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Benzene, 1-Chloro-3-(Trifluoromethyl)-5-[1-(Trifluoromethyl)Ethenyl]-
Linshang Chemical
|
HS Code |
991190 |
| Chemical Formula | C9H4ClF7 |
| Molecular Weight | 282.57 |
| Appearance | Unknown, likely a colorless to pale - yellow liquid |
| Boiling Point | Unknown |
| Melting Point | Unknown |
| Density | Unknown |
| Solubility | Solubility in water is likely low, may be soluble in organic solvents |
| Vapor Pressure | Unknown |
| Flash Point | Unknown |
| Odor | Unknown, potentially has a characteristic halogenated - aromatic odor |
As an accredited Benzene, 1-Chloro-3-(Trifluoromethyl)-5-[1-(Trifluoromethyl)Ethenyl]- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100 - gram bottle packaging for 1 - chloro - 3 - (trifluoromethyl)-5 - [1 - (trifluoromethyl)ethenyl] benzene. |
| Storage | **Storage of 1 - chloro - 3 - (trifluoromethyl)-5 - [1 - (trifluoromethyl)ethenyl]benzene**: Store this chemical in a cool, well - ventilated area away from heat, sparks, and open flames. Keep it in a tightly sealed container, preferably made of corrosion - resistant materials. Avoid contact with oxidizing agents. Store in a dedicated chemical storage cabinet, segregated from incompatible substances to prevent potential reactions. |
| Shipping | The chemical "Benzene, 1 - chloro - 3 - (trifluoromethyl)-5 - [1 - (trifluoromethyl)ethenyl]" must be shipped in accordance with hazardous material regulations. Use proper packaging to prevent leaks, and ensure carriers are trained for such chemicals. |
Competitive Benzene, 1-Chloro-3-(Trifluoromethyl)-5-[1-(Trifluoromethyl)Ethenyl]- 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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What are the physical properties of 1-chloro-3- (trifluoromethyl) -5- [1- (trifluoromethyl) vinyl] benzene?
The physical properties of 1 + -alkane-3- (triethylmethyl) -5- [1- (triethylmethyl) isobutyl] benzene are particularly important, which is related to its application in many fields.
First of all, under normal temperature and pressure, it is mostly a colorless and transparent liquid, with a pure texture and no impurities, just like clear water. Under light, it shines slightly and is quite smart.
Its smell exudes a relatively special aromatic smell, but this fragrance is not as rich and sweet as ordinary flowers, but a relatively light and unique fragrance, which can be smelled slightly fresh, but not too pungent, giving people a different olfactory experience.
The boiling point has been determined by many researchers and is within a specific temperature range. This boiling point characteristic makes it have a specific performance in chemical operations such as distillation and separation. When the temperature gradually rises to near the boiling point, it can be seen that it slowly converts from liquid to gas, and the molecular movement intensifies, breaking free from the liquid phase.
In terms of melting point, it also has its fixed value. Once the ambient temperature drops below the melting point, the substance will gradually solidify from liquid to solid. When the shape changes, the molecular arrangement changes from relatively disordered to regular and orderly, like a soldier's array, orderly.
Density is also one of its important physical properties. Compared with common solvents, it has a specific density value. This value determines its position distribution in the mixed system. If mixed with less dense substances, it often resides in the lower layer; conversely, if mixed with higher density, it will float to the upper layer. This property is quite useful in separation, extraction and other operations.
In terms of solubility, it has good solubility in organic solvents such as ethanol and ether, and can be miscible with them to form a uniform and stable solution. However, in water, its solubility is poor, and it mostly exists in a layered state. The upper layer is an aqueous phase, and the lower layer is an organic phase. This phenomenon is closely related to factors such as molecular polarity.
In summary, the many physical properties of 1 + -alkane-3- (triethyl methyl) -5- [1- (triethyl) isobutyl] benzene have their own unique characteristics. They play a significant role in many fields such as chemical industry and scientific research, providing an important basis for related operations and research.
First of all, under normal temperature and pressure, it is mostly a colorless and transparent liquid, with a pure texture and no impurities, just like clear water. Under light, it shines slightly and is quite smart.
Its smell exudes a relatively special aromatic smell, but this fragrance is not as rich and sweet as ordinary flowers, but a relatively light and unique fragrance, which can be smelled slightly fresh, but not too pungent, giving people a different olfactory experience.
The boiling point has been determined by many researchers and is within a specific temperature range. This boiling point characteristic makes it have a specific performance in chemical operations such as distillation and separation. When the temperature gradually rises to near the boiling point, it can be seen that it slowly converts from liquid to gas, and the molecular movement intensifies, breaking free from the liquid phase.
In terms of melting point, it also has its fixed value. Once the ambient temperature drops below the melting point, the substance will gradually solidify from liquid to solid. When the shape changes, the molecular arrangement changes from relatively disordered to regular and orderly, like a soldier's array, orderly.
Density is also one of its important physical properties. Compared with common solvents, it has a specific density value. This value determines its position distribution in the mixed system. If mixed with less dense substances, it often resides in the lower layer; conversely, if mixed with higher density, it will float to the upper layer. This property is quite useful in separation, extraction and other operations.
In terms of solubility, it has good solubility in organic solvents such as ethanol and ether, and can be miscible with them to form a uniform and stable solution. However, in water, its solubility is poor, and it mostly exists in a layered state. The upper layer is an aqueous phase, and the lower layer is an organic phase. This phenomenon is closely related to factors such as molecular polarity.
In summary, the many physical properties of 1 + -alkane-3- (triethyl methyl) -5- [1- (triethyl) isobutyl] benzene have their own unique characteristics. They play a significant role in many fields such as chemical industry and scientific research, providing an important basis for related operations and research.
What are the chemical properties of 1-chloro-3- (trifluoromethyl) -5- [1- (trifluoromethyl) vinyl] benzene?
1 + -Alkane-3- (triethylmethyl) -5- [1- (triethylmethyl) ethynyl] benzene is an organic compound with rich chemical properties.
In terms of its stability, the carbon-carbon single bond and carbon-hydrogen single bond in this compound have relatively high stability. The carbon-carbon single bond has high energy, which endows the molecule with certain stability and is not easy to spontaneously break under normal conditions. However, the carbon-carbon triple bond is quite active. The carbon-carbon triple bond contains two pi bonds, and the electron cloud density is high, which is vulnerable to electrophilic attack and addition reaction. For example, it can be added with halogen elements (such as bromine tetrachloride solution) to generate bromine-containing addition products. This is the electrophilic addition reaction process, because the bromine molecule is polarized by π electron cloud when it is close to the carbon-carbon triple bond. The positively charged end first binds to the carbon-carbon triple bond, and then the negatively charged part is connected to it.
Furthermore, although the alkyl part of the compound is relatively stable, free radical substitution reactions can occur under high temperature, light or initiator conditions. For example, when irradiated with chlorine, the hydrogen atoms on the alkyl group can be replaced by chlorine atoms. This is because the light makes the chlorine molecules split into chlorine radicals, and the chlorine radicals capture the hydrogen atoms on the alkyl group to form hydrogen chloride and alkyl radicals. The alkyl radicals then react with chlorine to form chloroalkanes.
The benzene ring structure also gives this compound unique chemical properties. The benzene ring has a conjugated large π bond, and the electron cloud is highly delocalized and relatively stable. However, the benzene ring can undergo electrophilic substitution reactions because its large π bond electron clouds are distributed on the upper and lower sides of the benzene ring, which are easily attacked by electrophilic reagents. For example, when there is a catalyst (such as ferric chloride), it can undergo bromination reaction with bromine, and bromine atoms replace hydrogen atoms on the benz
In addition, the specific substituents (triethyl, etc.) in the compound will have electronic and spatial effects on its chemical properties. The substituents of the power supply will change the electron cloud density of the benzene ring or the carbon-carbon triple bond, thereby affecting the reactivity and reaction check point selectivity.
In terms of its stability, the carbon-carbon single bond and carbon-hydrogen single bond in this compound have relatively high stability. The carbon-carbon single bond has high energy, which endows the molecule with certain stability and is not easy to spontaneously break under normal conditions. However, the carbon-carbon triple bond is quite active. The carbon-carbon triple bond contains two pi bonds, and the electron cloud density is high, which is vulnerable to electrophilic attack and addition reaction. For example, it can be added with halogen elements (such as bromine tetrachloride solution) to generate bromine-containing addition products. This is the electrophilic addition reaction process, because the bromine molecule is polarized by π electron cloud when it is close to the carbon-carbon triple bond. The positively charged end first binds to the carbon-carbon triple bond, and then the negatively charged part is connected to it.
Furthermore, although the alkyl part of the compound is relatively stable, free radical substitution reactions can occur under high temperature, light or initiator conditions. For example, when irradiated with chlorine, the hydrogen atoms on the alkyl group can be replaced by chlorine atoms. This is because the light makes the chlorine molecules split into chlorine radicals, and the chlorine radicals capture the hydrogen atoms on the alkyl group to form hydrogen chloride and alkyl radicals. The alkyl radicals then react with chlorine to form chloroalkanes.
The benzene ring structure also gives this compound unique chemical properties. The benzene ring has a conjugated large π bond, and the electron cloud is highly delocalized and relatively stable. However, the benzene ring can undergo electrophilic substitution reactions because its large π bond electron clouds are distributed on the upper and lower sides of the benzene ring, which are easily attacked by electrophilic reagents. For example, when there is a catalyst (such as ferric chloride), it can undergo bromination reaction with bromine, and bromine atoms replace hydrogen atoms on the benz
In addition, the specific substituents (triethyl, etc.) in the compound will have electronic and spatial effects on its chemical properties. The substituents of the power supply will change the electron cloud density of the benzene ring or the carbon-carbon triple bond, thereby affecting the reactivity and reaction check point selectivity.
What are the main uses of 1-chloro-3- (trifluoromethyl) -5- [1- (trifluoromethyl) vinyl] benzene?
The main use of 1 + - + - 3- (triethyl) -5- [1- (triethyl) ethoxy methyl] benzene is in the field of chemical synthesis.
In terms of chemical synthesis, due to its special chemical properties, it is often used as an important medium for the synthesis of specific chemical compounds. For example, the synthesis of some chemical compounds used to treat cardiovascular diseases involves the use of this material as the starting material, and the multi-step reaction of chemical molecules. Through precise control of the reaction components and chemical modifications, it can be derived from compounds with specific biological activities to meet the needs of the target of the chemical.
In the field of chemical synthesis, this compound can be filled with chemical components. For example, in the process of synthesizing materials with special optical properties, the properties of benzene and substituents can be used to introduce specific sub-effects and space resistance to control the light absorption and light absorption properties of materials. Furthermore, in the total synthesis of natural compounds, it is also often used as an important model to help complete the construction of the molecular skeleton of natural compounds and promote the development of synthesis.
In terms of chemical synthesis, due to its special chemical properties, it is often used as an important medium for the synthesis of specific chemical compounds. For example, the synthesis of some chemical compounds used to treat cardiovascular diseases involves the use of this material as the starting material, and the multi-step reaction of chemical molecules. Through precise control of the reaction components and chemical modifications, it can be derived from compounds with specific biological activities to meet the needs of the target of the chemical.
In the field of chemical synthesis, this compound can be filled with chemical components. For example, in the process of synthesizing materials with special optical properties, the properties of benzene and substituents can be used to introduce specific sub-effects and space resistance to control the light absorption and light absorption properties of materials. Furthermore, in the total synthesis of natural compounds, it is also often used as an important model to help complete the construction of the molecular skeleton of natural compounds and promote the development of synthesis.
What are the methods for preparing 1-chloro-3- (trifluoromethyl) -5- [1- (trifluoromethyl) vinyl] benzene?
To prepare 1-bromo-3- (triethyl) -5- [1 - (triethyl) propargyl] benzene, the method is as follows:
First, all raw materials must be prepared, such as compounds containing triethyl, propargyl-related reagents and brominating agents, etc., to ensure its purity and quality.
In a suitable reaction vessel, put in a substrate containing triethyl methyl according to a specific ratio. This substrate should be selected with caution, and its reactivity and structural stability should be considered. Then, under the protection of an inert gas atmosphere, slowly add propargyl reagents. Inert gas can create an oxygen-free environment to avoid the growth of side reactions. During the reaction, the temperature is strictly controlled, and the appropriate temperature range is adjusted according to the characteristics of the substrate and the reagent. Either low temperature is used to stabilize the reaction rate, or high temperature is used to promote the reaction to proceed efficiently. At the same time, stirring is used to make the reactants fully contact and accelerate the reaction process.
After the propargyl reaction is completed, the reaction mixture is separated and purified. The column chromatography can be used to select the appropriate eluent according to the polarity of the compound, and the target product can be separated from the impurities.
Then, the bromination step is carried out. Select the appropriate brominating agent, such as liquid bromine, N-bromosuccinimide (NBS), etc. If using liquid bromine, the operation must be cautious, because it is highly corrosive and volatile. The brominating agent is added dropwise to the purified propargyl-containing product solution, and the reaction progress is monitored synchronously. The end point of the reaction can be determined by thin-layer chromatography (TLC).
After the bromination reaction is complete, the product is separated and purified again. By recrystallization, a suitable solvent can be selected to allow the product to crystallize and precipitate from the solution, remove residual impurities, and obtain pure 1-bromo-3- (triethyl) -5- [1 - (triethyl) propargyl] benzene. Each step requires careful operation and attention to the control of reaction conditions in order to improve the yield and purity of the product.
First, all raw materials must be prepared, such as compounds containing triethyl, propargyl-related reagents and brominating agents, etc., to ensure its purity and quality.
In a suitable reaction vessel, put in a substrate containing triethyl methyl according to a specific ratio. This substrate should be selected with caution, and its reactivity and structural stability should be considered. Then, under the protection of an inert gas atmosphere, slowly add propargyl reagents. Inert gas can create an oxygen-free environment to avoid the growth of side reactions. During the reaction, the temperature is strictly controlled, and the appropriate temperature range is adjusted according to the characteristics of the substrate and the reagent. Either low temperature is used to stabilize the reaction rate, or high temperature is used to promote the reaction to proceed efficiently. At the same time, stirring is used to make the reactants fully contact and accelerate the reaction process.
After the propargyl reaction is completed, the reaction mixture is separated and purified. The column chromatography can be used to select the appropriate eluent according to the polarity of the compound, and the target product can be separated from the impurities.
Then, the bromination step is carried out. Select the appropriate brominating agent, such as liquid bromine, N-bromosuccinimide (NBS), etc. If using liquid bromine, the operation must be cautious, because it is highly corrosive and volatile. The brominating agent is added dropwise to the purified propargyl-containing product solution, and the reaction progress is monitored synchronously. The end point of the reaction can be determined by thin-layer chromatography (TLC).
After the bromination reaction is complete, the product is separated and purified again. By recrystallization, a suitable solvent can be selected to allow the product to crystallize and precipitate from the solution, remove residual impurities, and obtain pure 1-bromo-3- (triethyl) -5- [1 - (triethyl) propargyl] benzene. Each step requires careful operation and attention to the control of reaction conditions in order to improve the yield and purity of the product.
What are the precautions for storing and transporting 1-chloro-3- (trifluoromethyl) -5- [1- (trifluoromethyl) vinyl] benzene?
This is related to the precautions of "1-alkane-3- (triethyl) -5- [1 - (triethyl) ethynyl] benzene" during storage and transportation. When storing and transporting its contents, be careful to pay attention to the following things:
First, the storage environment must be carefully selected. A cool and well-ventilated place should be found to avoid direct sunlight, due to light or cause adverse reactions. Temperature must also be properly controlled. Excessive temperature may cause chemical instability and lead to danger. Humidity should not be underestimated. Excessive humidity or dampness of the substance will affect its quality and stability.
Second, the choice of storage containers is crucial. A specially adapted container should be used. The material of the container must not chemically react with "1-alkane-3- (triethyl) -5- [1 - (triethyl) ethynyl] benzene". The sealing must be good to prevent material leakage, and the key information such as its name and characteristics should be clearly marked on the outside of the container.
Third, during transportation, relevant regulations and standards must be strictly adhered to. Transportation vehicles should be equipped with appropriate protective and emergency equipment, such as fire extinguishing equipment, leakage emergency treatment tools, etc. When loading and unloading, the operation must be gentle to avoid violent vibration and impact, so as to prevent material leakage caused by package damage.
Fourth, personnel management cannot be ignored. Those involved in storage and transportation must have professional training and be familiar with the characteristics, hazards and emergency treatment methods of the substance. When working, protective equipment should be worn in accordance with regulations, such as protective clothing, protective gloves, protective glasses, etc., to ensure their own safety.
Fifth, it is also necessary to formulate a sound emergency plan. In case of emergencies such as leaks and fires, emergency response can be carried out quickly and orderly to minimize losses and hazards.
First, the storage environment must be carefully selected. A cool and well-ventilated place should be found to avoid direct sunlight, due to light or cause adverse reactions. Temperature must also be properly controlled. Excessive temperature may cause chemical instability and lead to danger. Humidity should not be underestimated. Excessive humidity or dampness of the substance will affect its quality and stability.
Second, the choice of storage containers is crucial. A specially adapted container should be used. The material of the container must not chemically react with "1-alkane-3- (triethyl) -5- [1 - (triethyl) ethynyl] benzene". The sealing must be good to prevent material leakage, and the key information such as its name and characteristics should be clearly marked on the outside of the container.
Third, during transportation, relevant regulations and standards must be strictly adhered to. Transportation vehicles should be equipped with appropriate protective and emergency equipment, such as fire extinguishing equipment, leakage emergency treatment tools, etc. When loading and unloading, the operation must be gentle to avoid violent vibration and impact, so as to prevent material leakage caused by package damage.
Fourth, personnel management cannot be ignored. Those involved in storage and transportation must have professional training and be familiar with the characteristics, hazards and emergency treatment methods of the substance. When working, protective equipment should be worn in accordance with regulations, such as protective clothing, protective gloves, protective glasses, etc., to ensure their own safety.
Fifth, it is also necessary to formulate a sound emergency plan. In case of emergencies such as leaks and fires, emergency response can be carried out quickly and orderly to minimize losses and hazards.
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