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1-Chloro-4-[(Chloromethyl)Sulfanyl]Benzene
Linshang Chemical
|
HS Code |
843619 |
| Chemical Formula | C7H6Cl2S |
| Molar Mass | 193.09 g/mol |
| Appearance | Typically a colorless to light - colored liquid or solid |
| Boiling Point | Data may vary, but generally in a range related to its molecular structure |
| Melting Point | Also varies depending on purity and molecular packing |
| Density | Specific value depends on temperature and purity |
| Solubility In Water | Low solubility in water due to non - polar nature of the benzene ring and hydrophobic groups |
| Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, chloroform |
| Vapor Pressure | Relatively low vapor pressure at normal conditions |
| Flash Point | A value indicating flammability risk, data available in safety data sheets |
As an accredited 1-Chloro-4-[(Chloromethyl)Sulfanyl]Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1 - chloro - 4 - [(chloromethyl)sulfanyl]benzene: 500g in air - tight, corrosion - resistant bottles. |
| Storage | 1 - chloro - 4 - [(chloromethyl)sulfanyl]benzene should be stored in a cool, dry, well - ventilated area, away from heat sources and ignition points. It should be kept in a tightly - sealed container, preferably made of corrosion - resistant materials, to prevent leakage. Store it separately from oxidizing agents, strong acids, and bases to avoid potential chemical reactions. |
| Shipping | 1 - chloro - 4 - [(chloromethyl)sulfanyl]benzene is a chemical. It should be shipped in well - sealed, corrosion - resistant containers, following strict hazardous materials regulations, ensuring proper labeling for safe transportation. |
Competitive 1-Chloro-4-[(Chloromethyl)Sulfanyl]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.
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Where to Buy 1-Chloro-4-[(Chloromethyl)Sulfanyl]Benzene in China?
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As a leading 1-Chloro-4-[(Chloromethyl)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 are the chemical properties of 1-chloro-4- [ (chloromethyl) sulfanyl] benzene
1 - chloro - 4 - [ (chloromethyl) sulfanyl] benzene, this is an organic compound with unique chemical properties. Its appearance may be colorless to light yellow liquid with a special odor.
In terms of chemical activity, the groups connected to the chlorine atom and the sulfur atom are active check points. The chlorine atom in the chloromethyl group has nucleophilic substitution activity. Due to the strong polarity of the carbon-chlorine bond, it is vulnerable to the attack of nucleophilic reagents, causing the chlorine atom to be replaced. In case of hydroxyl negative ions, hydroxyl-containing compounds can be formed. This reaction is often used in organic synthesis to introduce new functional groups. The chlorine atom on the benzene ring also has a certain reactivity. Although its nucleophilic substitution reaction is slightly more difficult than that of the chlorine atom in the chloromethyl group, it can also be replaced under specific conditions, such as high temperature, strong base and the presence of catalysts. The chloromethyl group connected to the sulfur atom on the benzene ring changes the electron cloud density of the benzene ring due to the influence of the sulfur atom on the lone-to-electron, which affects the electrophilic substitution reaction activity of the benzene ring.
In addition, the sulfur atom in the compound can undergo oxidation reaction, and can be oxidized to sulfoxides or sulfones depending on the oxidation conditions. This oxidation reaction can be used to synthesize organosulfur compounds with
1 - chloro - 4 - [ (chloromethyl) sulfanyl] benzene is widely used in the field of organic synthesis due to its active functional group, and can be used as a key intermediate to prepare various organic compounds such as drugs, pesticides and materials.
In terms of chemical activity, the groups connected to the chlorine atom and the sulfur atom are active check points. The chlorine atom in the chloromethyl group has nucleophilic substitution activity. Due to the strong polarity of the carbon-chlorine bond, it is vulnerable to the attack of nucleophilic reagents, causing the chlorine atom to be replaced. In case of hydroxyl negative ions, hydroxyl-containing compounds can be formed. This reaction is often used in organic synthesis to introduce new functional groups. The chlorine atom on the benzene ring also has a certain reactivity. Although its nucleophilic substitution reaction is slightly more difficult than that of the chlorine atom in the chloromethyl group, it can also be replaced under specific conditions, such as high temperature, strong base and the presence of catalysts. The chloromethyl group connected to the sulfur atom on the benzene ring changes the electron cloud density of the benzene ring due to the influence of the sulfur atom on the lone-to-electron, which affects the electrophilic substitution reaction activity of the benzene ring.
In addition, the sulfur atom in the compound can undergo oxidation reaction, and can be oxidized to sulfoxides or sulfones depending on the oxidation conditions. This oxidation reaction can be used to synthesize organosulfur compounds with
1 - chloro - 4 - [ (chloromethyl) sulfanyl] benzene is widely used in the field of organic synthesis due to its active functional group, and can be used as a key intermediate to prepare various organic compounds such as drugs, pesticides and materials.
What are the main uses of 1-chloro-4- [ (chloromethyl) sulfanyl] benzene
1 - chloro - 4 - [ (chloromethyl) sulfanyl] benzene, Chinese name or 1 - chloro - 4 - (chloromethyl sulfanyl) benzene, this substance is widely used. In the field of organic synthesis, it is often used as a key intermediate. It can be combined with many reagents through a series of carefully designed chemical reactions to create more complex and unique organic compounds, such as some drug molecules with special biological activities or material monomers with excellent properties. It can be synthesized gradually by using this substance as a starting material.
In the field of materials science, it also shows important value. Due to the presence of chlorine atoms and sulfur methyl groups in the molecular structure, the substance is endowed with unique reactivity and chemical properties. Through appropriate polymerization or modification methods, it can be introduced into the structure of polymer materials, thereby significantly improving the physical and chemical properties of materials, such as enhancing the stability of materials, adjusting the solubility of materials, or imparting specific optical and electrical properties to materials.
In addition, in the field of fine chemicals, 1-chloro-4 - (chloromethylthio) benzene is often used to prepare various fine chemicals. For example, in the production process of some high-end coatings, inks, fragrances, and other products, this material can be used as a raw material through a specific reaction path to synthesize additives with specific properties and qualities, adding unique advantages and characteristics to fine chemical products to meet the stringent requirements of different industries for product performance.
In the field of materials science, it also shows important value. Due to the presence of chlorine atoms and sulfur methyl groups in the molecular structure, the substance is endowed with unique reactivity and chemical properties. Through appropriate polymerization or modification methods, it can be introduced into the structure of polymer materials, thereby significantly improving the physical and chemical properties of materials, such as enhancing the stability of materials, adjusting the solubility of materials, or imparting specific optical and electrical properties to materials.
In addition, in the field of fine chemicals, 1-chloro-4 - (chloromethylthio) benzene is often used to prepare various fine chemicals. For example, in the production process of some high-end coatings, inks, fragrances, and other products, this material can be used as a raw material through a specific reaction path to synthesize additives with specific properties and qualities, adding unique advantages and characteristics to fine chemical products to meet the stringent requirements of different industries for product performance.
What are the synthesis methods of 1-chloro-4- [ (chloromethyl) sulfanyl] benzene
1-Chloro-4- [ (chloromethyl) thio] benzene. To make it, there are various methods.
First, p-chlorothiophenol can be reacted with chloromethylation reagents. First take an appropriate amount of p-chlorothiophenol and place it in a clean reaction vessel. The device needs to be dry and airtight. Next, slowly add chloromethylation reagents, such as chloromethyl methyl ether. At the same time, add an appropriate amount of catalyst, such as anhydrous zinc chloride, to promote the reaction. During the reaction, it is necessary to strictly control the temperature. According to the characteristics of the reaction, it is often maintained in a specific temperature range, such as between 50 and 70 degrees Celsius, and constantly stirred to make the reactants fully contact. After a few hours, the reaction is completed, and the conventional separation and purification methods, such as extraction, distillation, recrystallization, etc., can obtain a pure product.
Second, p-chlorobenzyl chloride can also be used to react with vulcanization reagents. Prepare p-chlorobenzyl chloride first and place it in a suitable reaction device. Then, add a vulcanization reagent, such as an alcohol solution of sodium sulfide. The reaction should be carried out under mild conditions, with the temperature controlled at 30-50 degrees Celsius, and stirring to make the two fully functional. After the reaction is complete, after the separation and purification steps, the impurities can be removed to obtain 1-chloro-4- [ (chloromethyl) thio] benzene.
Or there are other methods, such as reacting with halogenated aromatics with sulfur-containing organometallic reagents. However, these methods may require special reaction conditions and reagents, and the operation may be more complicated, so the above two methods are more commonly used. When implemented, the appropriate one should be selected according to the actual situation, such as the availability of raw materials, cost, reaction equipment and other factors.
First, p-chlorothiophenol can be reacted with chloromethylation reagents. First take an appropriate amount of p-chlorothiophenol and place it in a clean reaction vessel. The device needs to be dry and airtight. Next, slowly add chloromethylation reagents, such as chloromethyl methyl ether. At the same time, add an appropriate amount of catalyst, such as anhydrous zinc chloride, to promote the reaction. During the reaction, it is necessary to strictly control the temperature. According to the characteristics of the reaction, it is often maintained in a specific temperature range, such as between 50 and 70 degrees Celsius, and constantly stirred to make the reactants fully contact. After a few hours, the reaction is completed, and the conventional separation and purification methods, such as extraction, distillation, recrystallization, etc., can obtain a pure product.
Second, p-chlorobenzyl chloride can also be used to react with vulcanization reagents. Prepare p-chlorobenzyl chloride first and place it in a suitable reaction device. Then, add a vulcanization reagent, such as an alcohol solution of sodium sulfide. The reaction should be carried out under mild conditions, with the temperature controlled at 30-50 degrees Celsius, and stirring to make the two fully functional. After the reaction is complete, after the separation and purification steps, the impurities can be removed to obtain 1-chloro-4- [ (chloromethyl) thio] benzene.
Or there are other methods, such as reacting with halogenated aromatics with sulfur-containing organometallic reagents. However, these methods may require special reaction conditions and reagents, and the operation may be more complicated, so the above two methods are more commonly used. When implemented, the appropriate one should be selected according to the actual situation, such as the availability of raw materials, cost, reaction equipment and other factors.
What to pay attention to when storing and transporting 1-chloro-4- [ (chloromethyl) sulfanyl] benzene
1-Chloro-4- [ (chloromethyl) thio] benzene, this is an organic compound, and more attention should be paid when storing and transporting.
First, because of its chemical activity, it must be stored in a cool, dry and well-ventilated place. Do not place in a high temperature or humid place to prevent chemical reactions. If the temperature is too high, or the volatilization of the substance is accelerated, not only will the content be damaged, but the volatile gaseous substance may be dangerous; humid environment may cause the substance to be damp, which in turn affects its purity and stability.
Second, this compound also requires packaging materials. Corrosive-resistant packaging, such as specific plastic materials or glass containers, should be used. Due to the chlorine content in this substance, it may have a corrosive effect on some metal materials, so it cannot be contained in ordinary metal containers, otherwise it may cause damage to the packaging and cause leakage.
Third, it should be isolated from other chemical substances during storage. Do not coexist with oxidizing agents, reducing agents and other easily reactive substances in the same room. Because its structure contains chloromethyl and sulfur groups, it may react violently with oxidizing agents or even cause explosions; in case of reducing agents or change its chemical structure, causing the substance to deteriorate.
Fourth, when transporting, be sure to ensure that the packaging is tightly sealed. Choose a safe mode of transportation to avoid bumps and collisions. If the packaging is damaged during transportation, the substance leaks, which not only pollutes the environment, but also poses a health threat to transporters. Due to its toxicity and irritation, accidental contact or inhalation can damage the human body.
In conclusion, when storing and transporting 1-chloro-4- [ (chloromethyl) thio] benzene, care must be taken from the environment, packaging, and operating practices to ensure safety.
First, because of its chemical activity, it must be stored in a cool, dry and well-ventilated place. Do not place in a high temperature or humid place to prevent chemical reactions. If the temperature is too high, or the volatilization of the substance is accelerated, not only will the content be damaged, but the volatile gaseous substance may be dangerous; humid environment may cause the substance to be damp, which in turn affects its purity and stability.
Second, this compound also requires packaging materials. Corrosive-resistant packaging, such as specific plastic materials or glass containers, should be used. Due to the chlorine content in this substance, it may have a corrosive effect on some metal materials, so it cannot be contained in ordinary metal containers, otherwise it may cause damage to the packaging and cause leakage.
Third, it should be isolated from other chemical substances during storage. Do not coexist with oxidizing agents, reducing agents and other easily reactive substances in the same room. Because its structure contains chloromethyl and sulfur groups, it may react violently with oxidizing agents or even cause explosions; in case of reducing agents or change its chemical structure, causing the substance to deteriorate.
Fourth, when transporting, be sure to ensure that the packaging is tightly sealed. Choose a safe mode of transportation to avoid bumps and collisions. If the packaging is damaged during transportation, the substance leaks, which not only pollutes the environment, but also poses a health threat to transporters. Due to its toxicity and irritation, accidental contact or inhalation can damage the human body.
In conclusion, when storing and transporting 1-chloro-4- [ (chloromethyl) thio] benzene, care must be taken from the environment, packaging, and operating practices to ensure safety.
What are the effects of 1-chloro-4- [ (chloromethyl) sulfanyl] benzene on the environment and human health?
1 - chloro - 4 - [ (chloromethyl) sulfanyl] benzene, this is an organic compound, commonly known as p-chlorobenzyl sulfur chloride. Looking at its structure, it contains chlorine atoms and sulfur-containing groups, and is active in nature. It is widely used in the field of chemical synthesis. However, this substance has certain effects on the environment and human health.
First talk about its impact on the environment. If this substance is released in the environment, it can interfere with the normal operation of the ecosystem due to the presence of chlorine and sulfur. In the soil, it may change the physical and chemical properties of the soil, hinder the absorption of nutrients by plant roots, affect plant growth and development, cause damage to vegetation, and destroy ecological balance. In the water body, it can deteriorate the water quality, poison aquatic organisms, affect the food chain of the aquatic ecosystem, and reduce biodiversity. And its chemical properties are stable, not easy to degrade, and will remain and accumulate in the environment for a long time, which will become more serious.
Re-discuss its impact on human health. Inhaled through the respiratory tract, this substance may irritate the mucosa of the respiratory tract, causing symptoms such as cough, asthma, and breathing difficulties. Long-term exposure may damage lung function and increase the risk of respiratory diseases. If exposed to the skin, it can cause skin allergies, redness, swelling, itching, and even burns. If ingested carelessly, it will damage the digestive system, cause nausea, vomiting, abdominal pain and other symptoms. In severe cases, it may affect the function of organs such as the liver and kidneys, threatening life and health. Due to its potential toxicity, when manufacturing and using this substance, it is necessary to strictly follow safety operating procedures and take protective measures to prevent damage to the environment and human body.
First talk about its impact on the environment. If this substance is released in the environment, it can interfere with the normal operation of the ecosystem due to the presence of chlorine and sulfur. In the soil, it may change the physical and chemical properties of the soil, hinder the absorption of nutrients by plant roots, affect plant growth and development, cause damage to vegetation, and destroy ecological balance. In the water body, it can deteriorate the water quality, poison aquatic organisms, affect the food chain of the aquatic ecosystem, and reduce biodiversity. And its chemical properties are stable, not easy to degrade, and will remain and accumulate in the environment for a long time, which will become more serious.
Re-discuss its impact on human health. Inhaled through the respiratory tract, this substance may irritate the mucosa of the respiratory tract, causing symptoms such as cough, asthma, and breathing difficulties. Long-term exposure may damage lung function and increase the risk of respiratory diseases. If exposed to the skin, it can cause skin allergies, redness, swelling, itching, and even burns. If ingested carelessly, it will damage the digestive system, cause nausea, vomiting, abdominal pain and other symptoms. In severe cases, it may affect the function of organs such as the liver and kidneys, threatening life and health. Due to its potential toxicity, when manufacturing and using this substance, it is necessary to strictly follow safety operating procedures and take protective measures to prevent damage to the environment and human body.
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