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(4-Chlorobenzenesulphonyl)Acetone
Linshang Chemical
|
HS Code |
362381 |
| Chemical Formula | C9H9ClO3S |
| Molar Mass | 232.684 g/mol |
| Appearance | Typically a solid (physical state can vary based on conditions) |
| Melting Point | Specific value would require further research |
| Boiling Point | Specific value would require further research |
| Solubility In Water | Expected to be low, as it is an organic compound with a relatively non - polar benzene ring |
| Solubility In Organic Solvents | Likely soluble in common organic solvents like dichloromethane, ethyl acetate |
| Density | Specific value would require further research |
| Stability | Can be stable under normal conditions, but may react with strong oxidizing or reducing agents |
As an accredited (4-Chlorobenzenesulphonyl)Acetone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of (4 - chlorobenzenesulphonyl)acetone packaged in air - tight plastic containers. |
| Storage | (4 - chlorobenzenesulphonyl)acetone should be stored in a cool, dry, well - ventilated area, away from heat sources and open flames. Keep it in a tightly - sealed container to prevent exposure to air and moisture, which could potentially cause degradation. Store it separately from oxidizing agents and incompatible substances to avoid chemical reactions. |
| Shipping | (4 - chlorobenzenesulphonyl)acetone is shipped in properly sealed, corrosion - resistant containers. It adheres to strict chemical shipping regulations, ensuring safe transport to prevent leakage and maintain its integrity during transit. |
Competitive (4-Chlorobenzenesulphonyl)Acetone 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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Tel: +8615365006308
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Where to Buy (4-Chlorobenzenesulphonyl)Acetone in China?
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As a leading (4-Chlorobenzenesulphonyl)Acetone supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
(4-chlorobenzenesulphonyl) What is the main use of acetone?
(4-Chlorobenzenesulfonyl) acetone has a wide range of uses. In the field of organic synthesis, it is often a key intermediate.
First, it can be used to create drugs with specific structures. Due to the unique chemical structure of this compound, it can be used to build the molecular framework required for drug activity through organic reactions. For example, it may participate in the construction of heterocyclic structures containing specific functional groups. This heterocyclic structure is the core pharmacodynamic group in many drugs, which helps the drug to precisely bind to biological targets, and then exhibit pharmacological activity.
Second, it is also used in the field of materials science. It can be chemically modified and introduced into polymer materials to change the physical and chemical properties of the material. Such as enhancing the stability of the material, adjusting the hydrophilicity of the material surface, etc. This is because the sulfonyl group of (4-chlorobenzenesulfonyl) acetone and the chlorine atom and other functional groups can chemically react with the polymer chain to form covalent bonds or other interactions, thereby improving the overall properties of the material.
Furthermore, in the preparation of fine chemicals, it is also an important raw material. Surfactants and catalyst ligands with special properties can be prepared. Surfactants can be oriented at the solution interface by virtue of their structural characteristics, reduce surface tension, and exhibit good emulsification and dispersion properties; while catalyst ligands can coordinate with metal ions, regulate catalyst activity and selectivity, and play a key role in catalytic reactions.
In summary, (4-chlorobenzenesulfonyl) acetone, with its unique structure, has important uses in drug synthesis, materials science, fine chemical preparation, and other fields, promoting technological development and innovation in various fields.
First, it can be used to create drugs with specific structures. Due to the unique chemical structure of this compound, it can be used to build the molecular framework required for drug activity through organic reactions. For example, it may participate in the construction of heterocyclic structures containing specific functional groups. This heterocyclic structure is the core pharmacodynamic group in many drugs, which helps the drug to precisely bind to biological targets, and then exhibit pharmacological activity.
Second, it is also used in the field of materials science. It can be chemically modified and introduced into polymer materials to change the physical and chemical properties of the material. Such as enhancing the stability of the material, adjusting the hydrophilicity of the material surface, etc. This is because the sulfonyl group of (4-chlorobenzenesulfonyl) acetone and the chlorine atom and other functional groups can chemically react with the polymer chain to form covalent bonds or other interactions, thereby improving the overall properties of the material.
Furthermore, in the preparation of fine chemicals, it is also an important raw material. Surfactants and catalyst ligands with special properties can be prepared. Surfactants can be oriented at the solution interface by virtue of their structural characteristics, reduce surface tension, and exhibit good emulsification and dispersion properties; while catalyst ligands can coordinate with metal ions, regulate catalyst activity and selectivity, and play a key role in catalytic reactions.
In summary, (4-chlorobenzenesulfonyl) acetone, with its unique structure, has important uses in drug synthesis, materials science, fine chemical preparation, and other fields, promoting technological development and innovation in various fields.
(4-chlorobenzenesulphonyl) What are the physical properties of acetone
(4-Chlorobenzenesulfonyl) acetone is also an organic compound. Its physical properties are quite elusive.
Looking at its properties, it may be in a solid state at room temperature, but it also depends on the surrounding conditions. If the temperature is slightly higher, it may appear to soften; if the temperature decreases, it may be in a firmer state. Its color is often close to colorless to slightly yellow, and the texture is more delicate.
When it comes to odor, (4-chlorobenzenesulfonyl) acetone may emit a specific smell, but it is not pungent and intolerable. It is a unique organic smell that can be smelled for a long time, or its special taste can be distinguished.
In terms of solubility, it often has a certain solubility in organic solvents, such as ethanol, ether, etc. This is due to the interaction between organic solvents and (4-chlorobenzenesulfonyl) acetone molecules, so that it can be dispersed in the solvent system. In water, its solubility is relatively limited, due to the characteristics of its molecular structure, the force between water molecules and water molecules is weak.
Its melting point and boiling point are also important physical properties. The determination of the melting point can help to determine the critical temperature of its solid state to liquid state. The boiling point is related to the conditions for its liquid state to gas state. After experimental investigation, the specific values of its melting point and boiling point can be known, which are crucial for the separation, purification and application of this compound.
Density is also a consideration. The density of (4-chlorobenzenesulfonyl) acetone may be different from that of water, and this property has a significant impact in some experiments and industrial processes involving phase separation or mixing.
The physical properties of this compound are interrelated and affect its application in various fields, which is the key to the study of organic chemistry.
Looking at its properties, it may be in a solid state at room temperature, but it also depends on the surrounding conditions. If the temperature is slightly higher, it may appear to soften; if the temperature decreases, it may be in a firmer state. Its color is often close to colorless to slightly yellow, and the texture is more delicate.
When it comes to odor, (4-chlorobenzenesulfonyl) acetone may emit a specific smell, but it is not pungent and intolerable. It is a unique organic smell that can be smelled for a long time, or its special taste can be distinguished.
In terms of solubility, it often has a certain solubility in organic solvents, such as ethanol, ether, etc. This is due to the interaction between organic solvents and (4-chlorobenzenesulfonyl) acetone molecules, so that it can be dispersed in the solvent system. In water, its solubility is relatively limited, due to the characteristics of its molecular structure, the force between water molecules and water molecules is weak.
Its melting point and boiling point are also important physical properties. The determination of the melting point can help to determine the critical temperature of its solid state to liquid state. The boiling point is related to the conditions for its liquid state to gas state. After experimental investigation, the specific values of its melting point and boiling point can be known, which are crucial for the separation, purification and application of this compound.
Density is also a consideration. The density of (4-chlorobenzenesulfonyl) acetone may be different from that of water, and this property has a significant impact in some experiments and industrial processes involving phase separation or mixing.
The physical properties of this compound are interrelated and affect its application in various fields, which is the key to the study of organic chemistry.
(4-chlorobenzenesulphonyl) What are the chemical properties of acetone
(4-Chlorobenzenesulfonyl) acetone is one of the organic compounds. Its chemical properties are unique and valuable for investigation.
From the structural point of view, (4-chlorobenzenesulfonyl) acetone contains benzene rings, chlorine atoms, sulfonyl groups and acetone structural fragments. This structure endows it with various characteristics.
In terms of reactivity, benzene rings are aromatic. Although they are relatively stable, under certain conditions, electrophilic substitution reactions can occur. Because chlorine atoms and sulfonyl groups are electron-withdrawing groups, the electron cloud density of benzene rings will decrease, and the electrophilic substitution reactivity will decrease slightly, and new substituents are more likely to enter the meso. In the
sulfonyl group, the sulfur atom is in a high valence state and has certain oxidation properties, which can participate in redox-related reactions. At the same time, the existence of sulfonyl groups enhances the polarity of molecules and affects their solubility and other physical properties, making them more soluble in polar solvents or better than non-polar solvents. The carbonyl group of the structural part of acetone is the reactive center, and many typical reactions can occur. For example, nucleophilic addition reactions, because the carbon-oxygen double bond electron cloud in the carbonyl group is biased towards the oxygen atom, the carbon atom is partially positively charged and vulnerable to attack by nucleophilic reagents. Common nucleophilic reagents such as alcohols and amines can react with them to generate corresponding addition products.
In addition, the α-hydrogen atom of (4-chlorobenzenesulfonyl) acetone is acidic due to the double electron-withdrawing effect of carbonyl and sulfonyl, and it is easy to leave under the action of alkali, which in turn triggers subsequent reactions, such as participating in condensation reactions. It can be used as a key intermediate in the field of organic synthesis to construct more complex organic molecular structures.
From the structural point of view, (4-chlorobenzenesulfonyl) acetone contains benzene rings, chlorine atoms, sulfonyl groups and acetone structural fragments. This structure endows it with various characteristics.
In terms of reactivity, benzene rings are aromatic. Although they are relatively stable, under certain conditions, electrophilic substitution reactions can occur. Because chlorine atoms and sulfonyl groups are electron-withdrawing groups, the electron cloud density of benzene rings will decrease, and the electrophilic substitution reactivity will decrease slightly, and new substituents are more likely to enter the meso. In the
sulfonyl group, the sulfur atom is in a high valence state and has certain oxidation properties, which can participate in redox-related reactions. At the same time, the existence of sulfonyl groups enhances the polarity of molecules and affects their solubility and other physical properties, making them more soluble in polar solvents or better than non-polar solvents. The carbonyl group of the structural part of acetone is the reactive center, and many typical reactions can occur. For example, nucleophilic addition reactions, because the carbon-oxygen double bond electron cloud in the carbonyl group is biased towards the oxygen atom, the carbon atom is partially positively charged and vulnerable to attack by nucleophilic reagents. Common nucleophilic reagents such as alcohols and amines can react with them to generate corresponding addition products.
In addition, the α-hydrogen atom of (4-chlorobenzenesulfonyl) acetone is acidic due to the double electron-withdrawing effect of carbonyl and sulfonyl, and it is easy to leave under the action of alkali, which in turn triggers subsequent reactions, such as participating in condensation reactions. It can be used as a key intermediate in the field of organic synthesis to construct more complex organic molecular structures.
(4-chlorobenzenesulphonyl) What is the synthesis method of acetone?
The method of making (4-chlorobenzenesulfonyl) acetone is not detailed in the ancient book "Tiangongkai", but it can be inferred according to the chemical process thinking contained in it.
To make this product, you need to prepare 4-chlorobenzenesulfonyl chloride and acetone as raw materials. Both are key to synthesis. In a suitable reaction vessel, using a base as a catalyst can promote the reaction of the two. The choice of base should be a mild and effective catalyst, such as potassium carbonate.
Set the reactor in a suitable temperature environment, about room temperature to 50 degrees Celsius, and stir slowly. Due to high temperature, side reactions may occur, and if it is too low, the reaction will be slow. When stirring, the materials are uniformly mixed and the reaction proceeds in an orderly manner. The sulfonyl group of 4-chlorobenzenesulfonyl chloride undergoes a nucleophilic substitution reaction with the active hydrogen of the carbonyl ortho-position of acetone.
After the reaction is completed, the product is mixed in the reaction system. To obtain pure (4-chlorobenzenesulfonyl) acetone, it needs to go through the steps of separation and purification. First, it is extracted with an organic solvent to enrich the product in the organic phase. Then, the organic solvent and the unreacted raw material are removed by distillation according to the difference in boiling points of each component. After recrystallization, a suitable solvent is selected to crystallize and precipitate the product, thereby obtaining pure (4-chlorobenzenesulfonyl) acetone. In this way, the synthesis of this substance can be achieved by following the basic principles of chemistry and operating techniques, as well as antique thinking.
To make this product, you need to prepare 4-chlorobenzenesulfonyl chloride and acetone as raw materials. Both are key to synthesis. In a suitable reaction vessel, using a base as a catalyst can promote the reaction of the two. The choice of base should be a mild and effective catalyst, such as potassium carbonate.
Set the reactor in a suitable temperature environment, about room temperature to 50 degrees Celsius, and stir slowly. Due to high temperature, side reactions may occur, and if it is too low, the reaction will be slow. When stirring, the materials are uniformly mixed and the reaction proceeds in an orderly manner. The sulfonyl group of 4-chlorobenzenesulfonyl chloride undergoes a nucleophilic substitution reaction with the active hydrogen of the carbonyl ortho-position of acetone.
After the reaction is completed, the product is mixed in the reaction system. To obtain pure (4-chlorobenzenesulfonyl) acetone, it needs to go through the steps of separation and purification. First, it is extracted with an organic solvent to enrich the product in the organic phase. Then, the organic solvent and the unreacted raw material are removed by distillation according to the difference in boiling points of each component. After recrystallization, a suitable solvent is selected to crystallize and precipitate the product, thereby obtaining pure (4-chlorobenzenesulfonyl) acetone. In this way, the synthesis of this substance can be achieved by following the basic principles of chemistry and operating techniques, as well as antique thinking.
(4-chlorobenzenesulphonyl) What are the precautions in the storage and transportation of acetone
(4-Chlorobenzenesulfonyl) acetone is an organic compound. When storing and transporting, many things need to be paid attention to.
First, when storing, it must be cool, dry and well ventilated. Because it may be more sensitive to heat, high temperature is easy to cause it to deteriorate, so it should be kept away from heat sources and fire sources. If it is placed in a humid environment, or causes chemical reactions such as hydrolysis, which damages its quality, it is essential to dry it in an environment.
Second, it needs to be stored separately from oxidants, acids, alkalis and other substances. This compound is chemically active and may come into contact with oxidants, or risk violent reactions, or even cause combustion and explosion. Contact with acids and alkalis may also cause chemical reactions, changing its chemical structure and properties.
Third, during transportation, ensure that the packaging is complete and well sealed. To prevent leakage, it will cause harm to the environment and transportation personnel. And the means of transportation should be clean and dry to avoid mixing impurities and affecting their quality. At the same time, the transportation should follow the relevant regulations on the transportation of hazardous chemicals, and be equipped with necessary emergency treatment equipment and protective equipment. If there is an accident such as leakage on the way, it can be properly disposed of in time to reduce the harm.
Fourth, whether it is storage or transportation, it is necessary to make a good mark. Clearly mark its name, nature, dangerous characteristics and other information to facilitate the identification and operation of relevant personnel, and avoid safety accidents caused by misoperation. Only by strictly following the above points can we ensure the safety and quality of (4-chlorobenzenesulfonyl) acetone during storage and transportation.
First, when storing, it must be cool, dry and well ventilated. Because it may be more sensitive to heat, high temperature is easy to cause it to deteriorate, so it should be kept away from heat sources and fire sources. If it is placed in a humid environment, or causes chemical reactions such as hydrolysis, which damages its quality, it is essential to dry it in an environment.
Second, it needs to be stored separately from oxidants, acids, alkalis and other substances. This compound is chemically active and may come into contact with oxidants, or risk violent reactions, or even cause combustion and explosion. Contact with acids and alkalis may also cause chemical reactions, changing its chemical structure and properties.
Third, during transportation, ensure that the packaging is complete and well sealed. To prevent leakage, it will cause harm to the environment and transportation personnel. And the means of transportation should be clean and dry to avoid mixing impurities and affecting their quality. At the same time, the transportation should follow the relevant regulations on the transportation of hazardous chemicals, and be equipped with necessary emergency treatment equipment and protective equipment. If there is an accident such as leakage on the way, it can be properly disposed of in time to reduce the harm.
Fourth, whether it is storage or transportation, it is necessary to make a good mark. Clearly mark its name, nature, dangerous characteristics and other information to facilitate the identification and operation of relevant personnel, and avoid safety accidents caused by misoperation. Only by strictly following the above points can we ensure the safety and quality of (4-chlorobenzenesulfonyl) acetone during storage and transportation.
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