Linshang Chemical
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1-Chloro-4-[(Trifluoromethyl)Sulfanyl]Benzene
Linshang Chemical
|
HS Code |
798830 |
| Chemical Formula | C7H4ClF3S |
| Molecular Weight | 228.62 |
As an accredited 1-Chloro-4-[(Trifluoromethyl)Sulfanyl]Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100 - gram bottles of 1 - chloro - 4 - [(trifluoromethyl)sulfanyl]benzene, well - sealed. |
| Storage | 1 - Chloro - 4 - [(trifluoromethyl)sulfanyl]benzene should be stored in a cool, well - ventilated area, away from heat sources and ignition points. Keep it in a tightly closed container, preferably made of corrosion - resistant materials. Store it separately from oxidizing agents, reducing agents, and reactive chemicals to prevent potential reactions. Follow local safety regulations for proper storage. |
| Shipping | 1 - chloro - 4 - [(trifluoromethyl)sulfanyl]benzene is shipped in sealed, corrosion - resistant containers. Strict compliance with hazardous chemical shipping regulations ensures safe transportation to prevent leakage and environmental risks. |
Competitive 1-Chloro-4-[(Trifluoromethyl)Sulfanyl]Benzene prices that fit your budget—flexible terms and customized quotes for every order.
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As a leading 1-Chloro-4-[(Trifluoromethyl)Sulfanyl]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 is the main use of 1-chloro-4- [ (trifluoromethyl) sulfanyl] benzene
1 - chloro - 4 - [ (trifluoromethyl) sulfanyl] benzene, the Chinese name is often called 4 - (trifluoromethyl) chlorobenzene. This substance is widely used in chemical synthesis.
First, it is a key intermediate in the field of pharmaceutical synthesis. Taking the preparation of many antibacterial and antiviral drugs as an example, this compound is often relied on as the starting material. Due to its special structure, trifluoromethyl thio has strong electron absorption, which can change the electron cloud distribution of the compound, and then adjust the activity and selectivity of the drug molecule. After a series of chemical reactions, specific functional groups are added, and a molecular structure with specific pharmacological activities can be constructed.
Second, in the field of pesticide creation, it is also an important synthetic building block. Thanks to its characteristics of introducing trifluoromethylthio groups, the synthesized pesticides often have excellent biological activity. It can effectively improve the poisoning ability of pesticides to pests, inhibit weeds, and enhance the environmental adaptability and effectiveness of pesticides. For example, in the development of some new pesticides and herbicides, 4- (trifluoromethylthio) chlorobenzene plays a pivotal role.
Third, it is also applied in the field of materials science. Due to the special physical and chemical properties endowed by its structure, it can participate in the synthesis of functional materials. For example, in the preparation of some optoelectronic materials, the introduction of this structural unit is expected to improve the electrical and optical properties of the materials, laying the foundation for the development of new optoelectronic devices.
In summary, 1-chloro-4- [ (trifluoromethyl) sulfanyl] benzene is an indispensable and important compound in many fields such as medicine, pesticides, materials, etc., promoting the sustainable development and innovation in various fields.
First, it is a key intermediate in the field of pharmaceutical synthesis. Taking the preparation of many antibacterial and antiviral drugs as an example, this compound is often relied on as the starting material. Due to its special structure, trifluoromethyl thio has strong electron absorption, which can change the electron cloud distribution of the compound, and then adjust the activity and selectivity of the drug molecule. After a series of chemical reactions, specific functional groups are added, and a molecular structure with specific pharmacological activities can be constructed.
Second, in the field of pesticide creation, it is also an important synthetic building block. Thanks to its characteristics of introducing trifluoromethylthio groups, the synthesized pesticides often have excellent biological activity. It can effectively improve the poisoning ability of pesticides to pests, inhibit weeds, and enhance the environmental adaptability and effectiveness of pesticides. For example, in the development of some new pesticides and herbicides, 4- (trifluoromethylthio) chlorobenzene plays a pivotal role.
Third, it is also applied in the field of materials science. Due to the special physical and chemical properties endowed by its structure, it can participate in the synthesis of functional materials. For example, in the preparation of some optoelectronic materials, the introduction of this structural unit is expected to improve the electrical and optical properties of the materials, laying the foundation for the development of new optoelectronic devices.
In summary, 1-chloro-4- [ (trifluoromethyl) sulfanyl] benzene is an indispensable and important compound in many fields such as medicine, pesticides, materials, etc., promoting the sustainable development and innovation in various fields.
What are the physical properties of 1-chloro-4- [ (trifluoromethyl) sulfanyl] benzene
1 - chloro - 4 - [ (trifluoromethyl) sulfanyl] benzene, this is an organic compound, which is often described by the world with specific symbols and formulas. Its molecule contains a benzene ring, a benzene ring with one chlorine atom and a four-position [ (trifluoromethyl) sulfanyl] group.
When it comes to the physical properties of this substance, its state is mostly liquid at room temperature and pressure, but it is also affected by environmental factors. Looking at its color, it is either colorless and transparent, or very light in color, and has a specific smell, so the smell is difficult for ordinary people to smell or distinguish.
Its boiling point is related to the intermolecular force. Due to the complex intermolecular force of chlorine, fluorine and other atoms, the boiling point has a unique value. Generally speaking, due to the molecular structure and atomic characteristics, the boiling point may be in a certain temperature range, but the exact value needs to be determined experimentally.
Melting point is also an important physical property, reflecting the molecular lattice arrangement and interaction. This substance is affected by the properties of atoms and groups in the structure, and the molecular arrangement order is affected, and the melting point is also in a specific range.
In terms of solubility, according to the principle of similar miscibility, it is an organic compound. It has good solubility in organic solvents such as benzene, toluene, dichloromethane, etc. Because the molecular structure is similar to that of organic solvents, weak interactions can be formed between molecules, which promotes dissolution. However, the solubility in water is poor. Because water is a polar molecule, it has a large difference in molecular structure and weak interaction with the organic substance, so it is difficult to dissolve.
In addition, the density of this substance is also one of the physical properties. Due to the type and number of atoms in the molecule, its density may be greater or smaller than that of water. The specific value depends on accurate measurement, and the density is affected by temperature. Temperature changes, molecular spacing and motion changes, resulting in density changes.
In summary, the physical properties of 1 - chloro - 4 - [ (trifluoromethyl) sulfanyl] benzene are affected by atoms and groups in the molecular structure, and the properties are interrelated, which is of great significance in chemical research and application fields.
When it comes to the physical properties of this substance, its state is mostly liquid at room temperature and pressure, but it is also affected by environmental factors. Looking at its color, it is either colorless and transparent, or very light in color, and has a specific smell, so the smell is difficult for ordinary people to smell or distinguish.
Its boiling point is related to the intermolecular force. Due to the complex intermolecular force of chlorine, fluorine and other atoms, the boiling point has a unique value. Generally speaking, due to the molecular structure and atomic characteristics, the boiling point may be in a certain temperature range, but the exact value needs to be determined experimentally.
Melting point is also an important physical property, reflecting the molecular lattice arrangement and interaction. This substance is affected by the properties of atoms and groups in the structure, and the molecular arrangement order is affected, and the melting point is also in a specific range.
In terms of solubility, according to the principle of similar miscibility, it is an organic compound. It has good solubility in organic solvents such as benzene, toluene, dichloromethane, etc. Because the molecular structure is similar to that of organic solvents, weak interactions can be formed between molecules, which promotes dissolution. However, the solubility in water is poor. Because water is a polar molecule, it has a large difference in molecular structure and weak interaction with the organic substance, so it is difficult to dissolve.
In addition, the density of this substance is also one of the physical properties. Due to the type and number of atoms in the molecule, its density may be greater or smaller than that of water. The specific value depends on accurate measurement, and the density is affected by temperature. Temperature changes, molecular spacing and motion changes, resulting in density changes.
In summary, the physical properties of 1 - chloro - 4 - [ (trifluoromethyl) sulfanyl] benzene are affected by atoms and groups in the molecular structure, and the properties are interrelated, which is of great significance in chemical research and application fields.
What are the chemical properties of 1-chloro-4- [ (trifluoromethyl) sulfanyl] benzene
1 - chloro - 4 - [ (trifluoromethyl) sulfanyl] benzene, Chinese name or 1 - chloro - 4 - (trifluoromethyl) thio) benzene. The chemical properties of this substance are unique and have attracted much attention in the field of organic synthesis.
Looking at its structure, the chlorine atom and (trifluoromethyl thio) are respectively connected to the counterposition of the benzene ring. The chlorine atom has considerable activity and is prone to nucleophilic substitution reactions. In case of nucleophiles, the chlorine atom can be replaced, and then other functional groups can be introduced to expand the variety of compounds.
(trifluoromethylthio) has strong electron absorption, which connects to the benzene ring, changes the electron cloud density of the benzene ring, and affects the reactivity and selectivity of the benzene ring. Due to the existence of (trifluoromethylthio), the compound exhibits different properties from ordinary benzene derivatives in the aromatic electrophilic substitution reaction.
In terms of stability, the strong electronegativity of trifluoromethyl makes the molecular structure relatively stable. However, under specific conditions, such as high temperature, strong acid-base or strong oxidant environment, its structure may also change.
In addition, the physical properties of the compound, such as solubility and boiling point, are also affected by chlorine atoms and (trifluoromethylthio). In organic solvents, due to the hydrophobicity of (trifluoromethylthio), it has unique solubility in some organic solvents, which can be exploited in the process of separation and purification.
In short, 1-chloro-4 - (trifluoromethylthio) benzene has a special structure and rich chemical properties. It has potential application value in many fields such as organic synthesis and materials science. Chemists need to explore it in depth to understand more mysteries and uses.
Looking at its structure, the chlorine atom and (trifluoromethyl thio) are respectively connected to the counterposition of the benzene ring. The chlorine atom has considerable activity and is prone to nucleophilic substitution reactions. In case of nucleophiles, the chlorine atom can be replaced, and then other functional groups can be introduced to expand the variety of compounds.
(trifluoromethylthio) has strong electron absorption, which connects to the benzene ring, changes the electron cloud density of the benzene ring, and affects the reactivity and selectivity of the benzene ring. Due to the existence of (trifluoromethylthio), the compound exhibits different properties from ordinary benzene derivatives in the aromatic electrophilic substitution reaction.
In terms of stability, the strong electronegativity of trifluoromethyl makes the molecular structure relatively stable. However, under specific conditions, such as high temperature, strong acid-base or strong oxidant environment, its structure may also change.
In addition, the physical properties of the compound, such as solubility and boiling point, are also affected by chlorine atoms and (trifluoromethylthio). In organic solvents, due to the hydrophobicity of (trifluoromethylthio), it has unique solubility in some organic solvents, which can be exploited in the process of separation and purification.
In short, 1-chloro-4 - (trifluoromethylthio) benzene has a special structure and rich chemical properties. It has potential application value in many fields such as organic synthesis and materials science. Chemists need to explore it in depth to understand more mysteries and uses.
What are the preparation methods of 1-chloro-4- [ (trifluoromethyl) sulfanyl] benzene
1 - chloro - 4 - [ (trifluoromethyl) sulfanyl] benzene, the Chinese name is often 4 - (trifluoromethyl) chlorobenzene. There are many methods for its determination, which are described below.
One method can be obtained from the reverse reaction of 4-chlorothiophenol and trifluoromethylation. In the past, to obtain 4-chlorothiophenol, 4-chloroaniline was often used as the starting material. Shilling 4-chloroaniline diazotization, nitric acid and nitric acid were treated at low temperature to obtain diazonium. In addition, the diazonium group was set with thiocyanic acid to obtain 4-chlorophenyl thiocyanate. This ester is hydrolyzed to obtain 4-chlorothiophenol. The obtained 4-chlorothiophenol, then trifluoromethylated, such as trifluoromethyl sulfyl, can be obtained under the reversal of the reactive parts to obtain 1-chloro-4- [ (trifluoromethyl) sulfanyl] benzene. In the reversal, the reagent can promote the formation of thiophenol from 4-chlorothiophenol, which increases its nucleation and facilitates the reversal of trifluoromethylation.
Another method is to use 4-chlorobromobenzene as a starting material. First, 4-chlorobromobenzene is formed into Grignard, and 4-chlorobromobenzene is treated with chips and water ethyl ether to obtain 4-chlorophenyl bromide. In this reaction, the chemical compound 1-chloro-4 - [ (trifluoromethyl) sulfanyl] benzene can be obtained. In this reaction, the carbon-carbon of Grignard is nuclear, and it can be replaced by the sulfur-chloro-chloro-trifluoromethyl-chlorine.
Another method is to use the chemical reaction of 4-chlorophenylboronic acid containing trifluoromethyl sulfur group. This reaction needs to be carried out in the presence of catalytic catalysts, such as tetra (triphenylphosphine). In the reaction system, the reaction is also indispensable, which can promote the reaction. The boron atom of 4-chlorophenylboronic acid interacts to form boron atoms with nucleation, and the boron atoms containing trifluoromethyl sulfanyl react to form 1-chloro-4- [ (trifluoromethyl) sulfanyl] benzene.
Therefore, the above methods can be used for 1-chloro-4- [ (trifluoromethyl) sulfanyl] benzene. However, the availability of raw materials, the ease of reaction, and the high and low efficiency of each method are various factors, and they need to be used according to the needs of those who are good.
One method can be obtained from the reverse reaction of 4-chlorothiophenol and trifluoromethylation. In the past, to obtain 4-chlorothiophenol, 4-chloroaniline was often used as the starting material. Shilling 4-chloroaniline diazotization, nitric acid and nitric acid were treated at low temperature to obtain diazonium. In addition, the diazonium group was set with thiocyanic acid to obtain 4-chlorophenyl thiocyanate. This ester is hydrolyzed to obtain 4-chlorothiophenol. The obtained 4-chlorothiophenol, then trifluoromethylated, such as trifluoromethyl sulfyl, can be obtained under the reversal of the reactive parts to obtain 1-chloro-4- [ (trifluoromethyl) sulfanyl] benzene. In the reversal, the reagent can promote the formation of thiophenol from 4-chlorothiophenol, which increases its nucleation and facilitates the reversal of trifluoromethylation.
Another method is to use 4-chlorobromobenzene as a starting material. First, 4-chlorobromobenzene is formed into Grignard, and 4-chlorobromobenzene is treated with chips and water ethyl ether to obtain 4-chlorophenyl bromide. In this reaction, the chemical compound 1-chloro-4 - [ (trifluoromethyl) sulfanyl] benzene can be obtained. In this reaction, the carbon-carbon of Grignard is nuclear, and it can be replaced by the sulfur-chloro-chloro-trifluoromethyl-chlorine.
Another method is to use the chemical reaction of 4-chlorophenylboronic acid containing trifluoromethyl sulfur group. This reaction needs to be carried out in the presence of catalytic catalysts, such as tetra (triphenylphosphine). In the reaction system, the reaction is also indispensable, which can promote the reaction. The boron atom of 4-chlorophenylboronic acid interacts to form boron atoms with nucleation, and the boron atoms containing trifluoromethyl sulfanyl react to form 1-chloro-4- [ (trifluoromethyl) sulfanyl] benzene.
Therefore, the above methods can be used for 1-chloro-4- [ (trifluoromethyl) sulfanyl] benzene. However, the availability of raw materials, the ease of reaction, and the high and low efficiency of each method are various factors, and they need to be used according to the needs of those who are good.
Precautions for storing and transporting 1-chloro-4- [ (trifluoromethyl) sulfanyl] benzene
1-Chloro-4- [ (trifluoromethyl) thioalkyl] benzene is also an organic compound. When storing and transporting, it is necessary to pay attention to many matters.
The first concern is its chemical properties. This compound has a specific chemical activity and is easy to react with other substances. When storing, it should be kept away from oxidants, strong bases, strong acids, etc. If mixed with it, it may trigger violent chemical reactions and cause dangerous accidents, such as fire and explosion.
Furthermore, the storage environment is crucial. It should be placed in a cool, dry and well-ventilated place. If the temperature is too high, it may reduce the stability of the compound and accelerate its decomposition or deterioration; if the humidity is too high, it may cause reactions such as hydrolysis, which will damage its quality. And the storage place should be kept away from fire and heat sources to prevent danger caused by heat.
During transportation, the packaging must be solid and reliable. Appropriate packaging materials must be used to resist vibration, collision and friction, and to avoid material leakage caused by package damage. At the same time, the transportation vehicle should also be kept clean and free of other contaminants that may react with it.
In addition, relevant personnel must be familiar with its characteristics and hazards. Transportation and storage operators should be professionally trained and understand emergency response methods. In case of leakage and other accidents, it can be handled quickly and properly according to established procedures to minimize the harm.
In short, the whole process of storage and transportation of 1-chloro-4- [ (trifluoromethyl) thialkyl] benzene should be handled with caution and operated according to specifications to ensure safety.
The first concern is its chemical properties. This compound has a specific chemical activity and is easy to react with other substances. When storing, it should be kept away from oxidants, strong bases, strong acids, etc. If mixed with it, it may trigger violent chemical reactions and cause dangerous accidents, such as fire and explosion.
Furthermore, the storage environment is crucial. It should be placed in a cool, dry and well-ventilated place. If the temperature is too high, it may reduce the stability of the compound and accelerate its decomposition or deterioration; if the humidity is too high, it may cause reactions such as hydrolysis, which will damage its quality. And the storage place should be kept away from fire and heat sources to prevent danger caused by heat.
During transportation, the packaging must be solid and reliable. Appropriate packaging materials must be used to resist vibration, collision and friction, and to avoid material leakage caused by package damage. At the same time, the transportation vehicle should also be kept clean and free of other contaminants that may react with it.
In addition, relevant personnel must be familiar with its characteristics and hazards. Transportation and storage operators should be professionally trained and understand emergency response methods. In case of leakage and other accidents, it can be handled quickly and properly according to established procedures to minimize the harm.
In short, the whole process of storage and transportation of 1-chloro-4- [ (trifluoromethyl) thialkyl] benzene should be handled with caution and operated according to specifications to ensure safety.
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