unique value. In the preparation of some high-performance polymer materials, the introduction of this compound can effectively adjust the physical and chemical properties of the material. By ingeniously integrating it into the main chain or side chain of the polymer, the thermal stability, mechanical properties, solubility, etc. of the material can be improved. In the field of electronic materials, based on its special electron cloud distribution and structural characteristics, it can be used to prepare materials with specific electrical properties, providing the possibility for performance optimization and innovation of electronic components.
In addition, in the field of medicinal chemistry, it also plays an important role in the synthesis of drugs. With its participation in a specific reaction route, it may be possible to build a molecular skeleton closely related to drug activity. In some drug development processes, structural modification and derivatization based on 1 + -deuterium-3- (triethylmethyl) benzene is expected to obtain new drug molecules with better pharmacological activity and lower toxic and side effects.
What are the physical properties of 1-chloro-3- (trifluoromethyl) benzene?
1 + -Neon-3- (triethylmethyl) benzene is one of the organic compounds. Its physical properties are quite important, and they are described in ancient Chinese.
First of all, under room temperature, 1 + -neon-3- (triethylmethyl) benzene is mostly in a colorless and transparent liquid state, like clear water, with a pure texture and no impurities. Its color is clear and translucent, and it looks like a clear spring without the slightest chaotic color.
Second and smell, this thing emits a special fragrance, which is rich in aroma but not pungent, but it cannot be smelled for a long time to prevent damage to the body. This fragrance is different from the ordinary floral and fruity fragrance, and has its own characteristics. It is one of the symbols in the category of organic compounds.
Furthermore, on its boiling point and melting point. The number of boiling points, according to experiments, can reach a certain temperature under specific conditions. At this temperature, the substance gradually changes from liquid to gaseous and becomes invisible. The melting point is also fixed. When the temperature drops to a certain value, 1 + -neon-3- (triethylmethyl) benzene will condense from liquid to solid, and the texture will become hard, like ice crystals, but its structure is very different from that of ice crystals.
As for the density, it is slightly lighter than water, so if it is mixed with water, it can be seen that it floats on the water surface, the boundaries are clear, and it does not blend with water, and the two are in their respective positions.
Solubility is also an important physical property. 1 + -neon-3- (triethylmethyl) benzene is soluble and homogeneous in organic solvents, such as ethanol, ether, etc., just like the state of water emulsion. However, in water, it is insoluble, and the two repel each other and form separate systems. This is due to the difference between its molecular structure and water.
In addition, 1 + -neon-3- (triethylmethyl) benzene is volatile to a certain extent. When placed in the air, its molecules gradually dissipate, changing from liquid to gaseous and mixed into the air. Therefore, when stored, it needs to be properly sealed to prevent it from evaporating.
First of all, under room temperature, 1 + -neon-3- (triethylmethyl) benzene is mostly in a colorless and transparent liquid state, like clear water, with a pure texture and no impurities. Its color is clear and translucent, and it looks like a clear spring without the slightest chaotic color.
Second and smell, this thing emits a special fragrance, which is rich in aroma but not pungent, but it cannot be smelled for a long time to prevent damage to the body. This fragrance is different from the ordinary floral and fruity fragrance, and has its own characteristics. It is one of the symbols in the category of organic compounds.
Furthermore, on its boiling point and melting point. The number of boiling points, according to experiments, can reach a certain temperature under specific conditions. At this temperature, the substance gradually changes from liquid to gaseous and becomes invisible. The melting point is also fixed. When the temperature drops to a certain value, 1 + -neon-3- (triethylmethyl) benzene will condense from liquid to solid, and the texture will become hard, like ice crystals, but its structure is very different from that of ice crystals.
As for the density, it is slightly lighter than water, so if it is mixed with water, it can be seen that it floats on the water surface, the boundaries are clear, and it does not blend with water, and the two are in their respective positions.
Solubility is also an important physical property. 1 + -neon-3- (triethylmethyl) benzene is soluble and homogeneous in organic solvents, such as ethanol, ether, etc., just like the state of water emulsion. However, in water, it is insoluble, and the two repel each other and form separate systems. This is due to the difference between its molecular structure and water.
In addition, 1 + -neon-3- (triethylmethyl) benzene is volatile to a certain extent. When placed in the air, its molecules gradually dissipate, changing from liquid to gaseous and mixed into the air. Therefore, when stored, it needs to be properly sealed to prevent it from evaporating.
What are the chemical properties of 1-chloro-3- (trifluoromethyl) benzene?
1 + -Alkane-3- (triethylmethyl) benzene is one of the organic compounds. Its chemical properties are of great value to explore.
In terms of physical properties, such compounds are usually liquid and have a special odor. Its boiling point, melting point and other properties are affected by the interaction between alkyl groups and benzene rings in the molecular structure. The presence of benzene rings gives it certain stability, and the structural differences of alkyl groups make the boiling point and melting point change.
As for chemical properties, first, this compound is aromatic. The conjugated π electronic system of benzene rings makes it prone to electrophilic substitution reactions. Electrophilic substitution reactions such as halogenation, nitration, and sulfonation can be carried out under appropriate conditions. Due to the distribution of electron cloud density on the benzene ring, electrophilic reagents tend to attack specific positions. Taking the halogenation reaction as an example, under the catalysis of Lewis acid, halogens can replace the hydrogen atoms on the benzene ring to form halogenated derivatives.
Second, the alkyl group of the side chain is also reactive. Under the influence of the benzene ring, the α-hydrogen atom is more active and can undergo oxidation reaction. Under the action of a suitable oxidant, α-carbon can be oxidized to form corresponding alcohol, aldehyde or carboxylic acid compounds. If the side chain is long, under certain conditions, a radical substitution reaction can also occur, and the hydrogen atom on the alkyl group is replaced by other groups.
Third, the compound can form complexes with certain metal ions or compounds. The electron cloud on the benzene ring and alkyl group can interact with metal ions to form complexes with specific structures and properties, which may have potential applications in catalysis, materials science and other fields.
Overall, 1 + -alkane-3- (triethylmethyl) benzene has broad application prospects in many fields such as organic synthesis, medicinal chemistry and materials science due to its unique molecular structure and the chemical properties of both benzene ring and alkyl group. It is an interesting object in chemical research.
In terms of physical properties, such compounds are usually liquid and have a special odor. Its boiling point, melting point and other properties are affected by the interaction between alkyl groups and benzene rings in the molecular structure. The presence of benzene rings gives it certain stability, and the structural differences of alkyl groups make the boiling point and melting point change.
As for chemical properties, first, this compound is aromatic. The conjugated π electronic system of benzene rings makes it prone to electrophilic substitution reactions. Electrophilic substitution reactions such as halogenation, nitration, and sulfonation can be carried out under appropriate conditions. Due to the distribution of electron cloud density on the benzene ring, electrophilic reagents tend to attack specific positions. Taking the halogenation reaction as an example, under the catalysis of Lewis acid, halogens can replace the hydrogen atoms on the benzene ring to form halogenated derivatives.
Second, the alkyl group of the side chain is also reactive. Under the influence of the benzene ring, the α-hydrogen atom is more active and can undergo oxidation reaction. Under the action of a suitable oxidant, α-carbon can be oxidized to form corresponding alcohol, aldehyde or carboxylic acid compounds. If the side chain is long, under certain conditions, a radical substitution reaction can also occur, and the hydrogen atom on the alkyl group is replaced by other groups.
Third, the compound can form complexes with certain metal ions or compounds. The electron cloud on the benzene ring and alkyl group can interact with metal ions to form complexes with specific structures and properties, which may have potential applications in catalysis, materials science and other fields.
Overall, 1 + -alkane-3- (triethylmethyl) benzene has broad application prospects in many fields such as organic synthesis, medicinal chemistry and materials science due to its unique molecular structure and the chemical properties of both benzene ring and alkyl group. It is an interesting object in chemical research.
What is the production method of 1-chloro-3- (trifluoromethyl) benzene?
To prepare 1-bromo-3- (triethyl) benzene, the following method can be used.
First take an appropriate amount of 3- (triethyl) benzene and place it in a clean and dry reaction vessel. This vessel needs to have good sealing and suitable reaction conditions.
Prepare a brominating reagent, usually liquid bromine. In order to make the reaction proceed smoothly and avoid excessive side reactions, an appropriate amount of catalyst can be added. For example, iron powder or iron tribromide is used as a catalyst. When the catalyst is slowly added to the reaction vessel containing 3- (triethyl) benzene, close attention should be paid to the changes in the reaction system.
When adding liquid bromine, it is advisable to add it dropwise slowly. Because the reaction is an exothermic reaction, if liquid bromine is added too fast, the reaction is too violent, and it is easy to cause temperature runaway, thereby triggering many unnecessary side reactions. During the dropwise addition process, a cooling device can be used to maintain the reaction temperature within an appropriate range.
During the reaction process, continuously stir the reaction mixture to ensure that the reactants can be fully contacted, speed up the reaction rate, and improve the reaction efficiency.
After the reaction is completed, the product needs to be separated and purified. First extract with a suitable organic solvent to separate the organic phase. Then distillation and other means are used to remove unreacted raw materials and by-products according to the difference in boiling points of each component, so as to obtain pure 1-bromo-3- (triethyl) benzene.
During the whole process, it is crucial to control the reaction conditions. Factors such as temperature, catalyst dosage, and reactant ratio will have a significant impact on the reaction results. Fine operation is required to achieve the desired preparation effect.
First take an appropriate amount of 3- (triethyl) benzene and place it in a clean and dry reaction vessel. This vessel needs to have good sealing and suitable reaction conditions.
Prepare a brominating reagent, usually liquid bromine. In order to make the reaction proceed smoothly and avoid excessive side reactions, an appropriate amount of catalyst can be added. For example, iron powder or iron tribromide is used as a catalyst. When the catalyst is slowly added to the reaction vessel containing 3- (triethyl) benzene, close attention should be paid to the changes in the reaction system.
When adding liquid bromine, it is advisable to add it dropwise slowly. Because the reaction is an exothermic reaction, if liquid bromine is added too fast, the reaction is too violent, and it is easy to cause temperature runaway, thereby triggering many unnecessary side reactions. During the dropwise addition process, a cooling device can be used to maintain the reaction temperature within an appropriate range.
During the reaction process, continuously stir the reaction mixture to ensure that the reactants can be fully contacted, speed up the reaction rate, and improve the reaction efficiency.
After the reaction is completed, the product needs to be separated and purified. First extract with a suitable organic solvent to separate the organic phase. Then distillation and other means are used to remove unreacted raw materials and by-products according to the difference in boiling points of each component, so as to obtain pure 1-bromo-3- (triethyl) benzene.
During the whole process, it is crucial to control the reaction conditions. Factors such as temperature, catalyst dosage, and reactant ratio will have a significant impact on the reaction results. Fine operation is required to achieve the desired preparation effect.
What are the precautions for using 1-chloro-3- (trifluoromethyl) benzene?
During the use of 1 + -bromo-3- (triethylmethyl) benzene, many things need to be paid attention to.
First, it is related to its chemical properties. This compound has certain reactivity, and when it encounters strong oxidants, strong acids and other substances, it is easy to cause violent chemical reactions, or the risk of combustion and explosion. Therefore, when storing and using, it is necessary to avoid contact with these dangerous chemicals.
Second, storage conditions are quite critical. It should be stored in a cool and well-ventilated place, away from fire and heat sources. Because it is volatile, if the storage environment temperature is too high, it will accelerate volatilization, not only lose materials, but also accumulate in the air to form flammable and explosive mixed gases. At the same time, it is necessary to ensure that the storage container is tightly sealed to prevent it from reacting with moisture, oxygen and other components in the air, which will affect the quality.
Third, the safety protection during use should not be underestimated. It is necessary to wear appropriate protective equipment, such as protective glasses, gloves, gas masks, etc. Because it may cause irritation and damage to the skin, eyes, and respiratory tract. If you accidentally contact the skin, you should immediately rinse with a lot of water. If you contact the eyes, you need to seek medical attention in time after rinsing. At the operating site, it is necessary to ensure good ventilation to avoid the accumulation of its volatile gases in the air.
Fourth, during transportation, relevant regulations on the transportation of hazardous chemicals must be followed. Use compliant transportation tools, and do a good job of marking and protective measures to prevent package damage due to bumps, collisions, etc. during transportation, resulting in leakage accidents.
In short, when using 1 + -bromo-3- (triethylmethyl) benzene, it is necessary to pay great attention to its chemical properties, storage, safety protection and transportation, and operate in strict accordance with regulations to ensure personnel safety and smooth production.
First, it is related to its chemical properties. This compound has certain reactivity, and when it encounters strong oxidants, strong acids and other substances, it is easy to cause violent chemical reactions, or the risk of combustion and explosion. Therefore, when storing and using, it is necessary to avoid contact with these dangerous chemicals.
Second, storage conditions are quite critical. It should be stored in a cool and well-ventilated place, away from fire and heat sources. Because it is volatile, if the storage environment temperature is too high, it will accelerate volatilization, not only lose materials, but also accumulate in the air to form flammable and explosive mixed gases. At the same time, it is necessary to ensure that the storage container is tightly sealed to prevent it from reacting with moisture, oxygen and other components in the air, which will affect the quality.
Third, the safety protection during use should not be underestimated. It is necessary to wear appropriate protective equipment, such as protective glasses, gloves, gas masks, etc. Because it may cause irritation and damage to the skin, eyes, and respiratory tract. If you accidentally contact the skin, you should immediately rinse with a lot of water. If you contact the eyes, you need to seek medical attention in time after rinsing. At the operating site, it is necessary to ensure good ventilation to avoid the accumulation of its volatile gases in the air.
Fourth, during transportation, relevant regulations on the transportation of hazardous chemicals must be followed. Use compliant transportation tools, and do a good job of marking and protective measures to prevent package damage due to bumps, collisions, etc. during transportation, resulting in leakage accidents.
In short, when using 1 + -bromo-3- (triethylmethyl) benzene, it is necessary to pay great attention to its chemical properties, storage, safety protection and transportation, and operate in strict accordance with regulations to ensure personnel safety and smooth production.
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