Chemical Formula | C12F10S |
Molar Mass | 366.18 g/mol |
Appearance | Solid (presumably, based on common nature of such organofluorine compounds) |
Physical State At Room Temp | Solid |
Solubility In Water | Very low, as it is a non - polar fluorinated aromatic compound |
Solubility In Organic Solvents | Soluble in non - polar organic solvents like toluene, hexane etc. |
Stability | Stable under normal conditions, but can react under extreme conditions with strong oxidizing or reducing agents |
Toxicity | Toxicity data may be limited, but fluorinated aromatic compounds can have potential toxicity |
Chemical Formula | C12F10S |
Molecular Weight | 346.18 |
Appearance | Typically a solid (physical state may vary based on conditions) |
Solubility | Limited solubility in water, likely soluble in some organic solvents |
Density | No general - known value without specific data source |
Vapor Pressure | Low vapor pressure expected due to structure |
Stability | Stable under normal conditions, but reacts with strong oxidizing agents |
Chemical Formula | C12F10S |
Molecular Weight | 354.18 |
Appearance | Typically a solid (physical state may vary based on conditions) |
Solubility In Water | Expected to be low, non - polar compound |
Solubility In Organic Solvents | May be soluble in non - polar organic solvents like toluene |
Vapor Pressure | Low vapor pressure due to high molecular weight and non - volatile nature |
Stability | Stable under normal conditions, may be reactive under extreme conditions |
What is the main use of 1,1 '-sulfanediylbis (pentafluorobenzene)?
1% 2C1% 27 '-sulfanediylbis (pentafluorobenzene), often referred to as 1,1' -thiobis (pentafluorobenzene), is widely used.
In the field of chemical synthesis, it is often used as a special intermediate. It can be ingeniously integrated into complex organic molecular structures through specific chemical reactions, paving the way for the creation of new materials with unique properties. For example, in the preparation of high-end fluoropolymers, 1,1 '-thiobis (pentafluorobenzene) can be used as a key monomer to participate in the polymerization reaction, giving the polymer excellent chemical stability, weather resistance, and low surface energy. Such polymers are widely used in high-end fields such as aerospace and electronic devices. < Br >
In the field of materials science, due to the particularity of fluorine-containing structure, the surface properties of materials can be significantly improved. Adding it to coating materials can improve the waterproof, oil-proof and anti-fouling properties of coatings, making the surface of coated objects smoother and easier to clean. It has potential applications in building materials, automotive coatings, etc.
In organic synthesis chemistry, it is an important starting material for the construction of complex compounds containing sulfur and fluorine. Chemists can design and synthesize a series of organic compounds with novel structures and specific functions through the selective reaction of sulfur atoms and fluorine atoms on the benzene ring, which is also of great significance for the exploration of new drug molecular structures in the field of medicinal chemistry, providing more possible structural templates for the development of specific new drugs. In conclusion, 1,1 '-thiobis (pentafluorobenzene) plays an indispensable role in many scientific and industrial fields due to its unique molecular structure.
What are the physical properties of 1,1 '-sulfanediylbis (pentafluorobenzene)?
1% 2C1% 27 -sulfanediylbis (pentafluorobenzene), this is an organic compound, Chinese name 1,1 '-thiobis (pentafluorobenzene). The physical properties of this substance are very important and are of significance for chemical research and related industrial applications.
Its properties are usually solid, and it may be white to white-like powder. This color state is conducive to preliminary identification. As far as the melting point is concerned, it has been experimentally determined to be about a certain temperature range. This melting point characteristic has an important impact on its phase change under specific conditions, and is related to its stability under different temperature environments.
Solubility is also a key physical property. In common organic solvents, such as certain aromatic hydrocarbons and halogenated hydrocarbon solvents, 1,1 '-thiobis (pentafluorobenzene) exhibits a certain solubility. Moderate dissolution in such solvents provides the possibility for them to participate in many organic reactions, because they can fully contact and collide with other reactants in the solution environment, and then promote the reaction process.
In addition, the density of this substance is also a characteristic. Although the specific value needs to be accurately measured, the density is crucial when it involves operations such as mixing and separation of substances, and is related to its distribution and behavior in the system.
Furthermore, the volatility of 1,1 '-thiobis (pentafluorobenzene) is relatively low, which makes it not easy to be lost due to volatilization under normal temperature and pressure, which is conducive to storage and transportation. In practical application scenarios, it can reduce the loss and potential danger caused by volatilization.
In summary, the white powder appearance, specific melting point, solubility, density and low volatility of 1,1' -thiobis (pentafluorobenzene) together determine its application scope and mode in the chemical field. It has unique value in many aspects such as organic synthesis and material preparation.
What are the chemical properties of 1,1 '-sulfanediylbis (pentafluorobenzene)
1% 2C1% 27 - sulfanediylbis (pentafluorobenzene), this is an organic compound with interesting chemical properties. Under the paradigm of "Tiangong Kaiji", and in ancient Chinese, it is the way of the king.
This compound has certain stability. In its molecular structure, the benzene ring is connected to the sulfur atom. Due to the conjugated system of the benzene ring, it has a certain degree of chemical inertness and is difficult to participate in general simple chemical reactions. However, when encountering a strong oxidant, its sulfur atom may be oxidized, causing the structure and properties of the compound to change.
In terms of solubility, due to its large number of fluorine atoms, it has a certain lipophilicity. It should have good solubility in organic solvents such as dichloromethane and chloroform, but poor solubility in water. This is because the polarity of water is contrary to the non-polar structure of the compound.
On its reactivity, although the fluorine atom on the benzene ring has an electron-absorbing effect, which reduces the electron cloud density of the benzene ring, under certain conditions, if it encounters a nucleophilic reagent, the fluorine atom can be replaced, resulting in the formation of new compounds. And the sulfur atom can be used as a nucleophilic check point to participate in the nucleophilic substitution reaction, and react with halogenated hydrocarbons and other reagents to derive compounds with different structures. < Br >
And because of its fluoride content, the compound may have certain thermal and chemical stability, and in high temperatures or special chemical environments, it is more able to maintain its own structural integrity than ordinary organic compounds. This property may make it potentially useful in the fields of special material synthesis and fine chemistry.
What is the synthesis method of 1,1 '-sulfanediylbis (pentafluorobenzene)
1% 2C1% 27 - sulfanediylbis (pentafluorobenzene) is 1,1 '-thiobis (pentafluorobenzene), which is synthesized as follows:
To prepare 1,1' -thiobis (pentafluorobenzene), pentafluorobenzene and sulfur-containing reagents are often used as starting materials. In the past, pentafluorobenzene and sodium sulfide were used as reactants. First take an appropriate amount of pentafluorobenzene, place it in a dry reactor, dissolve it in an organic solvent such as N, N - dimethylformamide (DMF), and disperse it uniformly. Then, slowly drop the aqueous solution of sodium sulfide into the reactor, stir it at the same time, and strictly control the reaction temperature within an appropriate range, generally about 60 - 80 degrees Celsius. In this process, the bromine atom of pentafluorobromobenzene undergoes a nucleophilic substitution reaction with the sulfur ion of sodium sulfide, and the sulfur atom gradually connects two pentafluorobenzene groups to form 1,1 '-thiobis (pentafluorobenzene).
After the reaction is completed, the reaction mixture is treated by conventional separation and purification methods. First, it is diluted with water, then the product is extracted with an organic solvent such as dichloromethane, the organic phases are combined, and dried with anhydrous sodium sulfate to remove the moisture. Subsequently, the organic solvent is removed by vacuum distillation, and the fraction with a specific boiling point range is collected. This fraction is the purified 1,1' -thiobis (pentafluorobenzene).
There are also those who use pentafluoroiodobenzene as raw material, this reaction activity is higher, and the reaction conditions may be slightly slower. However, the cost of pentafluoroiodobenzene is higher, and the advantages and disadvantages need to be weighed in practical application. This synthesis method focuses on the purity of raw materials, the precise control of reaction conditions, and the fine operation of separation and purification to obtain high-purity 1,1 '-thiobis (pentafluorobenzene).
What are the precautions for 1,1 '-sulfanediylbis (pentafluorobenzene) during storage and transportation?
1% 2C1% 27 -thiane diyl bis (pentafluorobenzene) is a special chemical substance. There are many things to pay attention to during storage and transportation.
The first thing to pay attention to is its chemical properties. This substance has specific chemical activity, and may react violently when encountering certain substances. Therefore, when storing, it must be kept away from active metals, strong oxidizing agents, etc. If mixed with it, it may cause unpredictable chemical reactions, which may cause safety concerns. And it may also be sensitive to moisture, moisture intrusion, or deterioration, which will damage its chemical properties. It must be stored in a dry and airtight place.
times and temperature and light. If the temperature is too high, it may cause the substance to decompose and evaporate. Therefore, it should be stored in a cool place, away from direct sunlight. Strong light exposure, or luminescent chemical reactions, change its structure and properties.
In addition, the choice of packaging is also crucial. Transportation and storage, both need to be packed in a suitable package. The packaging should have good sealing to prevent leakage. And the material must be resistant to the corrosion of the substance and not react with it.
During transportation, shock resistance is also key. Violent vibration or damage to the package, causing material leakage. Driving should be smooth and avoid bumps.
In summary, the storage and transportation of 1% 2C1% 27-thiane diyl bis (pentafluorobenzene) requires careful inspection of its chemical properties, attention to temperature, humidity, light, appropriate packaging, and shock absorption during transportation, so as to ensure its safety and not damage its properties.