Linshang Chemical
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2,4-Dichloro-1-(Trifluoromethyl)Benzene
Linshang Chemical
|
HS Code |
768615 |
| Chemical Formula | C7H3Cl2F3 |
| Molar Mass | 215.00 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 184 - 186 °C |
| Density | 1.45 g/cm³ |
| Solubility In Water | Insoluble |
| Flash Point | 69 °C |
| Logp | 3.84 |
As an accredited 2,4-Dichloro-1-(Trifluoromethyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500 - gram bottle packaging for 2,4 - dichloro - 1 - (trifluoromethyl)benzene chemical. |
| Storage | 2,4 - dichloro - 1 - (trifluoromethyl)benzene should be stored in a cool, well - ventilated area, away from heat sources and open flames. Keep it in a tightly sealed container, preferably made of corrosion - resistant materials. Store it separately from oxidizing agents and incompatible substances to prevent chemical reactions. |
| Shipping | 2,4 - dichloro - 1 - (trifluoromethyl)benzene is shipped in accordance with strict hazardous chemicals regulations. It's typically in sealed, corrosion - resistant containers, transported by specialized carriers to ensure safety during transit. |
Competitive 2,4-Dichloro-1-(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 2,4-Dichloro-1-(Trifluoromethyl)Benzene in China?
As a trusted 2,4-Dichloro-1-(Trifluoromethyl)Benzene manufacturer, we deliver:
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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 2,4-Dichloro-1-(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 2,4-dichloro-1- (trifluoromethyl) benzene?
2% 2C4-difluoro-1- (triethoxysilyl) benzene has a wide range of uses. In the field of chemical industry, it is often used as a raw material for the preparation of special silicone materials. With its silicon base and fluorine atoms, it can give the material unique properties.
Silicon has good film-forming and adhesion, which can make the material tightly bond with the substrate. The fluorine atom has high electronegativity, which can increase the chemical stability, weather resistance and low surface energy of the material. The silicone material obtained by this method can improve the protective performance and durability of the product in paints and adhesives.
In the field of electronics, it is also important. Due to its special structure, it can be used to prepare electronic packaging materials. With its excellent insulation and thermal stability, it can protect electronic components from the influence of the external environment and ensure the stable operation of electronic equipment. And its low surface energy can help electronic components dissipate heat and improve the reliability of equipment.
In terms of optical materials, it also shows its unique value. Due to the existence of fluorine atoms, the refractive index of the material can be adjusted, which can be used to prepare optical components such as optical lenses and optical fibers, which can improve optical properties and improve image quality.
In addition, it may also be used in the synthesis of pharmaceutical intermediates. Its special structure can introduce specific functional groups into drug molecules, which can change the physicochemical properties of drugs, such as solubility and stability, and then affect the biological activity and pharmacokinetic properties of drugs.
Silicon has good film-forming and adhesion, which can make the material tightly bond with the substrate. The fluorine atom has high electronegativity, which can increase the chemical stability, weather resistance and low surface energy of the material. The silicone material obtained by this method can improve the protective performance and durability of the product in paints and adhesives.
In the field of electronics, it is also important. Due to its special structure, it can be used to prepare electronic packaging materials. With its excellent insulation and thermal stability, it can protect electronic components from the influence of the external environment and ensure the stable operation of electronic equipment. And its low surface energy can help electronic components dissipate heat and improve the reliability of equipment.
In terms of optical materials, it also shows its unique value. Due to the existence of fluorine atoms, the refractive index of the material can be adjusted, which can be used to prepare optical components such as optical lenses and optical fibers, which can improve optical properties and improve image quality.
In addition, it may also be used in the synthesis of pharmaceutical intermediates. Its special structure can introduce specific functional groups into drug molecules, which can change the physicochemical properties of drugs, such as solubility and stability, and then affect the biological activity and pharmacokinetic properties of drugs.
What are the physical properties of 2,4-dichloro-1- (trifluoromethyl) benzene?
2% 2C4-difluoro-1- (triethylmethyl) benzene is an organic compound. Its physical properties are quite unique, and I would like to describe them in detail for you.
In terms of its properties, under room temperature and pressure, this substance is mostly in the form of a colorless and transparent liquid. It is clear and pure in appearance. It is like a clear spring without special color, but it also shows its unique quality.
Smell it, it has a special smell. This smell is neither fragrant nor pungent, but it has its own unique smell, just like a unique logo hidden in the world. Although it is not publicized, it is difficult to ignore.
Its boiling point is also one of the important physical properties. Under appropriate pressure conditions, its boiling point is within a specific range, and this boiling point value is of great significance for its existence and application in different environments. When the external temperature rises to the boiling point, the substance will change from liquid to gaseous state, starting its journey in the gaseous phase.
The melting point also has its specific value. When the temperature drops below the melting point, 2% 2C4-difluoro-1- (triethylmethyl) benzene will condense from liquid to solid state, just like time solidification, giving it a different form.
As for density, compared to water, it has a specific proportional relationship. Its density is either greater than or less than that of water. This characteristic determines that when it is mixed with water, it either sinks at the bottom or floats on the water surface, which becomes an important basis for identifying its characteristics.
Solubility is also a property that cannot be ignored. In organic solvents, such as common ethanol, ether, etc., its solubility is good and can be mixed with it, just like water emulsion; in water, its solubility may be different, slightly soluble, or insoluble, depending on the interaction between its molecular structure and water molecules.
These physical properties play a crucial role in the application of 2% 2C4-difluoro-1- (triethylmethyl) benzene in many fields such as chemical synthesis and material preparation, laying a solid foundation for its existence and application in the world.
In terms of its properties, under room temperature and pressure, this substance is mostly in the form of a colorless and transparent liquid. It is clear and pure in appearance. It is like a clear spring without special color, but it also shows its unique quality.
Smell it, it has a special smell. This smell is neither fragrant nor pungent, but it has its own unique smell, just like a unique logo hidden in the world. Although it is not publicized, it is difficult to ignore.
Its boiling point is also one of the important physical properties. Under appropriate pressure conditions, its boiling point is within a specific range, and this boiling point value is of great significance for its existence and application in different environments. When the external temperature rises to the boiling point, the substance will change from liquid to gaseous state, starting its journey in the gaseous phase.
The melting point also has its specific value. When the temperature drops below the melting point, 2% 2C4-difluoro-1- (triethylmethyl) benzene will condense from liquid to solid state, just like time solidification, giving it a different form.
As for density, compared to water, it has a specific proportional relationship. Its density is either greater than or less than that of water. This characteristic determines that when it is mixed with water, it either sinks at the bottom or floats on the water surface, which becomes an important basis for identifying its characteristics.
Solubility is also a property that cannot be ignored. In organic solvents, such as common ethanol, ether, etc., its solubility is good and can be mixed with it, just like water emulsion; in water, its solubility may be different, slightly soluble, or insoluble, depending on the interaction between its molecular structure and water molecules.
These physical properties play a crucial role in the application of 2% 2C4-difluoro-1- (triethylmethyl) benzene in many fields such as chemical synthesis and material preparation, laying a solid foundation for its existence and application in the world.
What are the chemical properties of 2,4-dichloro-1- (trifluoromethyl) benzene?
2% 2C4 -difluoro-1- (triethylmethyl) benzene is an organic compound with unique chemical properties, so let me tell you one by one.
In this compound, the fluorine atom is connected to the benzene ring, giving it a certain chemical activity. Fluorine atoms have high electronegativity, which will affect the distribution of electron clouds in the benzene ring, causing the electron cloud density of the benzene ring to decrease. Therefore, its electrophilic substitution reactivity is lower than that of benzene. When confronted with the attack of electrophilic reagents, the reaction conditions of this compound are often more severe, and the required temperature, catalyst and other conditions may be different from common benzene compounds.
The presence of triethyl methyl also affects its chemical properties. Triethyl is the power supply group, which can increase the electron cloud density of the benzene ring. Under this action, when the electrophilic substitution reaction is carried out, the electrophilic reagents are more inclined to attack the ortho and para-sites of the benzene ring.
From the perspective of stability, the steric resistance of the compound increases due to the existence of fluorine atoms and triethyl methyl. The large steric resistance changes the interaction between molecules, which affects its physical and chemical properties to a certain extent, such as boiling point, melting point, etc. And the steric resistance will affect the chemical reaction process. When some reagents are close to the reaction check point, they may be hindered, resulting in a change in the reaction rate.
In addition, under specific conditions, this compound may undergo substitution, addition and other reactions. In the substitution reaction, the hydrogen atom on the benzene ring may be replaced by other groups; in the addition reaction, the unsaturated bond such as double bond or triple bond can be added with the reagent.
In short, the chemical properties of 2% 2C4 -difluoro-1- (triethylmethyl) benzene are molded by the fluorine atom and triethylmethyl, and may have unique applications and reaction characteristics in the field of organic synthesis.
In this compound, the fluorine atom is connected to the benzene ring, giving it a certain chemical activity. Fluorine atoms have high electronegativity, which will affect the distribution of electron clouds in the benzene ring, causing the electron cloud density of the benzene ring to decrease. Therefore, its electrophilic substitution reactivity is lower than that of benzene. When confronted with the attack of electrophilic reagents, the reaction conditions of this compound are often more severe, and the required temperature, catalyst and other conditions may be different from common benzene compounds.
The presence of triethyl methyl also affects its chemical properties. Triethyl is the power supply group, which can increase the electron cloud density of the benzene ring. Under this action, when the electrophilic substitution reaction is carried out, the electrophilic reagents are more inclined to attack the ortho and para-sites of the benzene ring.
From the perspective of stability, the steric resistance of the compound increases due to the existence of fluorine atoms and triethyl methyl. The large steric resistance changes the interaction between molecules, which affects its physical and chemical properties to a certain extent, such as boiling point, melting point, etc. And the steric resistance will affect the chemical reaction process. When some reagents are close to the reaction check point, they may be hindered, resulting in a change in the reaction rate.
In addition, under specific conditions, this compound may undergo substitution, addition and other reactions. In the substitution reaction, the hydrogen atom on the benzene ring may be replaced by other groups; in the addition reaction, the unsaturated bond such as double bond or triple bond can be added with the reagent.
In short, the chemical properties of 2% 2C4 -difluoro-1- (triethylmethyl) benzene are molded by the fluorine atom and triethylmethyl, and may have unique applications and reaction characteristics in the field of organic synthesis.
What is the preparation method of 2,4-dichloro-1- (trifluoromethyl) benzene?
To prepare 2,4-difluoro-1- (trifluoromethyl) benzene, the following method can be used.
First take appropriate starting materials, preferably benzene compounds, because the benzene ring structure can lay the foundation for subsequent reactions. The introduction of specific substituents on the benzene ring is a key step. The halogenation reaction can be used to carefully adjust the reaction conditions, such as temperature, pressure, and the type and dosage of catalysts, so that fluorine atoms can be introduced into the benzene ring at specific positions to achieve the purpose of generating 2,4-difluorobenzene derivatives. In this process, the choice of halogenation reagents is very important. It is necessary to choose those with suitable activity and good selectivity to introduce fluorine atoms accurately at the 2,4 position of the benzene ring.
Then, for the obtained 2,4-difluorobenzene derivative, trifluoromethyl is introduced. Many methods can be used in this step, such as using reagents containing trifluoromethyl, under suitable reaction conditions, by means of nucleophilic substitution reaction or free radical reaction, the trifluoromethyl is successfully connected to the benzene ring, and the connection position is precisely 1. In this case, the control of the reaction conditions is critical to success or failure, and the reaction temperature, reaction time, and the proportion of reactants must be strictly controlled in order to improve the yield and purity of the target product.
After the reaction is completed, the product needs to be separated and purified. Conventional separation methods such as distillation, extraction, and column chromatography can be used to effectively separate the target product from the reaction mixture and remove impurities to obtain high-purity 2,4-difluoro-1- (trifluoromethyl) benzene. Each step requires fine operation, and a slight error may affect the quality and yield of the product. In this way, following the above steps and performing them in an orderly manner, the required 2,4-difluoro-1- (trifluoromethyl) benzene can be prepared.
First take appropriate starting materials, preferably benzene compounds, because the benzene ring structure can lay the foundation for subsequent reactions. The introduction of specific substituents on the benzene ring is a key step. The halogenation reaction can be used to carefully adjust the reaction conditions, such as temperature, pressure, and the type and dosage of catalysts, so that fluorine atoms can be introduced into the benzene ring at specific positions to achieve the purpose of generating 2,4-difluorobenzene derivatives. In this process, the choice of halogenation reagents is very important. It is necessary to choose those with suitable activity and good selectivity to introduce fluorine atoms accurately at the 2,4 position of the benzene ring.
Then, for the obtained 2,4-difluorobenzene derivative, trifluoromethyl is introduced. Many methods can be used in this step, such as using reagents containing trifluoromethyl, under suitable reaction conditions, by means of nucleophilic substitution reaction or free radical reaction, the trifluoromethyl is successfully connected to the benzene ring, and the connection position is precisely 1. In this case, the control of the reaction conditions is critical to success or failure, and the reaction temperature, reaction time, and the proportion of reactants must be strictly controlled in order to improve the yield and purity of the target product.
After the reaction is completed, the product needs to be separated and purified. Conventional separation methods such as distillation, extraction, and column chromatography can be used to effectively separate the target product from the reaction mixture and remove impurities to obtain high-purity 2,4-difluoro-1- (trifluoromethyl) benzene. Each step requires fine operation, and a slight error may affect the quality and yield of the product. In this way, following the above steps and performing them in an orderly manner, the required 2,4-difluoro-1- (trifluoromethyl) benzene can be prepared.
What are the precautions for using 2,4-dichloro-1- (trifluoromethyl) benzene?
2% 2C4-dihydro-1- (triethylmethyl) naphthalene There are many things to pay attention to when using this product.
The first priority is safety. This substance may be toxic and irritating. When operating, be sure to wear appropriate protective equipment, such as protective clothing, gloves, goggles, etc., to prevent skin contact with it and avoid inhaling its volatile gas. If you are accidentally exposed, you should immediately rinse with plenty of water and seek medical treatment according to the specific situation.
Store it for the second time. It should be stored in a cool, dry and well-ventilated place, away from fire and heat sources, and protected from direct sunlight, because it may be flammable or easily decomposed by heat, and should be stored separately from oxidants, acids, etc. to avoid dangerous chemical reactions.
Furthermore, the access process should be strictly operated according to the specifications. Precisely control the dosage to avoid waste and environmental pollution caused by excessive use. The instruments used should be clean and dry to prevent impurities from affecting their properties and reaction results.
In addition, the experimental environment should ensure smooth ventilation, and the volatile harmful gases should be discharged in time to reduce the concentration in the air to ensure safety. If used in industrial production, the waste discharged should also be properly disposed of to ensure that it meets environmental standards and cannot be discarded or discharged at will to avoid pollution to the surrounding environment. Only by paying careful attention to the above points throughout the use can the purpose of use be achieved, and the safety of personnel and the environment are not endangered.
The first priority is safety. This substance may be toxic and irritating. When operating, be sure to wear appropriate protective equipment, such as protective clothing, gloves, goggles, etc., to prevent skin contact with it and avoid inhaling its volatile gas. If you are accidentally exposed, you should immediately rinse with plenty of water and seek medical treatment according to the specific situation.
Store it for the second time. It should be stored in a cool, dry and well-ventilated place, away from fire and heat sources, and protected from direct sunlight, because it may be flammable or easily decomposed by heat, and should be stored separately from oxidants, acids, etc. to avoid dangerous chemical reactions.
Furthermore, the access process should be strictly operated according to the specifications. Precisely control the dosage to avoid waste and environmental pollution caused by excessive use. The instruments used should be clean and dry to prevent impurities from affecting their properties and reaction results.
In addition, the experimental environment should ensure smooth ventilation, and the volatile harmful gases should be discharged in time to reduce the concentration in the air to ensure safety. If used in industrial production, the waste discharged should also be properly disposed of to ensure that it meets environmental standards and cannot be discarded or discharged at will to avoid pollution to the surrounding environment. Only by paying careful attention to the above points throughout the use can the purpose of use be achieved, and the safety of personnel and the environment are not endangered.
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