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Benzene, ((Chloromethyl)Sulfonyl)-
Linshang Chemical
|
HS Code |
894076 |
| Chemical Formula | C7H7ClO2S |
| Molar Mass | 190.647 g/mol |
| Solubility In Water | Limited solubility expected as it has non - polar benzene ring and polar sulfonyl - chloromethyl group |
| Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, toluene due to non - polar benzene part |
| Vapor Pressure | Low vapor pressure expected considering polar groups and relatively high molar mass |
As an accredited Benzene, ((Chloromethyl)Sulfonyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of “Benzene, ((chloromethyl)sulfonyl)-” in a sealed, chemical - resistant container. |
| Storage | **Storage of [(Chloromethyl)sulfonyl] - benzene**: Store this chemical in a cool, dry, well - ventilated area away from heat, flames, and ignition sources. Keep it in a tightly sealed container to prevent leakage. As it may be reactive and potentially hazardous, segregate it from incompatible substances such as oxidizing agents, bases, and reducing agents. Ensure storage areas comply with safety regulations. |
| Shipping | Benzene, ((chloromethyl)sulfonyl)- is a chemical that requires careful shipping. It should be transported in properly labeled, sealed containers compliant with hazardous material regulations to prevent spills and ensure safety during transit. |
Competitive Benzene, ((Chloromethyl)Sulfonyl)- prices that fit your budget—flexible terms and customized quotes for every order.
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Benzene, ((chloromethyl) sulfonyl) - what is the chemical structure?
Benzene, (chloromethyl) sulfonyl) - The chemical structure of this compound is really an interesting topic in the field of organic chemistry. Its structure is based on the benzene ring, which is a typical structure of aromatic hydrocarbons, with unique stability and electron conjugation system. On the benzene ring, the functional group of (chloromethyl) sulfonyl is connected.
(chloromethyl) sulfonyl In the sulfonyl group, chloromethyl-CH ² Cl, the chlorine atom is covalently bonded to methylene-CH ² -, and the methylene is in turn connected to sulfonyl-SO 2O -. In the sulfonyl group, the sulfur atom forms a double bond with two oxygen atoms, showing a specific electron cloud distribution and chemical activity.
This combination of structures endows this compound with unique physical and chemical properties. The chloromethyl part, due to the electronegativity of the chlorine atom, has a certain electrophilicity and can participate in a variety of nucleophilic substitution reactions. The sulfonyl group affects the polarity and reactivity of the molecule, and its strong electron absorption affects the electron cloud density of the benzene ring, which in turn changes the substitution reaction check point and activity on the benzene ring. The chemical structure of this compound is like a carefully constructed microscopic chemical castle, and the cooperation of each part determines its unique performance on the chemical reaction stage.
(chloromethyl) sulfonyl In the sulfonyl group, chloromethyl-CH ² Cl, the chlorine atom is covalently bonded to methylene-CH ² -, and the methylene is in turn connected to sulfonyl-SO 2O -. In the sulfonyl group, the sulfur atom forms a double bond with two oxygen atoms, showing a specific electron cloud distribution and chemical activity.
This combination of structures endows this compound with unique physical and chemical properties. The chloromethyl part, due to the electronegativity of the chlorine atom, has a certain electrophilicity and can participate in a variety of nucleophilic substitution reactions. The sulfonyl group affects the polarity and reactivity of the molecule, and its strong electron absorption affects the electron cloud density of the benzene ring, which in turn changes the substitution reaction check point and activity on the benzene ring. The chemical structure of this compound is like a carefully constructed microscopic chemical castle, and the cooperation of each part determines its unique performance on the chemical reaction stage.
Benzene, ((chloromethyl) sulfonyl) - What are the physical properties?
(Chloromethyl) sulfonylbenzene is a kind of organic compound. It has various physical properties, which are described in detail by you today.
Looking at its properties, under normal circumstances, (chloromethyl) sulfonylbenzene is mostly colorless to slightly yellow liquid, with a clear texture and light transmission. Looking at it, it can be seen that it is uniform and free of impurities. The smell of its odor is slightly irritating, but it is not extremely strong, and it is slightly uncomfortable to smell, but it is not unbearable.
When it comes to the melting point, the melting point of this compound is about [X] ° C. Under this specific temperature, it gradually melts from a solid state to a liquid state. The change of morphology is due to the change of intermolecular forces caused by temperature. The boiling point is about [X] ° C. At this high temperature, the liquid then turns into a gaseous state, and the molecular motion intensifies, breaking free from the liquid phase.
In terms of solubility, (chloromethyl) sulfonyl benzene can be dissolved in organic solvents, such as common ether and dichloromethane, etc., and the two can be mixed to form a uniform solution. However, in water, its solubility is not good. Due to the characteristics of its molecular structure, it is difficult to form an effective interaction with water molecules, so it is difficult to dissolve in water.
In terms of density, its density is higher than that of water. If it is placed in a container with water, it can be seen that it sinks underwater and is clearly layered. This varies depending on the density.
In addition, the volatility of (chloromethyl) sulfonylbenzene is relatively moderate, and it is not as volatile as some low-boiling substances, nor is it difficult to evaporate at high boiling point. In the environment of room temperature and pressure, it evaporates slowly, and the existence of its smell can be gradually felt in the air. These physical properties are determined by the structure and composition of its molecules, which have a key impact on its application in chemical industry, scientific research and other fields.
Looking at its properties, under normal circumstances, (chloromethyl) sulfonylbenzene is mostly colorless to slightly yellow liquid, with a clear texture and light transmission. Looking at it, it can be seen that it is uniform and free of impurities. The smell of its odor is slightly irritating, but it is not extremely strong, and it is slightly uncomfortable to smell, but it is not unbearable.
When it comes to the melting point, the melting point of this compound is about [X] ° C. Under this specific temperature, it gradually melts from a solid state to a liquid state. The change of morphology is due to the change of intermolecular forces caused by temperature. The boiling point is about [X] ° C. At this high temperature, the liquid then turns into a gaseous state, and the molecular motion intensifies, breaking free from the liquid phase.
In terms of solubility, (chloromethyl) sulfonyl benzene can be dissolved in organic solvents, such as common ether and dichloromethane, etc., and the two can be mixed to form a uniform solution. However, in water, its solubility is not good. Due to the characteristics of its molecular structure, it is difficult to form an effective interaction with water molecules, so it is difficult to dissolve in water.
In terms of density, its density is higher than that of water. If it is placed in a container with water, it can be seen that it sinks underwater and is clearly layered. This varies depending on the density.
In addition, the volatility of (chloromethyl) sulfonylbenzene is relatively moderate, and it is not as volatile as some low-boiling substances, nor is it difficult to evaporate at high boiling point. In the environment of room temperature and pressure, it evaporates slowly, and the existence of its smell can be gradually felt in the air. These physical properties are determined by the structure and composition of its molecules, which have a key impact on its application in chemical industry, scientific research and other fields.
Benzene, ((chloromethyl) sulfonyl) - What are the common uses?
Benzene, (chloromethyl) sulfonyl) is a key substance for common use. In the field of chemical industry, it is an important raw material for organic synthesis. It can be used to prepare various fine chemicals through specific processes.
First, in the synthesis of medicine, it can be used as an intermediate to participate in the construction of many drug molecules. Because of its unique structure, it can impart specific activities and properties to drugs, helping to create good drugs for treating various diseases.
Second, in the field of materials science, it can be used to synthesize special polymer materials. By chemical reaction, it can be integrated into the polymer skeleton, which can make the material have excellent properties such as chemical resistance and high mechanical strength. It has great potential in high-end fields such as aerospace and electronic devices.
Furthermore, it also has a place in the manufacture of pesticides. Using it as a starting material, through a series of transformations, efficient and low-toxicity pesticides can be prepared, providing strong support for agricultural pest control.
Synthesis method is often selected according to different needs and conditions. Or introduce chloromethyl through halogenation reaction, and then add sulfonyl group through sulfonylation step. When operating, be sure to pay attention to the precise control of reaction conditions, such as temperature, pressure, catalyst dosage, etc., all of which are related to the purity and yield of the product. At the same time, safety protection should not be underestimated, because some raw materials and products may be toxic and corrosive, and must be operated in accordance with regulations to prevent harm to people and the environment.
First, in the synthesis of medicine, it can be used as an intermediate to participate in the construction of many drug molecules. Because of its unique structure, it can impart specific activities and properties to drugs, helping to create good drugs for treating various diseases.
Second, in the field of materials science, it can be used to synthesize special polymer materials. By chemical reaction, it can be integrated into the polymer skeleton, which can make the material have excellent properties such as chemical resistance and high mechanical strength. It has great potential in high-end fields such as aerospace and electronic devices.
Furthermore, it also has a place in the manufacture of pesticides. Using it as a starting material, through a series of transformations, efficient and low-toxicity pesticides can be prepared, providing strong support for agricultural pest control.
Synthesis method is often selected according to different needs and conditions. Or introduce chloromethyl through halogenation reaction, and then add sulfonyl group through sulfonylation step. When operating, be sure to pay attention to the precise control of reaction conditions, such as temperature, pressure, catalyst dosage, etc., all of which are related to the purity and yield of the product. At the same time, safety protection should not be underestimated, because some raw materials and products may be toxic and corrosive, and must be operated in accordance with regulations to prevent harm to people and the environment.
Benzene, ((chloromethyl) sulfonyl) - What are the preparation methods?
The method of preparing (chloromethyl) sulfonyl) -benzene has been studied in the past. One method can be obtained by electrophilic substitution reaction between benzene and (chloromethyl) sulfonyl chloride under suitable conditions with the help of a catalyst. Among them, the catalyst is often selected as an anhydrous aluminum trichloride and other Lewis acids, which can polarize (chloromethyl) sulfonyl chloride and make it easier to react with benzene. During the reaction, the benzene and the catalyst are placed in the reaction vessel, and the (chloromethyl) sulfonyl chloride is slowly added dropwise, and the temperature is controlled and stirred to make the reaction proceed smoothly.
There is another method. The corresponding intermediate is first prepared from benzene, and then the (chloromethyl) sulfonyl group is introduced through a series of conversions If benzene is first formed into a derivative containing an active group, then the derivative reacts with a reagent containing (chloromethyl) sulfonyl group, and goes through many steps such as substitution and addition, and finally obtains the target product.
During the preparation process, it is crucial to control the conditions. If the temperature is too high, it is easy to produce side reactions and cause the product to be impure; if the temperature is too low, the reaction will be delayed and take a long time. And the ratio of reactants, reaction time and other factors have a significant impact on the yield and purity of the product. Therefore, it is necessary to fine-tune various conditions to achieve the best conditions and obtain high-purity ((chloromethyl) sulfonyl) -benzene.
There is another method. The corresponding intermediate is first prepared from benzene, and then the (chloromethyl) sulfonyl group is introduced through a series of conversions If benzene is first formed into a derivative containing an active group, then the derivative reacts with a reagent containing (chloromethyl) sulfonyl group, and goes through many steps such as substitution and addition, and finally obtains the target product.
During the preparation process, it is crucial to control the conditions. If the temperature is too high, it is easy to produce side reactions and cause the product to be impure; if the temperature is too low, the reaction will be delayed and take a long time. And the ratio of reactants, reaction time and other factors have a significant impact on the yield and purity of the product. Therefore, it is necessary to fine-tune various conditions to achieve the best conditions and obtain high-purity ((chloromethyl) sulfonyl) -benzene.
Benzene, ((chloromethyl) sulfonyl) - What are the characteristics of chemical reactions?
"Tiangong Kaiwu" is simple and concise, and the answer in classical Chinese form is as follows:
Fubenzene ((chloromethyl) sulfonyl) is quite unique in chemical reactions. First, its structure contains chloromethyl and sulfonyl groups in the benzene ring, which gives it special reactivity. Chloromethyl chloride atoms are active and prone to nucleophilic substitution. In case of nucleophilic reagents, chlorine atoms can be replaced, new groups are introduced, and the reaction path is expanded.
Second, the sulfonyl group has strong electron absorption, which affects the distribution of benzene ring electron cloud, reduces the density of benzene ring electron cloud, changes the activity of benzene ring electrophilic substitution reaction, and the density of the adjacent and para-position electron cloud is slightly higher, so the electrophilic substitution is mostly in the adjacent and para-position.
Third, the stability of this substance also has characteristics. Although the benzene ring has a certain stability, the presence of chloromethyl and sulfonyl groups disturbs the overall stability. Under specific conditions, such as high temperature, strong acid-base environment, intra-molecular chemical bonds or rearrangement, fracture, complex reactions occur. Fourth, in terms of solubility, the benzene ring has a hydrophobic structure, and the sulfonyl group has a certain polarity, causing it to exhibit a special law of solubility in organic solvents and water. It may have a certain solubility in polar organic solvents, but it has poor solubility in water. This property also affects the environment and manner in which it participates in the reaction.
Fubenzene ((chloromethyl) sulfonyl) is quite unique in chemical reactions. First, its structure contains chloromethyl and sulfonyl groups in the benzene ring, which gives it special reactivity. Chloromethyl chloride atoms are active and prone to nucleophilic substitution. In case of nucleophilic reagents, chlorine atoms can be replaced, new groups are introduced, and the reaction path is expanded.
Second, the sulfonyl group has strong electron absorption, which affects the distribution of benzene ring electron cloud, reduces the density of benzene ring electron cloud, changes the activity of benzene ring electrophilic substitution reaction, and the density of the adjacent and para-position electron cloud is slightly higher, so the electrophilic substitution is mostly in the adjacent and para-position.
Third, the stability of this substance also has characteristics. Although the benzene ring has a certain stability, the presence of chloromethyl and sulfonyl groups disturbs the overall stability. Under specific conditions, such as high temperature, strong acid-base environment, intra-molecular chemical bonds or rearrangement, fracture, complex reactions occur. Fourth, in terms of solubility, the benzene ring has a hydrophobic structure, and the sulfonyl group has a certain polarity, causing it to exhibit a special law of solubility in organic solvents and water. It may have a certain solubility in polar organic solvents, but it has poor solubility in water. This property also affects the environment and manner in which it participates in the reaction.
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