4 Fluorobenzenesulphonyl Chloride
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
4-fluorobenzenesulphonyl chloride
Chemical Formula C6H4ClFO2S
Molecular Weight 196.61
Appearance Colorless to light yellow liquid
Boiling Point Around 230 - 232 °C
Density Approx. 1.52 g/cm³
Solubility Reacts with water, soluble in many organic solvents
Vapor Pressure Low vapor pressure at room temperature
Flash Point High, likely above 100 °C
Stability Reactive, especially with water and nucleophiles
Name 4-fluorobenzenesulphonyl chloride
Chemical Formula C6H4ClFO2S
Molar Mass 194.61 g/mol
Appearance Colorless to light yellow liquid
Boiling Point 110 - 112 °C at 15 mmHg
Melting Point 21 - 23 °C
Density 1.486 g/cm³
Solubility Reacts with water, soluble in organic solvents like dichloromethane
Pungency Has a pungent odor
Reactivity Reactive towards nucleophiles, can form sulfonamides, esters etc.
Chemical Formula C6H4ClFO2S
Molecular Weight 194.61
Appearance Colorless to pale yellow liquid
Boiling Point 224 - 226 °C
Melting Point N/A
Density 1.48 g/cm³
Solubility Reacts with water, soluble in organic solvents
Flash Point 101.7 °C
Refractive Index 1.534 - 1.536
Stability Stable under normal conditions, but reactive with water and bases
Odor Pungent
FAQ

What are the main uses of 4-fluorobenzenesulphonyl chloride?

4-Fluorobenzenesulfonyl chloride is an important agent in organic synthesis. Its main uses are briefly described as follows.

In the field of pharmaceutical synthesis, its function is quite significant. It can be used as a key intermediate to produce a variety of drugs. For example, some compounds with specific pharmacological activities, through the reaction of 4-fluorobenzenesulfonyl chloride, a fluorobenzenesulfonyl group is introduced. This group may change the physical, chemical properties and biological activities of the compound, and improve the affinity and selectivity of the drug to specific targets. It is widely used in the creation of antibacterial, anti-inflammatory, anti-tumor and other drugs.

In the synthesis of pesticides, it is also indispensable. The structure constructed by it can endow pesticides with unique properties. Such as enhancing the efficacy of pesticides on pests, stomach toxicity, or improving their stability and sustainability in the environment, it will help to develop high-efficiency, low-toxicity and environmentally friendly new pesticides to protect agricultural production and reduce pest damage.

In the field of materials science, 4-fluorobenzenesulfonyl chloride can also be used. In the preparation of polymers, if this structure is introduced, the properties of polymers can be changed. For example, to improve its thermal stability, mechanical properties or chemical stability, etc., making it suitable for more severe conditions, it has made great contributions to the research and development of high-performance engineering plastics, special fibers and other materials.

Furthermore, in the field of dye synthesis, 4-fluorobenzenesulfonyl chloride can be used as a raw material to participate in the construction of dye molecules. By introducing special groups, or adjusting the color and fastness of dyes, high-quality dyes with bright color, light resistance and washable properties are prepared, which are widely used in textile printing and dyeing industries.

In short, 4-fluorobenzenesulfonyl chloride is an important synthetic raw material in many fields such as medicine, pesticides, materials, dyes, etc., promoting the development and progress of various industries.

What are the physical properties of 4-fluorobenzenesulphonyl chloride?

4-Fluorobenzenesulfonyl chloride, this material has many physical properties. Its appearance is colorless to light yellow liquid, and it is stable under room temperature and pressure. Looking at its color, it is almost colorless when pure, but it may be slightly yellow due to impurities.

Smell it, there is a pungent smell, this smell is strong and irritating, and it is easy to make the nasal cavity and throat uncomfortable. Its boiling point is in a specific range, about [specific value] ℃. At this temperature, the liquid will gradually change to a gaseous state. The melting point is around [specific value] ℃, below this temperature, the substance will change from liquid to solid state.

The density of 4-fluorobenzenesulfonyl chloride is also an important physical property. Compared with water, its density is slightly higher, about [specific value] g/cm ³. The solubility in water is not good. Due to its molecular structure characteristics, the interaction with water is weak. When the two are mixed, there will be stratification, and 4-fluorobenzenesulfonyl chloride sinks to the bottom.

In addition, the volatility of this substance cannot be ignored. Although the volatilization rate is not very fast at room temperature, in poor ventilation, its volatilized gas will gradually accumulate, causing the concentration in the air to rise, increasing the danger. These physical properties need to be carefully considered in the production, storage and transportation of chemical industry to prevent the occurrence of harmful accidents.

Is 4-fluorobenzenesulphonyl chloride chemically stable?

The chemical stability of 4-fluorobenzenesulfonyl chloride is related to many aspects. This substance has active chemical properties and is not very stable.

Looking at its structure, the fluorine atom is connected to the benzene ring. Due to the strong electronegativity of fluorine, it has a significant impact on the electron cloud distribution of the benzene ring, which can cause the electron cloud density of the benzene ring to decrease. And the sulfonyl chloride group (-SO ² Cl) is also an active functional group.

When exposed to water, 4-fluorobenzenesulfonyl chloride is prone to hydrolysis. The chlorine atom in the sulfonyl chloride group is attacked by water, and the chlorine is replaced by a hydroxyl group, resulting in 4-fluorobenzenesulfonic acid and hydrogen chloride. Its reaction is rapid, and the sulfur-chlorine bond in the sulfonyl chloride group has a certain polarity, which is easy to be broken by nucleophilic reagents.

Under heat or light conditions, 4-fluorobenzenesulfonyl chloride is also unstable. When heated, the intra-molecular energy increases, which can cause the breaking and rearrangement of chemical bonds such as sulfur-chlorine bonds and carbon-fluorine bonds, triggering complex chemical reactions. Light can cause molecular excitation, which prompts reactions, such as free radical reactions.

4-fluorobenzenesulfonyl chloride meets alkali and reacts quickly. The hydroxide ion in the base has strong nucleophilicity, which will attack the sulfur atom of the sulfonyl chloride group, generate the corresponding sulfonate, and release chloride ions at the same time.

In summary, 4-fluorobenzenesulfonyl chloride is chemically active and has poor stability due to the active functional groups in the structure. When storing and using, it is necessary to pay attention to conditions such as waterproofing, temperature control, and light protection to ensure the relative stability of its chemical properties and prevent the occurrence of adverse reactions.

What are the synthetic methods of 4-fluorobenzenesulphonyl chloride?

There are several common methods for synthesizing 4-fluorobenzenesulfonyl chloride.

First, 4-fluorobenzene sulfonate is prepared by sulfonation of 4-fluorobenzene as a starting material, and then reacts with chlorination reagents. First, 4-fluorobenzene is co-heated with concentrated sulfuric acid. In this process, the sulfuric acid group (-SO 🥰 H) replaces the hydrogen on the benzene ring to generate 4-fluorobenzene sulfonic acid. Subsequently, the obtained 4-fluorobenzene sulfonic acid is reacted with chlorinated reagents such as phosphorus pentachloride and phosphorus oxychloride, and the hydroxyl group of the sulfonic acid group is replaced by a chlorine atom to obtain 4-fluorobenzene sulfonyl The reaction process is relatively clear, but it is necessary to pay attention to the reaction temperature and reagent dosage during operation to avoid side reactions.

Second, 4-fluoroaniline can be used. First, 4-fluoroaniline is diazotized, and 4-fluoroaniline is treated with sodium nitrite and hydrochloric acid at low temperature to form diazonium salts. Then, the diazonium salt interacts with sodium bisulfite and copper sulfate to form 4-fluorobenzenesulfonate, and then acidifies to obtain 4-fluorobenzenesulfonic acid. Finally, 4-fluorobenzenesulfonyl chloride is obtained by reacting with chlorination reagents as before. This approach is slightly complicated, but it can precisely control the reaction check point and reduce the generation of impur

Third, 4-fluorobenzoyl chloride is used as raw material. First, 4-fluorobenzoyl chloride is converted into the corresponding sulfinite, and then oxidized and chlorinated. Sodium 4-fluorobenzenesulfite can be formed by reacting with sodium sulfite, and then treated with chlorine and other oxidants to realize the conversion of sulfinite to sulfonyl chloride. This method needs to pay attention to the control of oxidation conditions to prevent side reactions such as excessive oxidation.

The above synthesis methods have their own advantages and disadvantages. In practical application, the appropriate method should be weighed according to factors such as the availability of raw materials, the ease of control of reaction conditions, and the requirements of product purity.

What are the precautions for 4-fluorobenzenesulphonyl chloride in storage and transportation?

4-Fluorobenzenesulfonyl chloride is a very important class of chemical substances. When storing and transporting, there are many key things to pay attention to.

First, storage, because of its corrosive and chemical activity, must choose a dry, cool and well-ventilated place. If stored in a humid place, it may react with water vapor, causing deterioration and damaging its chemical properties. In addition, the temperature also needs to be strictly controlled. High temperature can easily promote its decomposition or accelerate chemical reactions, so it is better to be at a suitable low temperature. And it should be kept away from fire and heat sources, because it may be flammable or the risk of heat reaction, otherwise it is prone to fire and explosion.

Second, transportation requires strict regulations for chemical transportation. The containers used must be resistant to corrosion and pressure to ensure that there is no leakage during transportation. When loading and unloading, operators should operate with caution and wear appropriate protective equipment, such as chemical protective clothing, gloves, goggles, etc., to prevent them from coming into contact with the skin and eyes, causing burns and other injuries. Transportation vehicles also need to be specially prepared and have corresponding warning signs indicating that they are carrying dangerous chemicals to alert passers-by. At the same time, transportation route planning also needs to be careful to avoid sensitive areas such as crowded areas and water source reserves. If there is a leak, it can reduce its harm.

Furthermore, whether it is storage or transportation, it is necessary to record its quantity, warehousing time, transportation track and other information in detail for traceability and supervision. If an accident occurs, it can be quickly responded to. All these precautions are to ensure the safety of 4-fluorobenzenesulfonyl chloride storage and transportation, to avoid accidents, to protect personnel safety and the safety of the environment.