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What are the main uses of O-Cyanotrifluoromethoxybenzene?
O-cyanotrifluoromethoxylbenzene is also an organic compound. Its main uses cover a wide range of fields.
In the field of pharmaceutical chemistry, this compound is often a key intermediate. Pharmaceutical synthesis requires delicate construction of molecular structures. O-cyanotrifluoromethoxylbenzene, with its special chemical properties, can introduce unique groups to help create novel active drug molecules. For example, when developing specific anti-cancer drugs, it can participate in key reaction steps to make drug molecules more suitable for cancer cell targets, enhance curative effect, and reduce damage to normal cells.
In the field of materials science, it also has its uses. Because it contains functional groups such as fluorine and cyano, it can give materials special properties. When preparing high-performance polymer materials, the introduction of this compound can improve the thermal stability, chemical stability and electrical properties of the material. Taking the insulating material used in electronic devices as an example, after adding this compound, the material can work stably in harsh environments such as high temperature and high humidity, improving the reliability and service life of electronic devices.
Furthermore, in the field of pesticide chemistry, O-cyanotrifluoromethoxybenzene also plays an important role. The creation of pesticides requires efficient and environmentally friendly ingredients. This compound can add unique activity to pesticide molecules, enhance the inhibition and killing ability of pests and bacteria, and reduce the residue in the environment, which is in line with the needs of modern green pesticide development. In conclusion, O-cyanotrifluoromethoxy benzene, with its unique chemical structure, is an indispensable and important substance in many fields such as medicine, materials, and pesticides, promoting technological progress and innovation in various fields.
What are the physical properties of O-Cyanotrifluoromethoxybenzene?
O-cyanotrifluoromethoxylbenzene is an important member of the field of organic compounds. Its physical properties are quite characteristic. Under normal temperature and pressure, it usually appears as a colorless to light yellow liquid form. This appearance characteristic makes it unique among many compounds.
Looking at its odor, it often emits a weak and irritating odor. Although this odor is not strong, it is enough to attract attention and add a unique label to its properties.
When it comes to solubility, this compound shows a specific tendency. It has good solubility in organic solvents, such as common toluene and dichloromethane, and can fuse with these solvents to form a uniform system. However, the solubility in water is extremely limited, and it is difficult to miscible with water. This property is closely related to the chemical properties contained in its molecular structure.
In terms of boiling point, its value is in a certain range, roughly around [X] ° C (the specific value varies depending on the measurement conditions). The existence of boiling point determines the temperature node at which the phase transition occurs during the heating process of the compound, and has a profound impact on its application in chemical production, experimental operation and other fields.
In terms of melting point, it is about [X] ° C (also subject to the measurement conditions). The characteristics of melting point are related to the conversion conditions between solid and liquid states, providing a key reference for related process design and practical application. The density of
is also one of its important physical properties, which is about [X] g/cm ³. This density value reflects the mass of the compound per unit volume and plays an indispensable role in operations such as substance measurement and mixing ratio. The many physical properties of
O-cyanotrifluoromethoxylbenzene work together to build its unique physical "portrait" and lay a solid foundation for people to study and apply it in different fields. Whether it is in the exploration of organic synthesis chemistry experiments or the planning of chemical production processes, these physical properties are key factors to consider, enabling people to precisely control and use this compound.
Is O-Cyanotrifluoromethoxybenzene chemically stable?
The stability of the chemical properties of O-cyanotrifluoromethoxy benzene depends on many factors. This compound contains two functional groups of cyanide (CN) and trifluoromethoxy (-OCF). The cyanyl group has high reactivity. Because the carbon-nitrogen triple bond is rich in electrons, it can participate in many reactions, such as nucleophilic addition and hydrolysis. When hydrolyzed, the cyanyl group can be converted into a carboxyl group, which shows that it is active.
And the trifluoromethoxy group, due to the extremely high electronegativity of the fluorine atom, has a strong electron-absorbing effect, which can reduce the electron cloud density of the benzene ring, and reduce the activity of the benzene ring in the electrophilic substitution reaction.
However, from another perspective, in the molecular structure of O-cyanotrifluoromethoxy benzene, the conjugated system of the benzene ring has a certain stabilizing effect on the functional group. The conjugated system of the benzene ring can disperse electrons and reduce the overall energy of the molecule. Although the cyano group and the trifluoromethoxy group have their own characteristics of activity, they are bound to each other due to the conjugation of the benzene ring. Under specific conditions, the compound has certain stability.
If the environmental conditions are suitable, such as low temperature and no active reagents, O-cyanotrifluoromethoxy benzene can maintain a relatively stable state. However, under conditions such as high temperature, strong acid, strong base or strong oxidant, the cyano group and the trifluoromethoxy group may react, and the stability will be destroyed.
In summary, the chemical stability of O-cyanotrifluoromethoxylbenzene cannot be generalized, depending on the specific external conditions and the substances in contact with it.
What are O-Cyanotrifluoromethoxybenzene synthesis methods?
There are various methods for the synthesis of O-cyanotrifluoromethoxylbenzene. One method can also start from o-hydroxybenzonitrile. Mix o-hydroxybenzonitrile with trifluoromethoxylation reagent, and under suitable reaction conditions, make the two chemically react. The trifluoromethoxylation reagent is either a combination of trifluoromethyl halide and base, or other compounds with active trifluoromethoxy. When reacting, it is necessary to pay attention to the reaction temperature, reaction time and the ratio of reactants, which are all related to the effectiveness of the reaction. If the temperature is too high, it may cause more side reactions; if the temperature is too low, the reaction rate will be slow. Proper regulation of these factors can make the reaction proceed smoothly in the direction of generating O-cyanotrifluoromethoxylbenzene.
Another method is to prepare an intermediate containing trifluoromethoxy group first, and then react it with a cyanogen-containing reagent. For example, with suitable raw materials, a series of reactions can be carried out to obtain an aromatic hydrocarbon derivative containing trifluoromethoxy. Later, the cyanide group is introduced into this derivative by cyanation reaction to obtain O-cyanotrifluoromethoxylbenzene. This approach also requires careful control of the conditions of each step of the reaction to achieve the ideal yield and purity. The cyanide reagent used may be potassium cyanide, sodium cyanide and other common cyanides. In the reaction system, the reaction with the intermediate needs to be carried out in the presence of suitable solvents and catalysts.
In addition, other functionalized benzene derivatives are also used as starting materials, and O-cyanotrifluoromethoxybenzene is finally obtained by gradual conversion of functional groups. Each method has its own advantages and disadvantages. In actual synthesis, it is necessary to weigh and choose according to the availability of raw materials, the difficulty of reaction, cost and many other factors. In this way, O-cyanotrifluoromethoxybenzene can be synthesized efficiently and economically.
What is the price range of O-Cyanotrifluoromethoxybenzene in the market?
I have not obtained the exact number of O-Cyanotrifluoromethoxybenzene in the market price range. The price of this compound may vary greatly due to changes in use, purity, supply and demand.
If you want the price, you can go to the chemical product trading platform and reagent supplier for details. On the chemical product trading platform, such as Gade Chemical Network, etc., many chemical product price information is common, but the price may vary from time to time, and it is also subject to negotiation between the two parties. Reagent suppliers, such as Sinopharm Group Chemical Reagent Co., Ltd., search banner reagent, etc., are often priced according to product specifications and purity. The price of high purity must be higher than that of ordinary purity.
Or due to market supply and demand, if the demand for this product is strong and the supply is small, the price will rise; conversely, if the supply is large and the demand is small, the price will fall.
To know the market price of O-Cyanotrifluoromethoxybenzene, go to the relevant platform or consult the supplier in person to get an accurate price.
