Linshang Chemical
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4-[[(4-Chlorobutyl)Sulphonyl]Amino]Benzenesulphonamide
Linshang Chemical
|
HS Code |
510155 |
| Chemical Formula | C10H15ClN2O4S2 |
| Molecular Weight | 326.82 |
As an accredited 4-[[(4-Chlorobutyl)Sulphonyl]Amino]Benzenesulphonamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 4 -[(4 -chlorobutyl)sulphonyl]amino]benzenesulphonamide in sealed chemical - grade bags. |
| Storage | 4 - [(4 - chlorobutyl)sulphonyl]amino benzenesulphonamide should be stored in a cool, dry place, away from heat sources and direct sunlight. Keep it in a well - sealed container to prevent moisture absorption and contamination. Store separately from incompatible substances, such as strong oxidizing agents, to avoid potential chemical reactions. |
| Shipping | 4 - [(4 - chlorobutyl)sulphonyl]amino benzenesulphonamide is shipped in well - sealed, corrosion - resistant containers. Shipment adheres to strict chemical transportation regulations, ensuring safety during transit to prevent any spills or hazards. |
Competitive 4-[[(4-Chlorobutyl)Sulphonyl]Amino]Benzenesulphonamide prices that fit your budget—flexible terms and customized quotes for every order.
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Where to Buy 4-[[(4-Chlorobutyl)Sulphonyl]Amino]Benzenesulphonamide in China?
As a trusted 4-[[(4-Chlorobutyl)Sulphonyl]Amino]Benzenesulphonamide manufacturer, we deliver:
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What is the chemical structure of 4- [ (4-chlorobutyl) sulphonyl] amino] benzenesulphonamide?
This is an investigation into the chemical structure of 4- [ (4-chlorobutyl) sulfonyl] aminobenzenesulfonamide. This compound is based on a benzene ring with a disulfonamide group attached to it. The nitrogen atom of the monosulfonamide group is connected to the (4-chlorobutyl) sulfonyl group, and the (4-chlorobutyl) chlorine atom is connected to the butyl terminal. The other sulfonamide group is directly connected to the benzene ring.
Specifically, the benzene ring is a hexamembered carbon ring with a conjugated double bond, giving it special stability. A sulfonamide group is composed of a sulfonyl group (-SO 2O -) connected to an amino group (-NH -), which is connected to a specific position in the benzene ring. The (4-chlorobutyl) sulfonyl group, the butyl group is a linear alkyl group containing four carbons, which is connected to a chlorine atom at one end and a sulfonyl group at the other end, and then to the nitrogen atom of the sulfonamide group on the benzene ring.
This chemical structure has attracted much attention in the fields of organic synthesis and medicinal chemistry. The properties and interactions of different groups in its structure affect the physical, chemical properties and biological activities of compounds. For example, the electronegativity of the chlorine atom affects the molecular polarity and reactivity; the sulfonamide group can participate in the formation of hydrogen bonds, which affects the solubility and biological activity Exploring this structure is of great significance for understanding its properties and developing related applications.
Specifically, the benzene ring is a hexamembered carbon ring with a conjugated double bond, giving it special stability. A sulfonamide group is composed of a sulfonyl group (-SO 2O -) connected to an amino group (-NH -), which is connected to a specific position in the benzene ring. The (4-chlorobutyl) sulfonyl group, the butyl group is a linear alkyl group containing four carbons, which is connected to a chlorine atom at one end and a sulfonyl group at the other end, and then to the nitrogen atom of the sulfonamide group on the benzene ring.
This chemical structure has attracted much attention in the fields of organic synthesis and medicinal chemistry. The properties and interactions of different groups in its structure affect the physical, chemical properties and biological activities of compounds. For example, the electronegativity of the chlorine atom affects the molecular polarity and reactivity; the sulfonamide group can participate in the formation of hydrogen bonds, which affects the solubility and biological activity Exploring this structure is of great significance for understanding its properties and developing related applications.
What are the main uses of 4- [ (4-chlorobutyl) sulphonyl] amino] benzenesulphonamide?
4 - [ [ （ 4-chlorobutyl) sulfonyl] amino] benzenesulfonamide is an organic compound. Its main uses are quite extensive, and it has important applications in many fields.
In the field of medicine, this compound may have potential pharmacological activity. Chemists and pharmacologists often explore its therapeutic effect on specific diseases. Or by modifying and modifying its chemical structure, new drugs can be developed to treat diseases such as inflammation and tumors. Because of its special molecular structure, it may interact with specific biomacromolecules in the body, such as proteins and enzymes, so as to regulate the physiological and biochemical processes in organisms and achieve the purpose of treating diseases.
In the field of materials science, 4 - [ [ （ 4-chloroprene) sulfonyl] amino] benzenesulfonamide may also have unique uses. It can also be used as a functional additive and added to polymer materials to improve the properties of materials. For example, to enhance the stability and durability of materials, or to change the surface properties of materials to make them more hydrophilic or hydrophobic, thereby broadening the application range of materials and playing a role in industrial production such as plastics and rubber.
In addition, in the field of organic synthesis chemistry, this compound can be used as a key intermediate. With its active functional groups, it can be linked and transformed with other organic compounds through a series of chemical reactions to construct more complex organic molecular structures. Organic synthesis chemists can use 4 - [ [ （ 4-chlorobutyl) sulfonyl] amino] benzenesulfonamide to synthesize various organic compounds with special functions and structures through carefully designed synthesis routes, providing an important material basis for the development of organic synthesis chemistry.
In the field of medicine, this compound may have potential pharmacological activity. Chemists and pharmacologists often explore its therapeutic effect on specific diseases. Or by modifying and modifying its chemical structure, new drugs can be developed to treat diseases such as inflammation and tumors. Because of its special molecular structure, it may interact with specific biomacromolecules in the body, such as proteins and enzymes, so as to regulate the physiological and biochemical processes in organisms and achieve the purpose of treating diseases.
In the field of materials science, 4 - [ [ （ 4-chloroprene) sulfonyl] amino] benzenesulfonamide may also have unique uses. It can also be used as a functional additive and added to polymer materials to improve the properties of materials. For example, to enhance the stability and durability of materials, or to change the surface properties of materials to make them more hydrophilic or hydrophobic, thereby broadening the application range of materials and playing a role in industrial production such as plastics and rubber.
In addition, in the field of organic synthesis chemistry, this compound can be used as a key intermediate. With its active functional groups, it can be linked and transformed with other organic compounds through a series of chemical reactions to construct more complex organic molecular structures. Organic synthesis chemists can use 4 - [ [ （ 4-chlorobutyl) sulfonyl] amino] benzenesulfonamide to synthesize various organic compounds with special functions and structures through carefully designed synthesis routes, providing an important material basis for the development of organic synthesis chemistry.
What are the physical properties of 4- [ (4-chlorobutyl) sulphonyl] amino] benzenesulphonamide?
4 - [ [( 4 -Chlorobutyl) sulfonyl] amino] benzenesulfonamide, this is an organic compound. Its physical properties are very critical, and it is related to many uses and characteristics of this compound.
First of all, its appearance is often white to white solid powder under normal temperature and pressure. This form is easy to store and transport, and it is easy to disperse and participate in reactions in many reaction systems. Its white color reflects that the compound has high purity and few impurities. It is crucial in some fields that require strict purity, such as pharmaceutical synthesis.
Besides, its melting point is about a specific temperature range. Melting point is an important physical index of the compound, which can be used to identify its purity. If the compound has high purity, the melting point range is usually narrow; conversely, if it contains impurities, the melting point will not only decrease, but also the range will be widened. By accurately measuring the melting point, the quality of the compound can be preliminarily judged.
Its solubility is also an important physical property. In organic solvents, such as common ethanol, acetone, etc., it has a certain solubility. This property makes it possible to participate in various reactions in the corresponding solvent system as a reactant or product in organic synthesis. In water, its solubility is relatively low, and this difference determines that in the process of separation and purification, water and organic solvents can be used for extraction to separate the compound from other impurities.
In addition, the density of the compound also has a specific value. Density, as one of the physical properties, may not receive much attention in general chemical reactions, but it is crucial when it comes to practical application scenarios such as material ratio and storage container selection. Knowing its density can accurately calculate the quality of a certain volume of the compound and provide a basis for actual production operations.
In summary, the physical properties of 4 - [ [( 4-chlorobutyl) sulfonyl] amino] benzenesulfonamide, from appearance, melting point, solubility to density, have a profound impact on its application in scientific research, industrial production and many other fields, and are of great significance for in-depth understanding and rational use of this compound.
First of all, its appearance is often white to white solid powder under normal temperature and pressure. This form is easy to store and transport, and it is easy to disperse and participate in reactions in many reaction systems. Its white color reflects that the compound has high purity and few impurities. It is crucial in some fields that require strict purity, such as pharmaceutical synthesis.
Besides, its melting point is about a specific temperature range. Melting point is an important physical index of the compound, which can be used to identify its purity. If the compound has high purity, the melting point range is usually narrow; conversely, if it contains impurities, the melting point will not only decrease, but also the range will be widened. By accurately measuring the melting point, the quality of the compound can be preliminarily judged.
Its solubility is also an important physical property. In organic solvents, such as common ethanol, acetone, etc., it has a certain solubility. This property makes it possible to participate in various reactions in the corresponding solvent system as a reactant or product in organic synthesis. In water, its solubility is relatively low, and this difference determines that in the process of separation and purification, water and organic solvents can be used for extraction to separate the compound from other impurities.
In addition, the density of the compound also has a specific value. Density, as one of the physical properties, may not receive much attention in general chemical reactions, but it is crucial when it comes to practical application scenarios such as material ratio and storage container selection. Knowing its density can accurately calculate the quality of a certain volume of the compound and provide a basis for actual production operations.
In summary, the physical properties of 4 - [ [( 4-chlorobutyl) sulfonyl] amino] benzenesulfonamide, from appearance, melting point, solubility to density, have a profound impact on its application in scientific research, industrial production and many other fields, and are of great significance for in-depth understanding and rational use of this compound.
What is the synthesis method of 4- [[ (4-chlorobutyl) sulphonyl] amino] benzenesulphonamide?
To prepare 4 - [ [( 4-chlorobutyl) sulfonyl] amino] benzenesulfonamide, the method is as follows:
Take benzenesulfonamide as the starting material and react with the appropriate sulfonylation reagent. This sulfonylation reagent can be selected as 4-chlorobutyl sulfonyl chloride. In a suitable reaction environment, the two meet, and the amino group of benzenesulfonamide and the acid chloride group of 4-chlorobutyl sulfonyl chloride combine to form a new bond according to the mechanism of nucleophilic substitution.
When reacting, pay attention to the choice of solvent. Commonly selected such as dichloromethane, N, N-dimethylformamide, etc., because it dissolves the reactants well and has no obvious hindrance to the reaction. The reaction temperature is also critical, or at a low temperature, such as 0 ° C to 5 ° C, and then gradually rise to room temperature, so that the reaction can proceed slowly and orderly. In the reaction system, or add an acid binding agent, such as triethylamine, to remove the acid generated by the reaction and promote the right balance of the reaction.
After the reaction is completed, the product is purified by conventional separation and purification methods, such as column chromatography, recrystallization method, etc. The column chromatography method can be separated according to the difference in the partition coefficient between the product and the impurities in the stationary phase and the mobile phase; the recrystallization method selects a suitable solvent to dissolve the product in the hot solution, and the crystallization precipitates after cooling. The impurities remain in the mother liquor, so the pure 4 - [ [( 4-chlorobutyl) sulfonyl] amino] benzenesulfonamide can be obtained. In this way, this compound can be prepared.
Take benzenesulfonamide as the starting material and react with the appropriate sulfonylation reagent. This sulfonylation reagent can be selected as 4-chlorobutyl sulfonyl chloride. In a suitable reaction environment, the two meet, and the amino group of benzenesulfonamide and the acid chloride group of 4-chlorobutyl sulfonyl chloride combine to form a new bond according to the mechanism of nucleophilic substitution.
When reacting, pay attention to the choice of solvent. Commonly selected such as dichloromethane, N, N-dimethylformamide, etc., because it dissolves the reactants well and has no obvious hindrance to the reaction. The reaction temperature is also critical, or at a low temperature, such as 0 ° C to 5 ° C, and then gradually rise to room temperature, so that the reaction can proceed slowly and orderly. In the reaction system, or add an acid binding agent, such as triethylamine, to remove the acid generated by the reaction and promote the right balance of the reaction.
After the reaction is completed, the product is purified by conventional separation and purification methods, such as column chromatography, recrystallization method, etc. The column chromatography method can be separated according to the difference in the partition coefficient between the product and the impurities in the stationary phase and the mobile phase; the recrystallization method selects a suitable solvent to dissolve the product in the hot solution, and the crystallization precipitates after cooling. The impurities remain in the mother liquor, so the pure 4 - [ [( 4-chlorobutyl) sulfonyl] amino] benzenesulfonamide can be obtained. In this way, this compound can be prepared.
What are the safety precautions for 4- [ (4-chlorobutyl) sulphonyl] amino] benzenesulphonamide?
4 - [[ (4 - chlorobutyl) sulphonyl] amino] benzenesulphonamide is a chemical substance and should be treated with caution due to its safety precautions.
This substance may be chemically active. When in contact, it is necessary to take good protection. If it comes into contact with the skin, it may cause discomfort or even allergies, so be sure to wear appropriate protective clothing and gloves when operating. In case of contact with the skin, rinse with plenty of water immediately and seek medical attention as appropriate.
If it is not carefully entered into the eyes, it is particularly harmful or causes eye damage. Once so, rinse the eyes with plenty of water immediately and seek medical treatment quickly.
Inhalation of dust or vapor from this substance is also risky, or affects the respiratory tract, causing coughing, asthma and other diseases. At the place of operation, be sure to ensure good ventilation, and wear appropriate respiratory protective equipment if necessary.
Furthermore, when storing, it should be placed in a dry, cool and ventilated place, away from fire and heat sources to prevent accidents. At the same time, it should be stored separately from oxidants and acids to avoid mutual reaction.
During use, strictly follow the operating procedures and must not be changed at will. After the experiment, properly dispose of the remaining substances and waste, follow relevant environmental regulations, and do not discard them at will to avoid polluting the environment. In this way, the personal safety and environmental safety of this substance can be ensured when using it.
This substance may be chemically active. When in contact, it is necessary to take good protection. If it comes into contact with the skin, it may cause discomfort or even allergies, so be sure to wear appropriate protective clothing and gloves when operating. In case of contact with the skin, rinse with plenty of water immediately and seek medical attention as appropriate.
If it is not carefully entered into the eyes, it is particularly harmful or causes eye damage. Once so, rinse the eyes with plenty of water immediately and seek medical treatment quickly.
Inhalation of dust or vapor from this substance is also risky, or affects the respiratory tract, causing coughing, asthma and other diseases. At the place of operation, be sure to ensure good ventilation, and wear appropriate respiratory protective equipment if necessary.
Furthermore, when storing, it should be placed in a dry, cool and ventilated place, away from fire and heat sources to prevent accidents. At the same time, it should be stored separately from oxidants and acids to avoid mutual reaction.
During use, strictly follow the operating procedures and must not be changed at will. After the experiment, properly dispose of the remaining substances and waste, follow relevant environmental regulations, and do not discard them at will to avoid polluting the environment. In this way, the personal safety and environmental safety of this substance can be ensured when using it.
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