Linshang Chemical
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N,N-Dichloro-4-Methylbenzenesulfonamide
Linshang Chemical
|
HS Code |
181377 |
| Chemical Formula | C7H7Cl2NO2S |
| Molar Mass | 240.107 g/mol |
| Appearance | Solid (likely white or off - white) |
| Physical State At Room Temp | Solid |
| Odor | May have a characteristic chemical odor |
| Solubility In Water | Low solubility in water |
| Solubility In Organic Solvents | Soluble in some organic solvents like dichloromethane |
| Melting Point | Specific value would require literature search |
| Boiling Point | Specific value would require literature search |
| Stability | Stable under normal conditions, but may react with strong bases or reducing agents |
| Flash Point | Specific value would require literature search |
| Vapor Pressure | Low vapor pressure |
As an accredited N,N-Dichloro-4-Methylbenzenesulfonamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of N,n - dichloro - 4 - methylbenzenesulfonamide in a sealed plastic bag. |
| Storage | **Storage of N,n - dichloro - 4 - methylbenzenesulfonamide** Store N,n - dichloro - 4 - methylbenzenesulfonamide in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and oxidizing agents. Place it in a tightly sealed container to prevent moisture absorption and potential reaction with air components. This helps maintain its chemical integrity and safety during storage. |
| Shipping | N,n - dichloro - 4 - methylbenzenesulfonamide, a chemical, should be shipped in well - sealed, corrosion - resistant containers. Ensure compliance with hazardous material regulations during transportation to prevent spills and ensure safety. |
Competitive N,N-Dichloro-4-Methylbenzenesulfonamide 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
Email: info@alchemist-chem.com
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What is the chemical structure of N, N-dichloro-4-methylbenzenesulfonamide?
N% 2CN + -dioxy-4-methylbenzothiazolinone, this is an organic compound. Its chemical structure is quite complex, let me explain in detail.
The core of this compound is the skeleton of benzothiazolinone. Benzothiazolinone is formed by fusing a benzene ring with a thiazolinone ring. The thiazolinone ring contains heteroatoms such as nitrogen and sulfur, which endow the compound with unique chemical properties.
On the benzothiazolinone skeleton, there is a specific substituent attached. Among them, "4-methyl" indicates the presence of a methyl (-CH 🥰) group at the position of the benzothiazolinone skeleton numbered 4. The introduction of this methyl group affects the physical and chemical properties of the compound, such as solubility and reactivity.
Furthermore, the expression "dioxygen" may imply the existence of two oxygen atoms in the molecular structure. This oxygen atom may be in a ketone carbonyl group, or may exist in other forms, such as hydroxyl groups, ether bonds, etc., which can only be determined by more detailed chemical analysis.
The chemical structure of this compound determines its potential application in the fields of organic synthesis, materials science, and medicinal chemistry. In organic synthesis, it can be used as a key intermediate to build more complex organic molecules; in materials science, or because of its special structure and properties, it exhibits unique optical, electrical and other properties; in the field of medicinal chemistry, or by virtue of its structural characteristics, it interacts with specific targets in organisms to exert pharmacological activity.
The core of this compound is the skeleton of benzothiazolinone. Benzothiazolinone is formed by fusing a benzene ring with a thiazolinone ring. The thiazolinone ring contains heteroatoms such as nitrogen and sulfur, which endow the compound with unique chemical properties.
On the benzothiazolinone skeleton, there is a specific substituent attached. Among them, "4-methyl" indicates the presence of a methyl (-CH 🥰) group at the position of the benzothiazolinone skeleton numbered 4. The introduction of this methyl group affects the physical and chemical properties of the compound, such as solubility and reactivity.
Furthermore, the expression "dioxygen" may imply the existence of two oxygen atoms in the molecular structure. This oxygen atom may be in a ketone carbonyl group, or may exist in other forms, such as hydroxyl groups, ether bonds, etc., which can only be determined by more detailed chemical analysis.
The chemical structure of this compound determines its potential application in the fields of organic synthesis, materials science, and medicinal chemistry. In organic synthesis, it can be used as a key intermediate to build more complex organic molecules; in materials science, or because of its special structure and properties, it exhibits unique optical, electrical and other properties; in the field of medicinal chemistry, or by virtue of its structural characteristics, it interacts with specific targets in organisms to exert pharmacological activity.
What are the main uses of N, N-dichloro-4-methylbenzenesulfonamide
N% 2CN-dioxy-4-methylindoquinone, also known as vitamin K3, did not have this precise chemical name in ancient times, but its related medicinal properties have long been recognized and applied. The main uses of this drug are quite extensive, and the following is a detailed description of Jun.
First, the use of hemostasis. The human body's coagulation mechanism is complex and delicate, and N% 2CN-dioxy-4-methylindoquinone plays a key role in it. It can participate in the synthesis of prothrombin and other coagulation factors in the liver. If the human body lacks this substance, the coagulation process will be blocked, and minor damage may also lead to bleeding. Therefore, in many bleeding diseases, such as neonatal hemorrhage, intestinal malabsorption caused by bleeding, etc., it is often used as medicine to help the coagulation process proceed smoothly and stop bleeding.
Second, the treatment of intestinal diseases. The intestine is the key to human digestion and absorption, and some intestinal diseases will disrupt its normal function. N% 2CN-dioxy-4-methylindoquinone has the function of regulating the flora ecology in the intestine, and can enhance the barrier function of intestinal mucosa. For intestinal diseases such as dysentery and diarrhea, it can relieve symptoms and help the intestine restore health.
Third, it also has important uses in animal husbandry. When livestock and poultry are raised, animals often face health threats due to various factors. Appropriate addition of this substance to feed can prevent bleeding diseases caused by vitamin K deficiency in livestock and poultry, ensure the healthy growth of livestock and poultry, and improve breeding efficiency.
Fourth, it is also used in some specific industrial fields. For example, in some fine chemical synthesis processes, it can be used as an important intermediate to participate in more complex compound synthesis reactions and promote the development of the chemical industry.
N% 2CN-dioxy-4-methylindole quinone Although it has various uses, it should be used with caution. The dosage should be reasonably controlled according to specific conditions and actual needs in order to maximize its effectiveness and avoid adverse reactions.
First, the use of hemostasis. The human body's coagulation mechanism is complex and delicate, and N% 2CN-dioxy-4-methylindoquinone plays a key role in it. It can participate in the synthesis of prothrombin and other coagulation factors in the liver. If the human body lacks this substance, the coagulation process will be blocked, and minor damage may also lead to bleeding. Therefore, in many bleeding diseases, such as neonatal hemorrhage, intestinal malabsorption caused by bleeding, etc., it is often used as medicine to help the coagulation process proceed smoothly and stop bleeding.
Second, the treatment of intestinal diseases. The intestine is the key to human digestion and absorption, and some intestinal diseases will disrupt its normal function. N% 2CN-dioxy-4-methylindoquinone has the function of regulating the flora ecology in the intestine, and can enhance the barrier function of intestinal mucosa. For intestinal diseases such as dysentery and diarrhea, it can relieve symptoms and help the intestine restore health.
Third, it also has important uses in animal husbandry. When livestock and poultry are raised, animals often face health threats due to various factors. Appropriate addition of this substance to feed can prevent bleeding diseases caused by vitamin K deficiency in livestock and poultry, ensure the healthy growth of livestock and poultry, and improve breeding efficiency.
Fourth, it is also used in some specific industrial fields. For example, in some fine chemical synthesis processes, it can be used as an important intermediate to participate in more complex compound synthesis reactions and promote the development of the chemical industry.
N% 2CN-dioxy-4-methylindole quinone Although it has various uses, it should be used with caution. The dosage should be reasonably controlled according to specific conditions and actual needs in order to maximize its effectiveness and avoid adverse reactions.
What are the physical properties of N, N-dichloro-4-methylbenzenesulfonamide
The physical properties of N% 2CN + -dioxo-4-methylbenzaldehyde are quite important. This substance may be in a liquid state at room temperature, and it has a certain fluidity. It is like a smart water, but it has a unique quality. Its color state is often colorless to pale yellow, just like the morning light penetrating thin clouds, slightly yellowing, clear without losing depth.
Smell it, its smell is unique, with a fragrant charm, but it is also comparable to ordinary flowers. It is a special aroma of chemical substances, or it can play a role in the preparation of certain fragrances, adding a different flavor to it.
Furthermore, the density of this substance may be different from that of water. The state of its floating and sinking in water depends on the contrast of density. If the density is greater than that of water, it will sink to the bottom of the water, just like a pearl falling into a deep pool; if it is less than water, it will float on the water, like a light boat floating in blue waves.
The boiling point is also one of its key physical properties. When heated to a specific temperature, that is, the boiling point, N% 2CN + -dioxy-4-methylbenzaldehyde will change from liquid to gaseous state and turn into curling steam. This boiling point value is of great significance for the separation and purification of this substance. It can be precisely obtained from the mixture by distillation and other methods according to the difference in boiling point.
In terms of solubility, it varies in different solvents. In organic solvents, such as ethanol, ether, etc., or have good solubility, can blend with them, regardless of each other, as if water emulsion blends. In water, its solubility may be limited, only a little soluble, just like oil droplets entering water, it is difficult to completely miscible. This solubility characteristic is crucial for selecting suitable solvents to achieve specific chemical reactions or separation of substances in chemical experiments and industrial production.
Smell it, its smell is unique, with a fragrant charm, but it is also comparable to ordinary flowers. It is a special aroma of chemical substances, or it can play a role in the preparation of certain fragrances, adding a different flavor to it.
Furthermore, the density of this substance may be different from that of water. The state of its floating and sinking in water depends on the contrast of density. If the density is greater than that of water, it will sink to the bottom of the water, just like a pearl falling into a deep pool; if it is less than water, it will float on the water, like a light boat floating in blue waves.
The boiling point is also one of its key physical properties. When heated to a specific temperature, that is, the boiling point, N% 2CN + -dioxy-4-methylbenzaldehyde will change from liquid to gaseous state and turn into curling steam. This boiling point value is of great significance for the separation and purification of this substance. It can be precisely obtained from the mixture by distillation and other methods according to the difference in boiling point.
In terms of solubility, it varies in different solvents. In organic solvents, such as ethanol, ether, etc., or have good solubility, can blend with them, regardless of each other, as if water emulsion blends. In water, its solubility may be limited, only a little soluble, just like oil droplets entering water, it is difficult to completely miscible. This solubility characteristic is crucial for selecting suitable solvents to achieve specific chemical reactions or separation of substances in chemical experiments and industrial production.
What is the preparation method of N, N-dichloro-4-methylbenzenesulfonamide
Although there is no direct record of the specific expression "N% 2CN + - + dioxy + - + 4 + - + methylindole orange yellow" in "Tiangong Kaiwu", according to the traditional method of preparation and related chemical principles, it can be speculated that the method of preparing this product is as follows.
First of all, it is necessary to clarify the characteristics of the constituents of this product. Methylindole orange yellow or indole-related compounds, such compounds are often derived from the reaction of nitrogen-containing heterocycles. And the dioxy-related part, or refers to the introduction of a group containing dioxy atoms into the reaction.
If you want to prepare, first find a suitable starting material. Or you can choose to use the basic material of the indole structure, such as indole itself or its simple derivatives. These raw materials can be extracted from specific plants in nature, or synthesized from basic organic compounds through multi-step reactions.
For the introduction of methyl groups, halogenated methanes (such as iodomethane and bromomethane) are commonly reacted with indole derivatives containing active hydrogen under the catalysis of bases. The function of bases is to remove the active hydrogen of indole derivatives and generate carbon anions, which in turn undergo nucleophilic substitution reactions with halogenated methane and introduce methyl groups.
As for the dioxy part, it may be achieved by oxidation reaction. If the raw material contains suitable unsaturated bonds, such as carbon-carbon double bonds, suitable oxidizing agents can be selected, such as peroxides (hydrogen peroxide, m-chloroperoxybenzoic acid, etc.), the double bonds are epoxidized, and the dioxy ring structure is introduced.
During the reaction process, it is necessary to pay attention to the precise control of the reaction conditions. In terms of temperature, different reaction steps have different suitable temperatures. Introducing the nucleophilic substitution reaction of methyl groups may require appropriate heating to accelerate the reaction, but the temperature should not be too high to cause side reactions to occur. When the oxidation reaction introduces the dioxy structure, the temperature also needs to be precisely regulated to prevent excessive oxidation.
The choice of reaction solvent is also critical, to choose a solvent that has good solubility to the reactants and does not have adverse reactions with the reactants and products. For example, polar aprotic solvents such as N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO) can be selected for nucleophilic substitution reactions to promote ionic reactions.
To complete the reaction, separation and purification steps are required. The product can be extracted from the reaction system by extraction with a suitable organic solvent first, and then further purified by column chromatography and recrystallization to obtain a pure "N% 2CN + - + dioxy + - + 4 + - + methylindole orange yellow".
First of all, it is necessary to clarify the characteristics of the constituents of this product. Methylindole orange yellow or indole-related compounds, such compounds are often derived from the reaction of nitrogen-containing heterocycles. And the dioxy-related part, or refers to the introduction of a group containing dioxy atoms into the reaction.
If you want to prepare, first find a suitable starting material. Or you can choose to use the basic material of the indole structure, such as indole itself or its simple derivatives. These raw materials can be extracted from specific plants in nature, or synthesized from basic organic compounds through multi-step reactions.
For the introduction of methyl groups, halogenated methanes (such as iodomethane and bromomethane) are commonly reacted with indole derivatives containing active hydrogen under the catalysis of bases. The function of bases is to remove the active hydrogen of indole derivatives and generate carbon anions, which in turn undergo nucleophilic substitution reactions with halogenated methane and introduce methyl groups.
As for the dioxy part, it may be achieved by oxidation reaction. If the raw material contains suitable unsaturated bonds, such as carbon-carbon double bonds, suitable oxidizing agents can be selected, such as peroxides (hydrogen peroxide, m-chloroperoxybenzoic acid, etc.), the double bonds are epoxidized, and the dioxy ring structure is introduced.
During the reaction process, it is necessary to pay attention to the precise control of the reaction conditions. In terms of temperature, different reaction steps have different suitable temperatures. Introducing the nucleophilic substitution reaction of methyl groups may require appropriate heating to accelerate the reaction, but the temperature should not be too high to cause side reactions to occur. When the oxidation reaction introduces the dioxy structure, the temperature also needs to be precisely regulated to prevent excessive oxidation.
The choice of reaction solvent is also critical, to choose a solvent that has good solubility to the reactants and does not have adverse reactions with the reactants and products. For example, polar aprotic solvents such as N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO) can be selected for nucleophilic substitution reactions to promote ionic reactions.
To complete the reaction, separation and purification steps are required. The product can be extracted from the reaction system by extraction with a suitable organic solvent first, and then further purified by column chromatography and recrystallization to obtain a pure "N% 2CN + - + dioxy + - + 4 + - + methylindole orange yellow".
What are the precautions for the use of N, N-dichloro-4-methylbenzenesulfonamide?
There are many things to pay attention to during the use of Fu N% 2CN + -dioxy-4 -methylphenylthiazine blue.
First, it is related to environmental conditions. This agent should be stored in a place with suitable temperature and humidity, and should not be placed in a hot or humid place. High temperature can easily cause its properties to mutate, and humidity may cause the ingredients to be invaded, which affects the efficacy of the medicine. If placed in an open dew and heavy moisture place, it may become deliquescent in a few days and lose its original effect.
Second, the operation specification is very important. When taking it, be sure to use clean utensils and measure it accurately. If the utensils are unclean, impurities are mixed in, and the medicine is contaminated, it will be difficult to use it as expected. If the amount is not accurate, more may cause an overreaction, and less may cause insufficient efficacy. For example, when preparing a medicinal liquid, it needs to be taken quantitatively. If it is done casually, how can it be made into a medicine?
Third, safety protection should not be ignored. This medicine may have a certain impact on the human body. When operating, use protective equipment, such as gloves, masks, etc. If you accidentally touch the skin, rinse it with water immediately; if it enters the eye, you need to seek medical attention immediately. Do not cause damage to the body due to temporary convenience.
Fourth, the compatibility taboos must also be clear. Do not mix with some specific substances, otherwise it may cause adverse reactions. If it is unknown, it can be combined at will, for fear of accidental changes, endangering the safety of experiments or production.
In short, the use of N% 2CN + -dioxy-4 -methylbenzene thiazide blue, when it comes to the environment, operation, protection, compatibility, etc., should be paid attention to before it is correct.
First, it is related to environmental conditions. This agent should be stored in a place with suitable temperature and humidity, and should not be placed in a hot or humid place. High temperature can easily cause its properties to mutate, and humidity may cause the ingredients to be invaded, which affects the efficacy of the medicine. If placed in an open dew and heavy moisture place, it may become deliquescent in a few days and lose its original effect.
Second, the operation specification is very important. When taking it, be sure to use clean utensils and measure it accurately. If the utensils are unclean, impurities are mixed in, and the medicine is contaminated, it will be difficult to use it as expected. If the amount is not accurate, more may cause an overreaction, and less may cause insufficient efficacy. For example, when preparing a medicinal liquid, it needs to be taken quantitatively. If it is done casually, how can it be made into a medicine?
Third, safety protection should not be ignored. This medicine may have a certain impact on the human body. When operating, use protective equipment, such as gloves, masks, etc. If you accidentally touch the skin, rinse it with water immediately; if it enters the eye, you need to seek medical attention immediately. Do not cause damage to the body due to temporary convenience.
Fourth, the compatibility taboos must also be clear. Do not mix with some specific substances, otherwise it may cause adverse reactions. If it is unknown, it can be combined at will, for fear of accidental changes, endangering the safety of experiments or production.
In short, the use of N% 2CN + -dioxy-4 -methylbenzene thiazide blue, when it comes to the environment, operation, protection, compatibility, etc., should be paid attention to before it is correct.
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