Chemical Formula | C6H2Cl2F2O2S |
Molar Mass | 259.046 g/mol |
Appearance | Solid (likely white or off - white) |
Physical State At Room Temperature | Solid |
Solubility In Water | Reacts with water rather than dissolves (hydrolyzes to form sulfuric acid, hydrochloric acid and a phenolic derivative) |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, chloroform, etc. |
Reactivity | Highly reactive, reacts with nucleophiles such as amines, alcohols, and water |
Chemical Formula | C6H2Cl2F2O2S |
Molecular Weight | 259.046 |
Appearance | Typically a solid, appearance can vary based on purity and preparation |
Solubility | Soluble in certain organic solvents like dichloromethane, chloroform, etc., but details vary |
Chemical Formula | C6H2Cl2F2O2S |
Molar Mass | 247.047 g/mol |
Appearance | Solid (usually) |
Physical State At Room Temp | Solid |
Color | Typically colorless to light - colored |
Odor | Pungent, characteristic of sulfonyl chloride |
Solubility In Water | Reacts with water |
Solubility In Organic Solvents | Soluble in many organic solvents like dichloromethane, chloroform |
Boiling Point | Data may vary, but relatively high due to polar groups |
Melting Point | Specific value would need experimental determination |
Reactivity | Highly reactive, especially towards nucleophiles |
Hazard Class | Corrosive, toxic |
5-CHLORO-2, 4-DIFLUOROBENZENESULPHONYL what is the main use of CHLORIDE
5-Chloro-2,4-difluorobenzenesulfonyl chloride is a crucial chemical raw material in organic synthesis. It has a wide range of uses and can be used as a key intermediate in the field of pharmaceutical synthesis. It participates in the construction of many drug molecules. Gein benzenesulfonyl chloride groups have active chemical properties and can react with a variety of nucleophiles containing nitrogen and oxygen. By ingeniously designing the reaction path, various drugs with complex structures can be precisely prepared.
In the creation of pesticides, 5-chloro-2,4-difluorobenzenesulfonyl chloride also plays an important role. After chemical transformation, compounds with high insecticidal, bactericidal or herbicidal activities can be derived. This is because the structural characteristics of the substance give it the ability to combine with specific targets in the organism, thereby interfering with the normal physiological activities of the organism and achieving the purpose of preventing harmful organisms.
In addition, in the field of materials science, it can be used to prepare polymer materials with special functions. For example, by polymerizing with monomers containing unsaturated bonds, the structure of benzenesulfonyl chloride can be introduced into the main chain or side chain of the polymer, giving the material unique properties such as antistatic and chemical corrosion resistance, and expanding the application scenarios of the material.
Furthermore, in the preparation of fine chemical products, 5-chloro-2,4-difluorobenzenesulfonyl chloride can be used to synthesize special surfactants, dye additives, etc. Its unique structure can improve the physical and chemical properties of the product, such as solubility and dispersion, and improve product quality and performance. In short, 5-chloro-2,4-difluorobenzenesulfonyl chloride has shown indispensable and important uses in many fields due to its unique chemical structure and active reactivity.
5-CHLORO-2, 4-DIFLUOROBENZENESULPHONYL the physical properties of CHLORIDE
5-Chloro-2,4-difluorobenzenesulfonyl chloride is an important compound in organic chemistry. Its physical properties are quite unique and are described below.
Looking at its properties, under normal temperature and pressure, 5-chloro-2,4-difluorobenzenesulfonyl chloride is mostly colorless to pale yellow liquid. The characterization of this color state can be used as a basis for preliminary identification in chemical experiments and industrial production.
When it comes to the melting point, the melting point of this compound is relatively low. This property makes it easier to change from solid to liquid at a specific temperature environment, showing good phase transition properties.
In terms of boiling point, its boiling point is within a certain range, which is of great significance for the separation and purification of compounds. In separation processes such as distillation, 5-chloro-2,4-difluorobenzenesulfonyl chloride can be effectively separated from the mixture according to its boiling point characteristics.
Furthermore, the density of 5-chloro-2,4-difluorobenzenesulfonyl chloride is also a key physical property. Its density determines the distribution of this substance and other substances in the mixed system, and plays an indispensable role in liquid-liquid extraction and other processes.
Solubility is also one of its important physical properties. This compound exhibits a certain solubility in some organic solvents, such as common toluene, dichloromethane and other organic solvents, in which 5-chloro-2,4-difluorobenzenesulfonyl chloride can be dissolved. This property provides convenient conditions for its participation in various organic synthesis reactions, so that the reactants can contact and react more fully.
In addition, 5-chloro-2,4-difluorobenzenesulfonyl chloride has a certain volatility, and in the open system, it will gradually evaporate to the surrounding environment. Its volatilization rate is affected by many factors such as temperature and pressure.
In summary, the physical properties of 5-chloro-2,4-difluorobenzenesulfonyl chloride, such as color state, melting point, boiling point, density, solubility, and volatility, are interrelated and meaningful, providing a foundation for its application in many fields such as organic synthesis and chemical production.
5-CHLORO-2, 4-DIFLUOROBENZENESULPHONYL the chemical properties of CHLORIDE
5-Chloro-2,4-difluorobenzenesulfonyl chloride, this is an organic compound with unique chemical properties.
This compound contains halogen atoms such as chlorine and fluorine, and the existence of halogen atoms endows it with many characteristics. Chlorine and fluorine atoms have high electronegativity, which can cause uneven distribution of molecular charges, resulting in a certain polarity. Because of its polarity, it may be soluble in some polar solvents and can participate in a variety of polar-related reactions.
Its sulfonyl chloride group (-SO 2O Cl) is extremely active. When exposed to water, it is prone to hydrolysis reaction, and the sulfonyl chloride group will react with water to form the corresponding sulfonic acid (-SOH) and hydrogen chloride (HCl). This hydrolysis reaction is more violent, and hydrogen chloride escapes, or the acidity of the reaction system is enhanced.
In the field of organic synthesis, sulfonyl chloride groups are often used as important intermediates. It can react with alcohols to form sulfonates. During this reaction, the chlorine atoms of sulfonyl chloride are replaced by alkoxy groups of alcohols to form sulfonate esters with diverse structures. Such compounds are widely used in materials science, pharmaceutical chemistry and other fields.
At the same time, the halogen atoms in this compound can participate in nucleophilic substitution reactions. Nucleophilic reagents can attack the carbon atoms connected to the halogen atoms, and the halogen atoms leave to realize the transformation of molecular structures, providing an effective path for the synthesis of complex organic molecules.
Furthermore, due to the special electronic effect of fluorine atoms, it can enhance the stability of molecules and affect their physical and chemical properties, such as changing the boiling point and melting point of compounds. In drug development, the introduction of fluorine atoms can often optimize the biological activity and metabolic stability of drug molecules. In short, 5-chloro-2,4-difluorobenzenesulfonyl chloride plays a key role in many fields such as organic synthesis due to its unique chemical properties.
5-CHLORO-2, 4-DIFLUOROBENZENESULPHONYL what is the production method of CHLORIDE
The preparation method of 5-chloro-2,4-difluorobenzenesulfonyl chloride has been in place since ancient times, but the production method may be more advanced today. The traditional production method often follows the following methods.
First take the appropriate raw materials containing chlorine, fluorine and benzene rings. This raw material needs to have a specific structure to meet the needs of subsequent reactions. In a specific reaction vessel, add an appropriate amount of reactants, and carefully prepare the reaction environment, such as temperature, pressure, reaction medium, etc., all need to be strictly controlled. The temperature is related to the rate of reaction and the purity of the product, and the pressure is also the same. The reaction medium provides a suitable place for the reaction to occur, which can affect the direction and process of the reaction. < Br >
At the beginning of the reaction, a specific catalyst may be required to intervene to speed up the reaction rate and reduce the activation energy required for the reaction. The choice of this catalyst is crucial and depends on the characteristics of the raw materials and the mechanism of the reaction. When the reaction is in progress, the process of the reaction can be closely monitored. Various analytical methods, such as chromatographic analysis, spectral analysis, etc., can be used to gain insight into the changes of various substances in the reaction system and adjust the reaction conditions in a timely manner.
After the reaction is completed asymptotically, the product may contain impurities, so separation and purification operations are required. The target product 5-chloro-2,4-difluorobenzenesulfonyl chloride can be precisely separated from the reaction mixture by distillation, extraction, crystallization, etc., to improve its purity and meet the required Quality Standards. At present, there are many innovations in the production method, or in the selection of raw materials, the optimization of reaction conditions, the improvement of catalysts, and the refinement of separation and purification technologies, so as to increase the yield and quality of the product. However, the basic principle does not deviate from the above traditional method.
What are the precautions for 5-CHLORO-2, 4-DIFLUOROBENZENESULPHONYL CHLORIDE in storage and transportation?
5-Chloro-2,4-difluorobenzenesulfonyl chloride is a chemical substance, and many things must be paid attention to when storing and transporting it.
Let's talk about storage first. This chemical is active in nature and should be stored in a cool, dry and well-ventilated place. It must not be placed in a high temperature place, because high temperature can easily cause it to react, or there is a risk of decomposition, which may cause danger. And it should be kept away from fires and heat sources, and avoid direct sunlight to prevent it from deteriorating due to light. In addition, it should be stored separately from oxidants and alkalis, and must not be mixed. Because it encounters with these substances, it may react violently, resulting in accidents. In the warehouse, suitable materials should also be prepared to contain leaks to prevent accidents.
As for transportation. Before transportation, it is necessary to ensure that the packaging is complete and sealed. The packaging material must be strong and can withstand a certain pressure to prevent leakage due to package damage during transportation. During transportation, the prescribed route should be strictly followed and cannot be changed at will. Drivers and escorts must have professional knowledge and be familiar with the characteristics of the chemical and emergency treatment methods. Transportation vehicles should also be equipped with corresponding fire fighting equipment and leakage emergency treatment equipment. In case of emergency, they can respond in time. And during transportation, pay close attention to environmental factors such as temperature and humidity to avoid adverse consequences due to environmental discomfort. In this way, the safety of 5-chloro-2,4-difluorobenzenesulfonyl chloride during storage and transportation can be ensured.