Linshang Chemical
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4-Amino-6-(Trichloroethenyl)-1,3-Benzenedisulfonamide
Linshang Chemical
|
HS Code |
568155 |
| Chemical Formula | C8H6Cl3N3O4S2 |
| Molar Mass | 388.64 g/mol |
As an accredited 4-Amino-6-(Trichloroethenyl)-1,3-Benzenedisulfonamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 4 - amino - 6 - (trichloroethenyl)-1,3 - benzenedisulfonamide in sealed chemical - grade bags. |
| Storage | Store 4 - amino - 6 - (trichloroethenyl)-1,3 - benzenedisulfonamide in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and incompatible substances such as strong oxidizing agents. Use a tightly sealed container to prevent moisture absorption and potential degradation, ensuring its stability during storage. |
| Shipping | Ship 4 - amino - 6 - (trichloroethenyl)-1,3 - benzenedisulfonamide in properly sealed, corrosion - resistant containers. Ensure compliance with chemical shipping regulations, and label clearly for safe and proper transportation. |
Competitive 4-Amino-6-(Trichloroethenyl)-1,3-Benzenedisulfonamide 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-Amino-6-(Trichloroethenyl)-1,3-Benzenedisulfonamide in China?
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What is the chemical structure of 4 - amino - 6 - (trichloroethenyl) -1,3 - benzenedisulfonamide?
This is the question of 4-amino-6- (trichlorovinyl) -1,3-benzene disulfonamide. To know its chemical structure. The structure of this compound is based on a benzene ring, with a disulfonamide group at the upper 1,3 positions, an amino group at the 4th position, and a trichlorovinyl group at the 6th position. For the benzene ring, the six-membered carbon ring has a conjugated double bond and has a stable planar structure. Sulfonamide group, which is linked to a sulfonyl group and an amino group, has a specific chemical activity. The amino group is a nitrogen atom connected to a dihydrogen atom, which is basic and can participate in the reaction. Trichlorovinyl, a vinyl group containing trichlorine substitution, has the characteristics of unsaturation and chlorine Its overall structure determines the physical and chemical properties of the compound, and it may have specific uses and reactivity in the fields of organic synthesis, drug development, etc. In this way, the chemical structure of 4-amino-6- (trichlorovinyl) -1,3-benzenedisulfonamide is roughly.
What are the physical properties of 4 - amino - 6 - (trichloroethenyl) -1,3 - benzenedisulfonamide?
4-Amino-6- (trichlorovinyl) -1,3-benzenediesulfonamide, an organic compound. Its physical properties are as follows:
Under normal conditions, it is a white to light yellow crystalline powder. This color state is derived from the absorption and reflection characteristics of the molecular structure. The powder is formed by intermolecular forces and crystallization habits.
Smell, or has a weak special odor. This odor is volatilized by specific chemical groups in the molecule and is sensed by nasal olfactory receptors.
Touch it, the texture is fine, because the particles are small and uniform, and the friction between the powder particles is small.
As for the melting point, it has been experimentally determined to be about [X] ° C. The melting point is restricted by intermolecular forces, such as hydrogen bonds, van der Waals forces, etc. At this temperature, the molecule is able to break through the lattice binding and transform from solid to liquid.
In terms of solubility, the solubility in water is limited. Although the molecule contains polar sulfonamide groups, trichlorovinyl is non-polar, the overall polarity is not strong, and the interaction with water is weak. However, in some organic solvents such as dimethyl sulfoxide (DMSO), N, N-dimethyl formamide (DMF), the solubility is relatively high, because the polarity of the two is matched with the compound, which can form a strong interaction with the molecule and help it disperse and dissolve.
In addition, its density is about [X] g/cm ³, and the density reflects the mass of the substance per unit volume, which is determined by the molecular mass and the packing compactness. The molecular mass of the compound interacts with the spatial arrangement to present this density value.
Under normal conditions, it is a white to light yellow crystalline powder. This color state is derived from the absorption and reflection characteristics of the molecular structure. The powder is formed by intermolecular forces and crystallization habits.
Smell, or has a weak special odor. This odor is volatilized by specific chemical groups in the molecule and is sensed by nasal olfactory receptors.
Touch it, the texture is fine, because the particles are small and uniform, and the friction between the powder particles is small.
As for the melting point, it has been experimentally determined to be about [X] ° C. The melting point is restricted by intermolecular forces, such as hydrogen bonds, van der Waals forces, etc. At this temperature, the molecule is able to break through the lattice binding and transform from solid to liquid.
In terms of solubility, the solubility in water is limited. Although the molecule contains polar sulfonamide groups, trichlorovinyl is non-polar, the overall polarity is not strong, and the interaction with water is weak. However, in some organic solvents such as dimethyl sulfoxide (DMSO), N, N-dimethyl formamide (DMF), the solubility is relatively high, because the polarity of the two is matched with the compound, which can form a strong interaction with the molecule and help it disperse and dissolve.
In addition, its density is about [X] g/cm ³, and the density reflects the mass of the substance per unit volume, which is determined by the molecular mass and the packing compactness. The molecular mass of the compound interacts with the spatial arrangement to present this density value.
What are the main uses of 4 - amino - 6 - (trichloroethenyl) -1,3 - benzenedisulfonamide?
4+-+amino+-+6+-+%28trichloroethenyl%29-1%2C3+-+benzenedisulfonamide is 4-amino-6- (trichlorovinyl) -1,3-benzene disulfonamide, which is widely used.
In the field of medicine, it can be used as a key intermediate for drug research and development. The Gain structure contains special functional groups that can interact with specific biomolecules in the body. Or by binding to protein targets, it affects its biological activity, thus exploring new ways for disease treatment. For example, in the development of some targeted drugs, it can be used as a starting material. After a series of chemical modifications, compounds with specific pharmacological activities are obtained, which are expected to be used in the treatment of cancer, inflammation and other diseases.
In the field of agriculture, or can be made into special pesticide ingredients. By interfering with the specific physiological processes of insects and pathogens, it exhibits insecticidal and bactericidal effects. Due to its unique structure, it may be able to develop high-efficiency, low-toxicity and environmentally friendly pesticides to help control crop diseases and insect pests and improve agricultural yield and quality.
In the field of materials science, it also has potential applications. Or it can be used to prepare special functional polymer materials. Because it contains active groups such as sulfonamide groups, it can react with polymers, giving materials such as antistatic, hydrophilic and other special properties. It can be used to manufacture high-performance fibers, coatings, etc., to expand the application scenarios of materials.
also participates in the construction of new compounds because it contains trichlorovinyl, or is used as a special reaction reagent in chemical synthesis, opening up new paths for organic synthetic chemistry and promoting innovation and development in related fields.
In the field of medicine, it can be used as a key intermediate for drug research and development. The Gain structure contains special functional groups that can interact with specific biomolecules in the body. Or by binding to protein targets, it affects its biological activity, thus exploring new ways for disease treatment. For example, in the development of some targeted drugs, it can be used as a starting material. After a series of chemical modifications, compounds with specific pharmacological activities are obtained, which are expected to be used in the treatment of cancer, inflammation and other diseases.
In the field of agriculture, or can be made into special pesticide ingredients. By interfering with the specific physiological processes of insects and pathogens, it exhibits insecticidal and bactericidal effects. Due to its unique structure, it may be able to develop high-efficiency, low-toxicity and environmentally friendly pesticides to help control crop diseases and insect pests and improve agricultural yield and quality.
In the field of materials science, it also has potential applications. Or it can be used to prepare special functional polymer materials. Because it contains active groups such as sulfonamide groups, it can react with polymers, giving materials such as antistatic, hydrophilic and other special properties. It can be used to manufacture high-performance fibers, coatings, etc., to expand the application scenarios of materials.
also participates in the construction of new compounds because it contains trichlorovinyl, or is used as a special reaction reagent in chemical synthesis, opening up new paths for organic synthetic chemistry and promoting innovation and development in related fields.
What are the synthesis methods of 4 - amino - 6 - (trichloroethenyl) -1,3 - benzenedisulfonamide?
To prepare 4 + - + amino- + 6 + - + （ trichlorovinyl) - 1,3 + -benzene disulfonamide, there are various methods.
First, benzene can be taken as the starting material, and benzene can be co-heated with concentrated sulfuric acid by sulfonation method. After ingenious temperature control and reaction time, benzene sulfonic acid can be obtained. Then, in a specific reaction environment, a reagent containing trichlorovinyl is introduced, and with the help of a suitable catalyst, the trichlorovinyl is connected to the specific position of benzene sulfonic acid to form a benzene sulfonic acid derivative containing trichlorovinyl. Then in the method of amination, the amino group is introduced with suitable amination reagents, such as ammonia gas, amine compounds, etc., and the amino group is introduced under appropriate reaction conditions to obtain the target product.
Second, benzene derivatives containing specific substituents can also be selected as starting materials. If the starting material already has some of the desired substituents, and only amino groups and trichlorovinyl groups are not introduced, trichlorovinyl and amino groups can be introduced in sequence. When introducing trichlorovinyl, depending on the structure of the raw materials, nucleophilic substitution, electrophilic substitution and other methods are selected to reasonably select the reaction reagents and conditions. After trichlorovinyl is connected, amino groups are introduced by amination. In this process, it is crucial to control the reaction conditions, such as temperature, pH, reaction time, etc., which need to be carefully regulated to prevent side reactions from breeding and ensure the purity and yield of the product.
Third, the method of gradually constructing the benzene ring can be used. First, the benzene ring precursor containing the desired substituent is constructed by organic synthesis. For example, a multi-step reaction is used to gradually connect simple organic compounds to form an unsaturated ring structure with a specific substitution mode. After appropriate reaction, it is converted into a benzene ring, and amino groups and trichlorovinyl groups are introduced simultaneously or step by step. Although this path is complicated, it has advantages for precise control of the product structure. If the reaction route can be properly planned, 4 + - + amino - + 6 + - + （ trichlorovinyl) -1,3 + -benzenesulfonamide can be efficiently prepared.
First, benzene can be taken as the starting material, and benzene can be co-heated with concentrated sulfuric acid by sulfonation method. After ingenious temperature control and reaction time, benzene sulfonic acid can be obtained. Then, in a specific reaction environment, a reagent containing trichlorovinyl is introduced, and with the help of a suitable catalyst, the trichlorovinyl is connected to the specific position of benzene sulfonic acid to form a benzene sulfonic acid derivative containing trichlorovinyl. Then in the method of amination, the amino group is introduced with suitable amination reagents, such as ammonia gas, amine compounds, etc., and the amino group is introduced under appropriate reaction conditions to obtain the target product.
Second, benzene derivatives containing specific substituents can also be selected as starting materials. If the starting material already has some of the desired substituents, and only amino groups and trichlorovinyl groups are not introduced, trichlorovinyl and amino groups can be introduced in sequence. When introducing trichlorovinyl, depending on the structure of the raw materials, nucleophilic substitution, electrophilic substitution and other methods are selected to reasonably select the reaction reagents and conditions. After trichlorovinyl is connected, amino groups are introduced by amination. In this process, it is crucial to control the reaction conditions, such as temperature, pH, reaction time, etc., which need to be carefully regulated to prevent side reactions from breeding and ensure the purity and yield of the product.
Third, the method of gradually constructing the benzene ring can be used. First, the benzene ring precursor containing the desired substituent is constructed by organic synthesis. For example, a multi-step reaction is used to gradually connect simple organic compounds to form an unsaturated ring structure with a specific substitution mode. After appropriate reaction, it is converted into a benzene ring, and amino groups and trichlorovinyl groups are introduced simultaneously or step by step. Although this path is complicated, it has advantages for precise control of the product structure. If the reaction route can be properly planned, 4 + - + amino - + 6 + - + （ trichlorovinyl) -1,3 + -benzenesulfonamide can be efficiently prepared.
4 - amino - 6 - (trichloroethenyl) -1,3 - benzenedisulfonamide What are the precautions during use?
4-Amino-6- (trichlorovinyl) -1,3-benzenediesulfonamide is a rather special chemical substance, and there are indeed many things to pay attention to during use.
Bear the brunt, and safety protection must not be forgotten. This substance may be toxic and irritating, and it may cause discomfort or even damage when it touches the skin, eyes or inhales its dust and vapor. Therefore, when using it, be sure to wear suitable protective equipment, such as protective gloves, protective glasses and gas masks, to avoid direct contact and inhalation.
Furthermore, the operating environment is also extremely critical. The relevant operation should be carried out in a well-ventilated place. It is best to have local ventilation facilities to facilitate the timely discharge of harmful gases that may be generated, reduce the concentration of harmful substances in the air, and reduce the harm to the human body.
In addition, caution is also required in storage. It should be stored in a cool, dry and ventilated place, away from fire, heat and incompatible substances. It is necessary to strictly follow the chemical storage specifications to prevent accidental reactions, such as mixing with certain strong oxidants, acids, alkalis and other substances, or causing severe reactions.
During use, precise control of the dosage is also the key. It should be calculated and used accurately according to actual needs to avoid waste, and at the same time prevent subsequent treatment problems due to excessive dosage, or cause excessive pressure on the environment.
And in the event of a leak, do not panic. Emergency treatment procedures should be initiated immediately, and irrelevant personnel should be quickly evacuated to isolate the leakage area. According to the scale of the leak and the actual situation, choose appropriate methods for cleaning, such as using inert adsorption materials for adsorption, and then properly collect and dispose of the adsorption.
When using 4-amino-6- (trichlorovinyl) -1,3-benzenesulfonamide, all aspects need to be treated with caution. A little negligence may cause safety and environmental problems.
Bear the brunt, and safety protection must not be forgotten. This substance may be toxic and irritating, and it may cause discomfort or even damage when it touches the skin, eyes or inhales its dust and vapor. Therefore, when using it, be sure to wear suitable protective equipment, such as protective gloves, protective glasses and gas masks, to avoid direct contact and inhalation.
Furthermore, the operating environment is also extremely critical. The relevant operation should be carried out in a well-ventilated place. It is best to have local ventilation facilities to facilitate the timely discharge of harmful gases that may be generated, reduce the concentration of harmful substances in the air, and reduce the harm to the human body.
In addition, caution is also required in storage. It should be stored in a cool, dry and ventilated place, away from fire, heat and incompatible substances. It is necessary to strictly follow the chemical storage specifications to prevent accidental reactions, such as mixing with certain strong oxidants, acids, alkalis and other substances, or causing severe reactions.
During use, precise control of the dosage is also the key. It should be calculated and used accurately according to actual needs to avoid waste, and at the same time prevent subsequent treatment problems due to excessive dosage, or cause excessive pressure on the environment.
And in the event of a leak, do not panic. Emergency treatment procedures should be initiated immediately, and irrelevant personnel should be quickly evacuated to isolate the leakage area. According to the scale of the leak and the actual situation, choose appropriate methods for cleaning, such as using inert adsorption materials for adsorption, and then properly collect and dispose of the adsorption.
When using 4-amino-6- (trichlorovinyl) -1,3-benzenesulfonamide, all aspects need to be treated with caution. A little negligence may cause safety and environmental problems.
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