Chemical Formula | C6H2ClF3O2S |
Appearance | Typically a colorless to pale yellow liquid |
Boiling Point | Data may vary, around a certain elevated temperature |
Melting Point | Specific value depending on purity and conditions |
Density | Certain value in g/cm³ |
Solubility | Soluble in some organic solvents |
Flash Point | Determined value related to flammability |
Vapor Pressure | Corresponding value under specific conditions |
Stability | Stable under normal conditions, but reactive with certain substances |
Chemical Formula | C6H2ClF3O2S |
Molar Mass | 246.59 g/mol |
Appearance | Typically a colorless to pale - yellow liquid |
Boiling Point | Data may vary, but generally in a certain high - temperature range due to its molecular structure |
Density | Characteristic value based on its mass - volume relationship |
Solubility | Soluble in certain organic solvents like dichloromethane, less soluble in water |
Reactivity | Highly reactive towards nucleophiles due to the presence of sulfonyl chloride group |
Odor | Pungent odor |
Stability | Unstable under certain conditions, especially in the presence of moisture which can lead to hydrolysis |
Chemical Formula | C6H2ClF3O2S |
Molecular Weight | 230.59 |
Appearance | Typically a colorless to light - yellow liquid |
Odor | Pungent, characteristic sulfonyl chloride odor |
Density | Data needed (g/cm³) |
Boiling Point | Data needed (°C) |
Melting Point | Data needed (°C) |
Solubility In Water | Reacts with water |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, chloroform |
Stability | Unstable in the presence of water and moisture, hydrolyzes |
Hazard Class | Corrosive, harmful if inhaled, in contact with skin or if swallowed |
What are the main uses of 2,4,6-trifluorobenzene-1-sulfonyl chloride?
2%2C4%2C6-%E4%B8%89%E6%B0%9F%E8%8B%AF-1-%E7%A3%BA%E9%85%B0%E6%B0%AF%E7%9A%84%E4%B8%BB%E8%A6%81%E7%94%A8%E9%80%94%E5%9C%A8%E5%8D%9A%E5%88%86%E7%94%9F%E6%B4%BB%E4%B8%8E%E5%8C%BB%E7%96%97%E7%95%85%E9%97%A8%E4%B8%8A%E3%80%82
In terms of performance, it is often used as a raw material to create a variety of compounds. Because of its certain chemical properties, it can generate multiple anti-steps for the synthesis of compounds, helping to synthesize compounds with different diseases. In the field of research, some external ointments and water applications, this substance is added because it may play a role in solving diseases and promoting synthesis.
For daily use, 2%2C4%2C6-%E4%B8%89%E6%B0%9F%E8%8B%AF-1-%E7%A3%BA%E9%85%B0%E6%B0%AF is also useful in some high-end cleaning products. It can be used as a special addition, because it can be combined with other ingredients to increase the decontamination ability of cleaning products, or it can play a certain role in the treatment of products. The performance of the product makes the product more effective and stable in use.
In addition, it also plays an important role in some special chemical processes. For example, in specific synthetic antibodies, this compound can be used as a catalyst or a catalyst to accelerate the reaction, improve the reaction efficiency, and promote the chemical process to be completed more effectively, so as to produce chemical products that meet the needs. Moreover, 2%2C4%2C6-%E4%B8%89%E6%B0%9F%E8%8B%AF-1-%E7%A3%BA%E9%85%B0%E6%B0%AF have shown important uses in many fields by virtue of its characteristics.
What are the physical properties of 2,4,6-trifluorobenzene-1-sulfonyl chloride?
2%2C4%2C6-%E4%B8%89%E6%B0%9F%E8%8B%AF-1-%E7%A3%BA%E9%85%B0%E6%B0%AF, that is, 2,4,6-trifluoro-1-chlorobenzene. The physical properties of this substance are as follows:
It is a colorless to light yellow transparent liquid at room temperature and pressure, and it looks clear. Smell it, it has a special aromatic smell, which is more volatile and can spread rapidly in the air.
The boiling point is about 100-102 ° C. At this temperature, the liquid will transform into a gaseous state. Its melting point is about -45 ° C. When the temperature drops below the melting point, the substance will solidify from a liquid state to a solid state.
In terms of density, it is about 1.38 g/cm ³. Compared with the density of water, it is 1 g/cm ³. If mixed with water, it will sink to the bottom of the water.
This substance is slightly soluble in water. Due to the characteristics of its molecular structure, the interaction force with water molecules is weak, making it difficult to disperse uniformly in water. However, it can be well miscible with most organic solvents, such as ethanol, ether, acetone, etc., and can form a uniform solution with these organic solvents.
The vapor pressure of 2,4,6-trifluoro-1-chlorobenzene has a certain value at room temperature, which makes it volatile to a certain extent. The relative density of vapor is heavier than that of air. In places with poor ventilation, vapor is easy to accumulate at low places. Its refractive index also has a specific value. When light passes through the substance, it will be refracted at a specific angle. These physical properties are of great significance in applications in chemical engineering, pharmaceutical synthesis, and many other fields, and also guide the selection of their storage, transportation, and use methods.
What are the chemical properties of 2,4,6-trifluorobenzene-1-sulfonyl chloride?
2%2C4%2C6-%E4%B8%89%E6%B0%9F%E8%8B%AF-1-%E7%A3%BA%E9%85%B0%E6%B0%AF%E7%9A%84%E5%8C%96%E5%AD%A6%E6%80%A7%E8%B4%A8%E6%9C%89%E5%A6%82%E4%B8%8B%E4%B8%80%E4%BA%9B:
This is an organic compound with specific chemical properties. It can exhibit many reaction characteristics under specific conditions. For example, because of the specific functional groups contained in its structure, it can react with specific reagents. 2%2C4%2C6-%E4%B8%89%E6%B0%9F%E8%8B%AF-1-%E7%A3%BA%E9%85%B0%E6%B0%AF, certain atoms or groups contained can participate in nucleophilic substitution reactions. In case of nucleophilic reagents, some of its atoms or groups may be replaced by nucleophilic reagents, resulting in the formation of new compounds.
Furthermore, this compound may undergo oxidation reactions under specific conditions. Specific parts of the molecular structure can be oxidized under the action of appropriate oxidants, causing changes in its chemical structure and properties. This oxidation reaction may also affect its physical properties, such as color, solubility, etc.
In addition, 2%2C4%2C6-%E4%B8%89%E6%B0%9F%E8%8B%AF-1-%E7%A3%BA%E9%85%B0%E6%B0%AF can also participate in addition reactions. When encountering reagents with unsaturated bonds, an addition reaction can occur, allowing the molecular structure to expand and change, and generating new chemical substances. This addition reaction may be used to prepare organic compounds with specific structures and functions, which is of great significance in the field of organic synthesis.
In terms of solubility, due to the polarity and structural characteristics of molecules, the solubility varies in different solvents. It may have good solubility in some organic solvents, but poor solubility in water. This solubility characteristic needs to be considered when separating, purifying and reacting them. In short, the chemical properties of 2%2C4%2C6-%E4%B8%89%E6%B0%9F%E8%8B%AF-1-%E7%A3%BA%E9%85%B0%E6%B0%AF are rich and diverse, and have extensive research and application value in the field of organic chemistry.
What is the preparation method of 2,4,6-trifluorobenzene-1-sulfonyl chloride?
To prepare 2,4,6-tribromo-1-nitrobenzene, the method is as follows:
First take benzene as the starting material, mix concentrated sulfuric acid with concentrated nitric acid to obtain a mixed acid. The benzene is gradually added to the mixed acid, and the temperature is appropriately controlled to nitrate it to obtain nitrobenzene. In this step, pay attention to the control of temperature, so as not to cause side reactions to occur.
Then, take out the nitrobenzene, mix it with liquid bromine, and use iron powder or iron tribromide as the catalyst. Under appropriate conditions, the two start a substitution reaction. The nitro group is the meta-locator group, and the bromine atom is then mainly inserted into the position between the nitro groups to obtain 2,4,6-tribromo-1-nitrobenzene.
During the reaction, the device needs to be sealed to prevent the escape of bromine and other harmful gases, and attention should be paid to the amount of catalyst, too much or too little can affect the process and yield of the reaction. In addition, after the reaction is completed, the product needs to be separated and purified, such as extraction, distillation, recrystallization, etc., to obtain pure 2,4,6-tribromo-1-nitrobenzene. In this way, the method of preparing this compound can be obtained.
What are the precautions for using 2,4,6-trifluorobenzene-1-sulfonyl chloride?
2% 2C4% 2C6-tribromo-1-octenonitrile is a dangerous chemical. During use, the following things must be paid attention to:
First, protective measures must be taken. Because of its toxicity and irritation, when coming into contact, wear appropriate protective equipment. Such as wearing protective gloves to prevent skin contact with it, corrosion or absorption and damage; wearing protective glasses to prevent it from splashing into the eyes and causing serious damage to the eyes; at the same time, wearing a gas mask to prevent inhalation of its volatile gases and damage to the respiratory tract.
Second, storage conditions must be strictly controlled. Store in a cool, well-ventilated place, away from fire and heat sources. Because it is a flammable substance, in case of open flames and hot topics, it is easy to cause combustion and explosion, endangering life and property safety. And it should be stored separately from oxidants, acids, alkalis, etc., and should not be mixed to prevent chemical reactions from occurring and leading to dangerous conditions.
Third, the operation process should be careful and meticulous. When using, it should be carried out in a fume hood to ensure air circulation and timely discharge of volatile harmful gases. During operation, avoid contact with skin, eyes and respiratory tract. In case of accidental contact, appropriate first aid measures should be taken immediately. If skin contact, immediately rinse with a large amount of flowing water, and then seek medical treatment; eye contact, should immediately lift the eyelids, rinse thoroughly with a large amount of flowing water or normal saline, and seek medical attention quickly; if inhalation, should quickly leave the scene to fresh air, keep the respiratory tract unobstructed, such as breathing difficulties, give oxygen, such as breathing stops, immediately perform artificial respiration, and seek medical attention.
Fourth, the emergency treatment plan should be complete. The workplace needs to be equipped with suitable leakage emergency treatment equipment and materials. In the event of a leak, the personnel in the leakage contaminated area should be quickly evacuated to a safe area, and quarantined, and access should be strictly restricted. To cut off the source of fire, it is recommended that emergency personnel wear self-contained positive pressure breathing apparatus and anti-toxic clothing. Cut off the source of leakage as much as possible to prevent it from flowing into restricted spaces such as sewers and drainage ditches. In the event of a small leak, it can be absorbed by sand, vermiculite or other inert materials; in the event of a large leak, build a dike or dig a pit to contain it, cover it with foam to reduce vapor disasters, and transfer it to a tanker or dedicated collector for recycling or transportation to a waste treatment site for disposal.