Chemical Formula | C8H6F2O |
Molecular Weight | 156.13 |
Appearance | Colorless to light yellow liquid |
Boiling Point | Data needed |
Melting Point | Data needed |
Density | Data needed |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents |
Vapor Pressure | Data needed |
Flash Point | Data needed |
Chemical Formula | C8H6F2O |
Molecular Weight | 156.13 |
Solubility In Water | Low solubility expected as it is an organic aromatic compound with fluorine and ether groups |
Stability | Stable under normal conditions, but may react with strong oxidizing agents |
Chemical Formula | C8H6F2O |
Molar Mass | 156.13 g/mol |
Appearance | Liquid (usually) |
Boiling Point | Data needed |
Melting Point | Data needed |
Density | Data needed |
Solubility In Water | Low solubility (expected, due to non - polar nature) |
Vapor Pressure | Data needed |
Flash Point | Data needed |
Refractive Index | Data needed |
What is the main use of 1-Petyloxy-2,3-difluorobenzene?
1-Phenoxy-2,3-difluorobenzene is one of the organic compounds. Its main use involves the field of organic synthesis.
In the field of organic synthesis, it is often used as a key intermediate. It can be converted into other organic compounds through various chemical reactions to meet different needs. For example, it can perform nucleophilic substitution reactions with other reagents to form new carbon-carbon bonds or carbon-heteroatom bonds, which is quite useful in creating complex organic molecular structures.
Or in the field of medicinal chemistry, it can be used as a basis for structural modification and modification, or new drugs with specific pharmacological activities can be developed. Due to the presence of fluorine atoms in molecules, the physical, chemical and biological properties of compounds can often be significantly changed, such as enhancing the lipid solubility of compounds, helping them to penetrate biofilms more easily, improving bioavailability; or affecting the interaction between compounds and biological targets, enhancing pharmacological activity and selectivity.
Furthermore, in the field of materials science, 1-phenoxy-2,3-difluorobenzene also has potential applications. It can be used as a raw material to participate in the preparation of special polymer materials, and its unique structure can endow materials with different properties, such as improving the thermal stability, chemical stability or optical properties of materials, to meet the needs of high-performance materials in electronic, optical and other industries. Overall, it is of great value in various fields such as organic synthesis, drug development, and material preparation, and has made significant contributions to promoting progress in related fields.
What are the physical properties of 1-Petyloxy-2,3-difluorobenzene?
1-Phenoxy-2,3-difluorobenzene is one of the organic compounds. Its physical properties are very important, and it is related to the application and characteristics of this substance.
First of all, its appearance is often colorless to light yellow transparent liquid, and it is clear when viewed, like a flow wave in a mirror, without the disturbance of variegated colors. Its smell has a special aromatic aroma. Although it is not as rich as a flower, it is also unique and can be recognized by smell.
The boiling point is within a specific temperature range, and this temperature is the key node for its transformation from liquid to gas. Just as the boiling point of water is 100 degrees Celsius, this compound also has its own boiling point. Under certain pressure conditions, when it reaches this temperature, it vaporizes and rises. The value of its boiling point is closely related to the interaction forces between molecules, such as van der Waals forces. This force maintains the aggregation of molecules. When the temperature rises, the molecules can break free and cause the state change of boiling point.
The melting point is the temperature at which a substance changes from a solid state to a liquid state. The melting point of 1-phenoxy-2,3-difluorobenzene is also a specific value. At this temperature, the molecules are arranged in a regular and orderly manner, and they are solid. As the temperature rises, the molecular motion intensifies, and the lattice structure loosens, it melts into a liquid state. < Br >
In terms of solubility, this compound exhibits good solubility in organic solvents and can be miscible with many organic solvents, such as alcohols, ethers, etc. This property is due to the similarity between its molecular structure and the molecules of organic solvents, following the principle of "similar phase dissolution". In water, its solubility is poor, because the polarity of water and the non-polar structure of the compound are quite different, the intermolecular forces between the two are difficult to match, so it is difficult to dissolve.
Density is also one of its important physical properties. At a specific temperature, its density is constant, which is an indicator to measure the relationship between its mass and volume. This value reflects the degree of close packing of molecules, which is of great significance for related process operations and product design.
The above physical properties are of great significance in the application of chemical engineering, materials and many other fields, and are related to the processing, storage and use of this compound.
Is 1-Petyloxy-2,3-difluorobenzene chemically stable?
The stability of the chemical properties of 1-phenoxy-2,3-difluorobenzene is related to many aspects.
In this compound, the phenoxy part and the benzene ring have a conjugated system, which is quite stable, the electron cloud is evenly distributed, and it is not easy to be easily invaded by general reagents. However, the oxygen atom is connected to the benzene ring, and its electronegativity difference makes the electron cloud density of the benzene ring change, or it shows activity under specific conditions.
In addition, the 2,3-difluoro substituent, the fluorine atom has extremely strong electronegativity, which produces an electron-absorbing effect on the benzene ring electron cloud, which decreases the electron cloud density of the benzene ring, resulting in the weakening of the electrophilic substitution reaction activity of the benzene ring, which increases the stability of the compound However, fluorine atoms can also enhance molecular polarity, or affect its solubility and interactions with other substances.
When it comes to chemical reactions, when encountering strong oxidants, although the benzene ring conjugation system is stable, the oxygen atom of the phenoxy group may be oxidized. In the nucleophilic substitution reaction, fluorine atoms can be partially positively charged with ortho-carbon due to their high electronegativity, or attract nucleophilic reagents to attack.
Under common conditions, if there are no extreme factors such as strong acid-base, strong oxidant or high temperature, the chemical properties of 1-phenoxy-2,3-difluorobenzene are still stable. However, in the complex system of organic synthesis, due to different reaction conditions and reagents, its stability will also change accordingly, which must be carefully considered.
What is the production process of 1-Petyloxy-2,3-difluorobenzene?
The production process of 1-phenoxy-2,3-difluorobenzene is a crucial skill in the field of chemical synthesis. To make this substance, a specific chemical path is often followed, and each step needs to be carefully controlled.
Bear the brunt and prepare suitable starting materials. Generally speaking, a compound containing a benzene ring with a modifiable check point is selected, supplemented by a fluorine-containing reagent to lay the foundation for the introduction of fluorine atoms. If a specific halogenated benzene derivative is used as the starting point, the halogen atom activity of this halogen is suitable, which is convenient for subsequent reactions.
Subsequently, a phenoxy group is introduced. This process is often achieved by nucleophilic substitution. Select a phenoxy source, such as phenol salts, and meet the halogenated benzene derivatives under suitable reaction conditions. The temperature and solvent of the reaction are all key elements. If the temperature is too high, it may cause side reactions to breed; if the temperature is too low, the reaction rate will be slow. Common solvents, such as polar aprotic solvents, can effectively promote the ionization process and improve the reaction efficiency.
As for the introduction of fluorine atoms, nucleophilic fluorination is mostly used. Select high-efficiency fluorination reagents, such as alkali metal fluorides. The reaction system needs to be operated in an anhydrous environment, and the presence of water may cause the fluorination reagent to fail. In this step, precise control of the reaction conditions, such as reaction time and the amount of fluorination reagent, directly affects the purity and yield of the product.
During the synthesis process, various monitoring methods are also required. For example, thin-layer chromatography (TLC) is used to track the reaction process in real time to determine whether the reaction is completed. When the reaction is completed, the product needs to be separated and purified. Commonly used methods, such as column chromatography and recrystallization, aim to obtain high-purity 1-phenoxy-2,3-difluorobenzene. Column chromatography uses the difference in the partition coefficient of different substances between the stationary phase and the mobile phase to achieve material separation; the recrystallization method makes the product crystallize and precipitate from the solution according to the change of solubility of the substance at different temperatures, so as to achieve the purpose of purification.
What is the price range of 1-Petyloxy-2,3-difluorobenzene in the market?
I don't know the price range of 1 - Petyloxy - 2,3 - difluorobenzene in the market. This is a rather specialized and specific chemical substance, and its price is often determined by many factors.
First, the difficulty of preparation is the key factor. If the preparation process is complicated, requires multiple reactions, and the reaction conditions of each step are strict, and the purity of the raw material is extremely high, the cost will be high, and the price will also rise.
Second, the amount of market demand has a great impact. If an industry has strong demand for this substance and limited supply, the price will rise according to the reason of supply and demand; conversely, if the demand is small, the price may stabilize or even decline.
Third, the scale of production cannot be ignored. In large-scale production, the unit production cost may be reduced due to the scale effect, thus making the price more competitive; in small-scale production, the cost is relatively high and the price will be higher.
Fourth, fluctuations in the price of raw materials will also be transmitted to the price of the substance. If the price of raw materials required for production fluctuates, the price of this substance is also difficult to stabilize.
Because I do not know the specific supply and demand of this substance in the chemical market, preparation details, etc., it is difficult to determine its price range. If you want to know the details, you can consult chemical product suppliers, consult professional chemical product price information platforms, or consult senior people in the chemical industry to obtain a more accurate price range.