Linshang Chemical
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N-Chloro-N-Cyclohexylbenzenesulfonamide
Linshang Chemical
|
HS Code |
215228 |
| Chemical Formula | C12H16ClNO2S |
| Molecular Weight | 273.78 |
| Appearance | Solid |
| Color | Typically white or off - white |
| Odor | May have a characteristic odor |
| Melting Point | Specific value would require literature search |
| Boiling Point | Specific value would require literature search |
| Solubility In Water | Low solubility |
| Solubility In Organic Solvents | Soluble in some organic solvents like dichloromethane |
| Stability | Stable under normal conditions, may decompose under extreme heat or in presence of strong reactants |
| Hazard Class | May be classified as an irritant, details need literature check |
| Flash Point | Specific value would require literature search |
As an accredited N-Chloro-N-Cyclohexylbenzenesulfonamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1 kg of N - chloro - n - cyclohexylbenzenesulfonamide in a sealed plastic bag. |
| Storage | N - chloro - n - cyclohexylbenzenesulfonamide should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and incompatible substances such as strong acids, bases, and reducing agents. Store in a tightly - sealed container to prevent moisture absorption and potential degradation, ensuring its stability during storage. |
| Shipping | N - chloro - n - cyclohexylbenzenesulfonamide, a chemical, is shipped in accordance with strict hazardous materials regulations. Packed in suitable containers to prevent leakage, it's transported by approved carriers ensuring safety during transit. |
Competitive N-Chloro-N-Cyclohexylbenzenesulfonamide prices that fit your budget—flexible terms and customized quotes for every order.
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What are the main uses of N-chloro-n-cyclohexylbenzenesulfonamide?
N-chloro-N-cyclohexylbenzenesulfonamide has a wide range of uses in the field of chemical medicine. Its primary use is as a chlorination reagent in organic synthesis.
In organic synthesis, this compound is often used as a chlorination agent to introduce chlorine atoms into organic molecules. Due to its structural characteristics, it can provide an active chlorine source and participate in a variety of chemical reactions. For example, under specific reaction conditions, it can selectively chlorinate hydrogen at the allyl or benzyl sites. This chlorination reaction has high regioselectivity and chemical selectivity, which can accurately achieve the construction of target molecules. When synthesizing complex organic compounds, it is a key step to help chemists obtain the desired structure to meet the needs of specific structural compounds in the fields of drug development and materials science.
Furthermore, in the field of medicine, N-chloro-N-cyclohexylbenzenesulfonamide also has extraordinary performance. In some drug synthesis routes, it is an important intermediate. It participates in the construction of drug molecules and can endow drugs with specific biological activities and physicochemical properties. For example, by reacting with other compounds, the fat solubility and water solubility of drug molecules can be changed, which in turn affects the absorption, distribution, metabolism and excretion process of drugs, and improves the efficacy and safety of drugs.
In addition, due to its chlorination properties, it may play a role in the development of some antibacterial and disinfectant products. By releasing active chlorine, it destroys the structure and function of bacteria, viruses and other microorganisms, achieving the purpose of antibacterial disinfection, and is used for the development of medical and health and related products, or as a potential raw material.
In organic synthesis, this compound is often used as a chlorination agent to introduce chlorine atoms into organic molecules. Due to its structural characteristics, it can provide an active chlorine source and participate in a variety of chemical reactions. For example, under specific reaction conditions, it can selectively chlorinate hydrogen at the allyl or benzyl sites. This chlorination reaction has high regioselectivity and chemical selectivity, which can accurately achieve the construction of target molecules. When synthesizing complex organic compounds, it is a key step to help chemists obtain the desired structure to meet the needs of specific structural compounds in the fields of drug development and materials science.
Furthermore, in the field of medicine, N-chloro-N-cyclohexylbenzenesulfonamide also has extraordinary performance. In some drug synthesis routes, it is an important intermediate. It participates in the construction of drug molecules and can endow drugs with specific biological activities and physicochemical properties. For example, by reacting with other compounds, the fat solubility and water solubility of drug molecules can be changed, which in turn affects the absorption, distribution, metabolism and excretion process of drugs, and improves the efficacy and safety of drugs.
In addition, due to its chlorination properties, it may play a role in the development of some antibacterial and disinfectant products. By releasing active chlorine, it destroys the structure and function of bacteria, viruses and other microorganisms, achieving the purpose of antibacterial disinfection, and is used for the development of medical and health and related products, or as a potential raw material.
What are the physical properties of N-chloro-n-cyclohexylbenzenesulfonamide?
N-Chloro-N-cyclohexylbenzenesulfonamide is also an organic compound. It has specific physical properties, which are related to the state of the substance, the melting boiling point, the solubility and other characteristics, which are all important for recognizing its properties.
In terms of its physical state, it is usually in a solid state at room temperature, and the quality is relatively stable. Its melting point is about [X] ° C. This temperature is the boundary point at which it changes from solid to liquid state. The determination of the melting point can help the separation of purity. If there are many impurities, the melting point drops and the melting range is wide.
As for the boiling point, it reaches about [X] ° C. Under a specific pressure, the temperature at which the substance changes from liquid to gas state is also the temperature. The boiling point is related to the intermolecular force, and the shape of the intermolecular force of this compound can be seen from the boiling point.
In terms of solubility, it has a certain solubility in organic solvents such as ethanol and ether. Due to the principle of "similarity and miscibility", its molecular structure is similar to that of organic solvents, so it can be miscible. However, in water, the solubility is very small, because its molecular polarity is quite different from water, and it is difficult for water molecules to form an effective effect.
Density is also an important physical property, about [X] g/cm ³. This value reflects its mass per unit volume. Compared with other substances, it can be judged as light and heavy.
In addition, the appearance is often white crystalline powder, which is convenient for preliminary identification. These physical properties, in the fields of organic synthesis, chemical production, etc., have the ability to guide the key, and can help practitioners choose and apply methods to use, control, and preserve them.
In terms of its physical state, it is usually in a solid state at room temperature, and the quality is relatively stable. Its melting point is about [X] ° C. This temperature is the boundary point at which it changes from solid to liquid state. The determination of the melting point can help the separation of purity. If there are many impurities, the melting point drops and the melting range is wide.
As for the boiling point, it reaches about [X] ° C. Under a specific pressure, the temperature at which the substance changes from liquid to gas state is also the temperature. The boiling point is related to the intermolecular force, and the shape of the intermolecular force of this compound can be seen from the boiling point.
In terms of solubility, it has a certain solubility in organic solvents such as ethanol and ether. Due to the principle of "similarity and miscibility", its molecular structure is similar to that of organic solvents, so it can be miscible. However, in water, the solubility is very small, because its molecular polarity is quite different from water, and it is difficult for water molecules to form an effective effect.
Density is also an important physical property, about [X] g/cm ³. This value reflects its mass per unit volume. Compared with other substances, it can be judged as light and heavy.
In addition, the appearance is often white crystalline powder, which is convenient for preliminary identification. These physical properties, in the fields of organic synthesis, chemical production, etc., have the ability to guide the key, and can help practitioners choose and apply methods to use, control, and preserve them.
What is the chemistry of N-chloro-n-cyclohexylbenzenesulfonamide?
The chemical properties of N-chloro-N-cyclohexylbenzenesulfonamide are fascinating. This substance has unique reactivity.
It is often used as a chlorination reagent in the field of organic synthesis. Due to its structure containing chlorine atoms and being connected to nitrogen atoms, chlorine atoms are quite active and can participate in many nucleophilic substitution reactions. If they meet electron-rich aromatic compounds, chlorine atoms may be replaced by aromatic rings, thereby forming new carbon-chlorine bonds. This reaction is an effective way to synthesize specific aromatic chlorides.
And its stability is also considerable. Although it contains active chlorine atoms, it can remain relatively stable at room temperature without specific initiation conditions. However, under extreme conditions such as high temperature, strong alkali or strong reducing agent, the structure may change. In alkaline media, the nitrogen-chlorine bond is easily attacked by hydroxide ions, causing chlorine atoms to leave and form corresponding substitution products.
In terms of solubility, it has good solubility in common organic solvents such as dichloromethane, chloroform, tetrahydrofuran, etc. This property facilitates its uniform dispersion in the organic reaction system and promotes the smooth progress of the reaction.
And the reaction selectivity of this substance is quite good. In the synthesis of some complex organic molecules, chlorine atoms can be introduced precisely at specific positions to achieve the expected molecular structure, providing powerful tools for organic synthesis chemists to prepare complex organic compounds with specific functions.
It is often used as a chlorination reagent in the field of organic synthesis. Due to its structure containing chlorine atoms and being connected to nitrogen atoms, chlorine atoms are quite active and can participate in many nucleophilic substitution reactions. If they meet electron-rich aromatic compounds, chlorine atoms may be replaced by aromatic rings, thereby forming new carbon-chlorine bonds. This reaction is an effective way to synthesize specific aromatic chlorides.
And its stability is also considerable. Although it contains active chlorine atoms, it can remain relatively stable at room temperature without specific initiation conditions. However, under extreme conditions such as high temperature, strong alkali or strong reducing agent, the structure may change. In alkaline media, the nitrogen-chlorine bond is easily attacked by hydroxide ions, causing chlorine atoms to leave and form corresponding substitution products.
In terms of solubility, it has good solubility in common organic solvents such as dichloromethane, chloroform, tetrahydrofuran, etc. This property facilitates its uniform dispersion in the organic reaction system and promotes the smooth progress of the reaction.
And the reaction selectivity of this substance is quite good. In the synthesis of some complex organic molecules, chlorine atoms can be introduced precisely at specific positions to achieve the expected molecular structure, providing powerful tools for organic synthesis chemists to prepare complex organic compounds with specific functions.
What is N-chloro-n-cyclohexylbenzenesulfonamide production method?
The ancient method for the preparation of N-chloro-N-cyclohexylbenzenesulfonamide has its delicacy. First take benzenesulfonyl chloride, place it in a clean kettle, and slowly drop it with cyclohexylamine. When dripping, the temperature should be carefully controlled, so as not to overheat, so as to prevent side reactions. In these two cases, the acylation process is initiated to form N-cyclohexylbenzenesulfonamide.
Then, take the obtained N-cyclohexylbenzenesulfonamide and dissolve it in a suitable solvent, such as dichloromethane or chloroform. Another chlorine-containing reagent, such as sodium hypochlorite solution, is slowly added. In addition, it is still necessary to pay attention to the temperature and Chlorine is combined with the nitrogen atom in N-cyclohexylbenzenesulfonamide to give N-chloro-N-cyclohexylbenzenesulfonamide.
After the reaction is completed, the product is separated and purified by the usual method. Or by extraction, the product is extracted from the reaction solution; or by recrystallization, the product is purified. In this way, N-chloro-N-cyclohexylbenzenesulfonamide can be prepared to meet the needs.
Then, take the obtained N-cyclohexylbenzenesulfonamide and dissolve it in a suitable solvent, such as dichloromethane or chloroform. Another chlorine-containing reagent, such as sodium hypochlorite solution, is slowly added. In addition, it is still necessary to pay attention to the temperature and Chlorine is combined with the nitrogen atom in N-cyclohexylbenzenesulfonamide to give N-chloro-N-cyclohexylbenzenesulfonamide.
After the reaction is completed, the product is separated and purified by the usual method. Or by extraction, the product is extracted from the reaction solution; or by recrystallization, the product is purified. In this way, N-chloro-N-cyclohexylbenzenesulfonamide can be prepared to meet the needs.
What are the precautions when using N-chloro-n-cyclohexylbenzenesulfonamide?
N-Chloro-N-cyclohexylbenzenesulfonamide, when using it, there are various things to pay attention to. This agent has unique properties and its chemical activity is quite high. When using it, it should be used with care. Appropriate protective equipment, such as gloves, goggles, protective clothing, etc., should be worn to prevent it from touching the skin, entering the eyes, covering it or causing skin irritation or burns. If it enters the eyes, it will be more harmful.
Furthermore, the dosage in the reaction system needs to be precisely controlled. Excessive use, or excessive reaction, produces many by-products, affecting the purity and yield of the target product; if the dosage is too small, the reaction will be difficult to achieve expectations, or the reaction will be delayed or even unable to occur completely.
And because it has a certain degree of oxidation, storage and use should avoid coexistence with reducing substances, otherwise it may cause violent reactions and lead to danger. And its stability should also be paid attention to, it should be stored in a cool, dry and well-ventilated place, protected from heat and moisture, to prevent its decomposition and deterioration, and lose its due effect.
The place of use should also be well ventilated, if used in a closed space, the volatile gas will accumulate, or cause poisoning and other hazards. At the same time, appropriate reaction conditions are required during operation, such as temperature, pH, etc., which have a significant impact on the reaction process and effect. Careful treatment is required according to the specific reaction in order to obtain good reaction results and ensure safe and efficient use.
Furthermore, the dosage in the reaction system needs to be precisely controlled. Excessive use, or excessive reaction, produces many by-products, affecting the purity and yield of the target product; if the dosage is too small, the reaction will be difficult to achieve expectations, or the reaction will be delayed or even unable to occur completely.
And because it has a certain degree of oxidation, storage and use should avoid coexistence with reducing substances, otherwise it may cause violent reactions and lead to danger. And its stability should also be paid attention to, it should be stored in a cool, dry and well-ventilated place, protected from heat and moisture, to prevent its decomposition and deterioration, and lose its due effect.
The place of use should also be well ventilated, if used in a closed space, the volatile gas will accumulate, or cause poisoning and other hazards. At the same time, appropriate reaction conditions are required during operation, such as temperature, pH, etc., which have a significant impact on the reaction process and effect. Careful treatment is required according to the specific reaction in order to obtain good reaction results and ensure safe and efficient use.
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