Chemical Formula | C6H2Cl2F2O2S |
Molecular Weight | 259.04 |
Appearance | Typically a colorless to light - yellow liquid |
Boiling Point | Data may vary, usually in the range of high - boiling organic compounds |
Density | Specific value based on experimental determination for this sulfonyl chloride |
Solubility | Soluble in common organic solvents like dichloromethane, chloroform |
Pungency | Strongly pungent odor due to the sulfonyl chloride group |
Reactivity | Highly reactive towards nucleophiles, can undergo substitution reactions |
Hazard Class | Corrosive, harmful if inhaled, ingested or in contact with skin |
Chemical Formula | C6HCl2F2O2S |
Molecular Weight | 249.03 |
Appearance | Typically a colorless to pale - yellow liquid |
Physical State At Room Temp | Liquid |
Odor | Pungent, irritating odor |
Solubility In Water | Reacts with water |
Solubility In Organic Solvents | Soluble in many organic solvents like dichloromethane, toluene |
Boiling Point | Estimated to be in a certain range (experimental determination needed) |
Density | Experimental determination needed, but likely higher than water |
Hazard Class | Corrosive, can cause severe burns to skin and eyes |
Chemical Formula | C6HCl2F2O2S |
Molecular Weight | 259.036 |
Appearance | Typically a colorless to light - colored liquid or solid |
Physical State | At room temperature, may be a liquid or solid depending on purity and conditions |
Odor | Pungent, characteristic of sulfonyl chloride compounds |
Solubility | Soluble in many organic solvents like dichloromethane, chloroform |
Boiling Point | Approximately [specific value if known] °C (decomposes in some cases) |
Melting Point | Approximately [specific value if known] °C |
Density | [Value] g/cm³ |
Reactivity | Highly reactive, reacts with water, alcohols, amines |
Hazard Class | Corrosive, causes burns to skin, eyes and respiratory tract |
What are the main uses of 2-Chloro-4, 6-difluorobenzenesulfonyl chloride?
2-Chloro-4,6-difluorobenzenesulfonyl chloride is a crucial chemical raw material in the field of organic synthesis. It has a wide range of uses and is often used as a key intermediate in medicinal chemistry to help synthesize a variety of specific drugs. Due to the unique structure of the compound, containing special atoms such as chlorine and fluorine, it can precisely construct a drug active molecular structure through organic chemical reactions. For example, it is used to synthesize antibacterial and antiviral drugs. Its special structure and bacterial action inhibit or kill bacteria for therapeutic purposes.
In the field of pesticide chemistry, 2-chloro-4,6-difluorobenzenesulfonyl chloride also plays a pivotal role. It can be used to create new types of pesticides, and by virtue of its structural characteristics, it can give pesticides unique biological activities, such as high selective toxicity to specific pests, or can regulate plant growth, improve crop yield and quality, and some pesticides also have high stability and environmental friendliness due to fluorine atoms.
Furthermore, in the field of materials science, it is also useful. Polymer structures can be introduced through chemical reactions to improve material properties, such as improving material chemical stability, heat resistance, weather resistance, etc. Materials treated in this way may be used in aerospace, automobile manufacturing and other fields that require strict material properties to meet special environmental needs. Overall, the unique structure of 2-chloro-4,6-difluorobenzenesulfonyl chloride plays an indispensable role in many fields such as medicine, pesticides, and materials, providing key support for the development of various fields.
What are the physical properties of 2-Chloro-4, 6-difluorobenzenesulfonyl chloride
2-Chloro-4,6-difluorobenzenesulfonyl chloride is an important compound in organic chemistry. Its physical properties are particularly important and are related to many practical applications.
When it comes to its properties, under normal temperature and pressure, the substance is mostly colorless to light yellow liquid. Looking at its color, or slightly different due to some impurities, pure people often show this color. The appearance of its liquid form suggests that its intermolecular forces are in a specific range, making it a mobile phase under normal conditions.
Furthermore, the boiling point is also one of the key physical properties. At a certain temperature, 2-chloro-4,6-difluorobenzenesulfonyl chloride will change from a liquid state to a gaseous state. This boiling point value reflects the strength of molecular interactions, such as van der Waals forces, hydrogen bonds, etc. The exact value of the boiling point provides an important basis for practical operations such as distillation and purification.
The melting point should not be underestimated. Although it is a liquid at room temperature, it will solidify when cooled to a certain temperature. The determination of the melting point helps to understand its solid structure and molecular arrangement. When the temperature drops below the melting point, the molecular activities are limited and close to each other, forming a regular lattice structure.
Density is also an important consideration. The mass of the substance contained in a unit volume reflects the compactness of its molecules. The density of 2-chloro-4,6-difluorobenzenesulfonyl chloride is specific, and this parameter is indispensable when it comes to mixing, separation, etc. Substances of different densities can be layered or uniformly mixed in liquid systems, depending on the density difference.
The solubility is also significant. In organic solvents, such as some halogenated hydrocarbons, aromatics, etc., it often exhibits good solubility. Due to the principle of similar miscibility, its molecular structure is similar to that of organic solvents. In water, because the molecular polarity does not exactly match the water molecule, the solubility is poor. This difference in solubility has far-reaching effects on chemical synthesis, product separation, and environmental behavior.
In summary, the physical properties of 2-chloro-4,6-difluorobenzenesulfonyl chloride, such as its properties, boiling point, melting point, density, solubility, etc., are of great significance to its research and application in the field of chemistry, providing a solid foundation for synthesis, analysis and practical production operations.
What are the chemical properties of 2-Chloro-4, 6-difluorobenzenesulfonyl chloride?
2-Chloro-4,6-difluorobenzenesulfonyl chloride is one of the most characteristic organic compounds. It is active and plays an important role in many organic synthesis reactions.
This compound has strong reactivity, due to the sulfonyl chloride group (-SO 2O Cl). In this group, the sulfur atom has high positive electricity, and the chlorine atom is easy to leave, so the compound is easy to react with nucleophilic reagents. Nucleophilic reagents such as alcohols and amines can react with the chlorine atom in 2-chloro-4,6-difluorobenzenesulfonyl chloride to form corresponding sulfonates or sulfonamides. This property is widely used in drug synthesis, materials science and other fields, and can be used to construct organic molecules with diverse structures.
Furthermore, the chlorine and fluorine atoms on the benzene ring also affect its chemical properties. The high electronegativity of fluorine atoms can reduce the electron cloud density of the benzene ring, which in turn affects the activity and selectivity of nucleophilic substitution reactions. At the same time, the existence of these halogen atoms also endows the compound with a certain lipid solubility, which is of great significance in some application scenarios that require specific physical and chemical properties.
2-chloro-4,6-difluorobenzenesulfonyl chloride is more sensitive to water and air. When exposed to water, the sulfonyl chloride group is prone to hydrolysis, forming sulfonic acid and hydrogen chloride. In the air, it may also gradually hydrolyze and deteriorate due to factors such as humidity. Therefore, when storing and using, it needs to be properly protected to isolate water vapor and air to ensure its chemical stability and reactivity.
In summary, 2-chloro-4,6-difluorobenzenesulfonyl chloride has great potential in the field of organic synthesis due to its unique structure and active chemical properties. However, when using and preserving, it is also necessary to pay attention to its special requirements.
What is the preparation method of 2-Chloro-4, 6-difluorobenzenesulfonyl chloride?
The method of preparing 2-chloro-4,6-difluorobenzenesulfonyl chloride followed a specific chemical path in the past. The method is as follows:
First, 2-chloro-4,6-difluoroaniline is used as the starting material. First, 2-chloro-4,6-difluoroaniline is reacted with nitrosyl sulfuric acid in a low temperature and finely regulated environment. Nitrosyl sulfuric acid needs to be added slowly, and the temperature of the reaction system should be maintained at a suitable range. Because the temperature is too high, it is easy to cause side reactions to cluster, which affects the purity and yield of the product. This step of the reaction produces a diazonium salt intermediate, which has high chemical activity.
Then, the resulting diazonium salt intermediate is reacted with potassium thiocyanate. This reaction needs to be carried out in a suitable solvent, and the choice of solvent is crucial to enable the reactants to dissolve sufficiently without additional side reactions with the reactants and products. During the reaction, the reaction process needs to be closely monitored, and the extent of the reaction can be determined by means such as thin layer chromatography. This step generates 2-chloro-4,6-difluorobenzene thiocyanate.
Subsequently, 2-chloro-4,6-difluorobenzene thiocyanate is hydrolyzed under specific conditions. The reagents and reaction conditions used in hydrolysis need to be strictly controlled. Generally, an appropriate concentration of acid or base is used as the hydrolysis reagent, heated to an appropriate temperature, and the thiocyanate group is gradually converted into a sulfonyl chloride group.
After hydrolysis is completed, the product still contains impurities and needs to go through a series of purification steps. Common methods are distillation, recrystallization, etc. During distillation, the temperature and pressure are precisely controlled according to the difference between the boiling point of the product and the impurity to separate the pure 2-chloro-4,6-difluorobenzenesulfonyl chloride. Recrystallization requires the selection of a suitable solvent to fully dissolve the product in a hot solvent, and slowly precipitate after cooling to obtain a high-purity crystal product.
There is another method, using 2-chloro-4,6-difluorobenzene as the starting material, the sulfonic acid group is first introduced through a sulfonation reaction, and then the sulfonic acid group is converted into a sulfonyl chloride group by a chlorination reagent. In the sulfonation reaction, a strong sulfonating reagent such as fuming sulfuric acid is selected, and the reaction conditions also need to be carefully adjusted to ensure the precise positioning of the sulfonic acid group. The chlorination reagents used in the chlorination step, such as phosphorus pentachloride, dichlorosulfoxide, etc., should be paid attention to during the reaction, the amount and the reaction temperature, time and other factors to avoid excessive chlorination or incomplete reaction. Subsequent purification operations are also required to obtain a pure target product 2-chloro-4,
What are the precautions for storage and transportation of 2-Chloro-4, 6-difluorobenzenesulfonyl chloride?
2-Chloro-4,6-difluorobenzenesulfonyl chloride is a chemical substance. When storing and transporting, you need to pay more attention to the following things.
One is the importance of storage. This substance should be placed in a cool, dry and well-ventilated place. Because of its chemical activity, high temperature and humid environment are prone to deterioration or dangerous reactions. Therefore, the warehouse temperature should be controlled within a suitable range and should not be too high. And it needs to be kept away from fire and heat sources. Open flames are close, and there is a fear of accidents. This substance may be corrosive and should be stored separately from alkalis and alcohols. Do not mix storage to prevent interaction and lead to accidents.
The second is related to transportation regulations. Before transportation, it is necessary to ensure that the packaging is complete and sealed. The packaging material needs to be able to resist its corrosiveness and not leak. During transportation, the driving should be stable to avoid bumps and shocks to prevent package damage. Transportation vehicles should also be equipped with corresponding varieties and quantities of fire-fighting equipment and leakage emergency treatment equipment. If there is a leak on the way, do not panic, and should be dealt with according to the established emergency plan. Operators need professional protective equipment to avoid direct contact with leaks.
Furthermore, whether it is storage or transportation, special personnel need to manage and record. Detailed records of warehousing time, quantity, storage and transportation status. Periodically inspect the storage environment and transportation equipment to detect and deal with potential hazards in a timely manner, so as to ensure the safety of 2-chloro-4,6-difluorobenzenesulfonyl chloride during storage and transportation.