Chemical Formula | C6H3Cl2FO2S |
Molar Mass | 231.056 g/mol |
Appearance | Typically a colorless to light - yellow liquid |
Density | data needed |
Boiling Point | data needed |
Melting Point | data needed |
Solubility | Soluble in common organic solvents like dichloromethane, chloroform |
Flash Point | data needed |
Vapor Pressure | data needed |
Reactivity | Reactive towards nucleophiles due to the presence of sulfonyl chloride group |
Chemical Formula | C6H3Cl2FO2S |
Molar Mass | 231.056 g/mol |
Appearance | Typically a colorless to light - yellow liquid |
Density | Data depends on temperature, usually around 1.6 - 1.7 g/cm³ |
Boiling Point | Around 270 - 280 °C (decomposes in some cases) |
Solubility | Soluble in many organic solvents like dichloromethane, chloroform |
Vapor Pressure | Low vapor pressure at room temperature |
Stability | Reactive, especially towards nucleophiles |
Odor | Pungent, characteristic sulfonyl chloride odor |
Chemical Formula | C6H3Cl2FO2S |
Molar Mass | 231.056 g/mol |
Appearance | Solid (usually) |
Physical State At Room Temp | Solid |
Color | Typically white to off - white |
Odor | Pungent, irritating odor |
Solubility In Water | Reacts with water |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, chloroform |
What are the main uses of 3-Chloro-4-Fluorobenzene-1-Sulfonyl Chloride?
3-Chloro-4-fluorobenzene-1-sulfonyl chloride, an organic compound, is widely used in the chemical industry, medicine and other fields.
In the chemical industry, it is often used as a key intermediate. In many organic synthesis reactions, with its unique chemical structure, chlorine, fluorine and sulfonyl chloride groups can be introduced. For example, in the synthesis of complex aromatic compounds, these groups can participate in various reactions such as nucleophilic substitution and electrophilic substitution, thereby forming the desired carbon-carbon bond and carbon-heteroatomic bond to achieve the synthesis of the target compound. In the preparation of special polymer materials, it can be used as a polymeric monomer or modifier to endow polymer materials with specific properties such as chemical resistance and heat resistance.
In the field of medicine, its position is also crucial. In many drug molecule designs, it is used as an important starting material. Through subsequent reaction modification, its structure is integrated into the active ingredient of the drug, and the characteristics of chlorine, fluorine atom and sulfonyl chloride group change the fat solubility, water solubility and interaction ability of the drug molecule with biological targets, thereby improving the drug efficacy and reducing toxic and side effects. For example, in the development of some new antibacterial drugs, it is used to construct key pharmacoactive groups to enhance the inhibition and killing effect of the drug on specific bacteria. 3-Chloro-4-fluorobenzene-1-sulfonyl chloride plays an irreplaceable role in many fields due to its special chemical properties, promoting the development and innovation of related industries.
What are the physical properties of 3-Chloro-4-Fluorobenzene-1-Sulfonyl Chloride?
3-Chloro-4-fluorobenzene-1-sulfonyl chloride is one of the organic compounds. Its physical properties are crucial and are related to many chemical applications.
Looking at its properties, under normal temperature and pressure, this substance is often in the form of a colorless to light yellow liquid, and it can be seen in sunlight. It is clear and has a specific luster. This is a characteristic that can be seen intuitively by the naked eye.
When it comes to boiling point, it is about a specific temperature range. This value is very important in chemical experiments and industrial production in distillation, separation and other operations. It can be used to control the reaction conditions and make the separation and purification of substances meet expectations.
Its melting point also has a certain value, which is of great significance in the study of phase transition and solid storage of substances. When the temperature drops below the melting point, the compound will gradually change from liquid to solid state, and the change of morphology is accompanied by many physical properties.
Furthermore, density is also one of the important physical properties. The value of its density reflects the mass of the substance per unit volume. During solution preparation and mixing, the density parameter can help chemists accurately calculate the dosage of each substance and ensure that the chemical reaction proceeds in the expected direction.
In terms of solubility, 3-chloro-4-fluorobenzene-1-sulfonyl chloride exhibits specific solubility in common organic solvents. In some organic solvents such as dichloromethane and chloroform, it can exhibit good solubility. This property provides convenience for organic synthesis reactions. Because many organic reactions need to be carried out in a solution environment, the appropriate solubility can make the reactants fully contact, accelerate the reaction process, and improve the reaction efficiency.
In addition, its volatility cannot be ignored. Moderate volatility
means that the substance can change from liquid to gaseous under certain conditions. This property is very important in the consideration of ventilation and storage conditions. It needs to be treated with caution to prevent material loss due to volatilization or potential safety hazards.
In summary, the physical properties of 3-chloro-4-fluorobenzene-1-sulfonyl chloride are diverse and have their own uses. They play an important role in the research and production practice of the chemical field. Chemists need to understand their properties in detail in order to make good use of them and promote the development of the chemical industry.
What are the synthesis methods of 3-Chloro-4-Fluorobenzene-1-Sulfonyl Chloride?
The synthesis method of 3-chloro-4-fluorobenzene-1-sulfonyl chloride has been recorded in various books throughout the ages. Now let's come to you one by one.
First, it can start from the corresponding aromatic hydrocarbons. Using 3-chloro-4-fluorobenzene as raw material, first use a sulfonating agent such as fuming sulfuric acid, and react carefully at a suitable temperature to obtain 3-chloro-4-fluorobenzene sulfonic acid. In this step, temperature control is crucial. If the temperature is high, side reactions will occur; if the temperature is low, the reaction will be slow and the yield will be poor. Then, the sulfonic acid is treated with a chlorinating agent, such as phosphorus pentachloride or sulfoxide dichloride. When chlorinating, it is necessary to pay attention to the anhydrous environment of the reaction system. Otherwise, the chlorinating agent is easy to hydrolyze and the reaction does not meet expectations. In this way, 3-chloro-4-fluorobenzene-1-sulfonyl chloride can be obtained.
Second, there are also derivatives of halogenated aromatics as starters. If a halobenzene derivative containing a specific substituent is used, a sulfonyl group is introduced first. This may require the help of specific catalysts and reaction conditions to create an environment conducive to the introduction of sulfonyl groups. Then, through the halogenation step, chlorine atoms and fluorine atoms are precisely introduced at a predetermined position. This path requires careful consideration of the selectivity of each step of the reaction, so that the transformation of functional groups occurs as expected without side branches.
Third, there is a method that uses the electrophilic substitution reaction on the aromatic ring. Select the appropriate aromatic ring substrate, use the reagent with sulfonyl chloride and halogen atom, and perform electrophilic substitution under the catalysis of Lewis acid and other catalysts. In this process, the choice of catalyst, the activity of the substrate and the reaction medium all have a profound impact on the reaction process and the purity and yield of the product. Fine regulation is required to make the reaction smooth and obtain high-purity 3-chloro-4-fluorobenzene-1-sulfonyl chloride.
The above synthesis methods have their own advantages and disadvantages. In practice, when considering the availability of raw materials, cost considerations, product purity requirements, and many other factors, the choice should be weighed.
What are the precautions for 3-Chloro-4-Fluorobenzene-1-Sulfonyl Chloride in storage and transportation?
3-Chloro-4-fluorobenzene-1-sulfonyl chloride requires more attention when storing and transporting.
First, storage should be in a cool, dry and well-ventilated place because of its corrosive and chemical activity. It must not be placed in a high temperature place to prevent its chemical properties from changing due to excessive temperature and causing danger. Furthermore, the storage place should be kept away from fires and heat sources, and avoid mixing with flammable, flammable and reducing agents. Because if it comes into contact with these substances, it may cause severe chemical reactions and cause disasters.
And it must be contained in a special container, which must be resistant to its corrosion and must be well sealed to prevent leakage. Every time you take it, you should also be careful. Seal it immediately after use to maintain the stability of its storage environment.
As for transportation, transportation personnel must be well versed in its characteristics and emergency response methods. Transportation equipment also needs to be strictly inspected to ensure that there is no risk of leakage. During transportation, you should drive steadily and slowly to avoid violent vibrations, collisions, and prevent container damage. If you pass through densely populated areas or important traffic areas, you need to be more careful. According to the specified route, you cannot change it at will.
If a leak unfortunately occurs, emergency response must be prompt. Evacuate the surrounding crowd, isolate the leakage area, and strictly prohibit unrelated people from approaching. Disposal personnel must wear professional protective equipment to avoid direct contact. Small leaks can be absorbed by inert materials such as sand and vermiculite; large leaks need to be built embankments or dug for containment, and then properly handled.
In short, in the storage and transportation of 3-chloro-4-fluorobenzene-1-sulfonyl chloride, all links must be carefully handled and strictly followed to ensure safety.
3-Chloro-4-Fluorobenzene-1-Sulfonyl impact of Chloride on the environment and human health
3-Chloro-4-fluorobenzene-1-sulfonyl chloride is a chemical commonly used in organic synthesis. Its impact on the environment and human health is of great concern to the world.
At the environmental end, if this chemical is released into nature, it may pollute water, soil and air. It may be difficult to degrade, and can be retained in the environment for a long time, and then accumulate. In aquatic ecosystems, it may cause poisoning to aquatic organisms, destroying their normal growth, reproduction and behavior. In the soil, it may affect the activity and community structure of soil microorganisms, thereby causing negative effects on soil fertility and plant growth. And it evaporates into the atmosphere, or participates in photochemical reactions, which have adverse effects on air quality.
As for human health, 3-chloro-4-fluorobenzene-1-sulfonyl chloride is irritating. If people come into contact with this substance, whether it is skin contact, inhalation of its volatile gas, or accidental ingestion, it can cause health problems. Skin contact may cause redness, swelling, pain, and burns; eye contact may damage eye tissue and affect vision. Inhalation of the volatile gas of this substance can irritate the respiratory tract, causing symptoms such as cough, asthma, and breathing difficulties. Long-term exposure may cause permanent damage to lung function. If ingested inadvertently, it may cause burns, nausea, vomiting, abdominal pain, etc., which is life-threatening in severe cases.
In summary, when using and handling 3-chloro-4-fluorobenzene-1-sulfonyl chloride, it is necessary to strictly follow safety operating procedures and take protective measures to reduce its harm to the environment and human health.