O-Nitrotrifluoromethoxybenzene, or o-nitrotrifluoromethoxylbenzene, has a wide range of uses. In the field of organic synthesis, it is often used as a key intermediate. Due to its rich trifluoromethoxy and nitro groups in the molecule, this difunctional group has unique activities and can participate in multiple chemical reactions and help synthesize other fluorinated organic compounds.
In terms of medicinal chemistry, the addition of trifluoromethoxy to organic molecules can significantly change their physicochemical properties, biological activities and metabolic characteristics. With o-nitrotrifluoromethoxylbenzene, chemists can create lead compounds with unique pharmacological activities, which are expected to develop new specific drugs. For example, in the development of some anticancer and antiviral drugs, trifluoromethoxy-containing structural units can enhance the binding force between the drug and the target and improve the efficacy.
In the field of materials science, o-nitrotrifluoromethoxylbenzene is also useful. After a specific chemical reaction, it can be introduced into polymer materials, giving the material excellent characteristics such as weather resistance, chemical stability, and low surface energy. For example, when applied to coatings, plastics, and other materials, it can improve the material's corrosion resistance and wear resistance, and broaden the scope of application of the material.
In addition, in pesticide chemistry, it can be used as an intermediate to synthesize highly efficient, low-toxic, and environmentally friendly pesticides. The presence of trifluoromethoxy can enhance the effect of pesticides on pest targets, reduce the dosage, and reduce the negative impact on the environment.

O-Nitrotrifluoromethoxybenzene, Chinese name o-nitrotrifluoromethoxylbenzene. Its physical properties are as follows:
This substance is mostly liquid at room temperature, and it is clear and has a specific flow texture. Its color is often nearly colorless to slightly yellow. When placed under light, it can be seen that the light penetrates slightly yellowing. Smell it, there is a pungent smell, this smell is distinct and penetrating, and its chemical properties can be quickly sensed.
Its boiling point is in a specific range, usually around [X] ° C. The boiling point temperature is the critical temperature for a substance to change from liquid to gas. At this temperature, molecules gain enough energy to overcome intermolecular forces and escape from the liquid surface. The melting point is about [X] ℃. When the temperature drops below the melting point, the molecular movement slows down, and they are close to each other and arranged in an orderly manner, so they solidify from liquid to solid.
In terms of density, it is different from water, with a value of about [X] g/cm ³. Due to the characteristics of molecular structure and constituent atoms, its mass is different from that of water at the same volume. Solubility is also an important physical property. In organic solvents such as ethanol and ether, it shows good solubility and can be miscible with these solvents in a certain proportion. However, in water, the solubility is very small, because the molecular polarity of this substance is quite different from that of water molecules, and it follows the principle of "similar miscibility". The refractive index of
has a specific value, which is about [X]. This property is related to the refractive ability of molecules to light, reflecting the influence of the internal structure of a substance on the direction of light propagation. By measuring the refractive index, the purity and characteristics of the substance can be identified.

O-nitrotrifluoromethoxylbenzene is also an organic compound. Its chemical properties are open to investigation.
In terms of reactivity, due to the presence of nitro and trifluoromethoxy groups on the benzene ring, and the nitro group is a strong electron-absorbing group, the electron cloud density of the benzene ring is reduced, and the electrophilic substitution reactivity of the benzene ring is reduced. Moreover, the electron cloud density of the neighboring and para-position of the nitro group is particularly reduced, so the electrophilic reagents attack the intermediate position more. Although the trifluoromethoxy group is also an electron-absorbing group, its effect on the electron cloud density of the benzene ring is intertwined with the nitro group, which makes the reactivity more unique.
In terms of stability, the presence of nitro groups increases the molecular energy and reduces the stability. And the nitro group is prone to reactions such as reduction under specific conditions, which affects the overall structure of the molecule. The trifluoromethoxy gene contains fluorine atoms and has strong electronegativity, which can enhance the stability of the molecule. However, due to the influence of nitro groups, its stability is not very high.
In terms of solubility, because it is an organic compound, and the molecular polarity is changed by nitro and trifluoromethoxy, it has a certain solubility in organic solvents such as dichloromethane and chloroform, but it has little solubility in water, and its hydrophobic organic structure dominates.
In terms of thermal stability, when heated, nitro groups may decompose and other reactions, resulting in molecular structure changes and poor thermal stability. However, trifluoromethoxy has a certain tolerance to heat, which also affects its thermal stability to a certain extent. Its chemical properties are formed by the interaction of various groups in its structure. In organic synthesis and other fields, because of its unique chemical properties, it can be used as a key intermediate to participate in various chemical reactions to produce various organic compounds.

O-nitrotrifluoromethoxylbenzene is an important compound in organic synthesis. There are various methods for its preparation.
First, trifluoromethoxylbenzene can be started. First, trifluoromethoxylbenzene is nitrified with an appropriate nitrifying agent, such as a mixed acid of nitric acid and sulfuric acid, under suitable reaction conditions. In this process, the reaction temperature, the proportion of reactants and the reaction time need to be carefully adjusted. If the temperature is too high, it may cause side reactions such as polynitrification, resulting in unnecessary products; if the temperature is too low, the reaction rate will be slow and the yield will not be good. In general, the reaction temperature should be controlled in a moderate range. The function of sulfuric acid is, firstly, a water absorber to maintain the acidic environment of the reaction system, and secondly, it can promote the formation of nitric acid to nitroyl positive ions (NO ²), which is an active intermediate for nitrification reaction.
Second, it can also be obtained by introducing trifluoromethoxy through the step of introducing trifluoromethoxy from benzene derivatives containing appropriate substituents. When introducing trifluoromethoxy, you can choose to use trifluoromethoxy reagents such as some halides or other active compounds containing trifluoromethoxy groups. In the presence of bases and catalysts, nucleophilic substitution reactions occur with benzene derivatives to introduce trifluoromethoxy groups. Then, according to the conventional nitrification method, nitro groups are introduced into the benzene ring to obtain O-nitrotrifluoromethoxylbenzene. However, in this path, the reaction conditions of each step also need to be precisely controlled to ensure the selectivity and yield of the reaction.
Preparation of O-nitrotrifluoromethoxylbenzene, no matter what method, it is necessary to pay attention to the precise control of the reaction conditions, and the post-treatment process is also very important. Steps such as extraction, distillation, and recrystallization are often required to purify the product to obtain high-purity O-nitrotrifluoromethoxylbenzene.

In my opinion, this "O-Nitrotrifluoromethoxybenzene" is an organic compound. It is difficult to say exactly what it is in the market price range. Because of the market price, it is often affected by many factors.
First, the difficulty of obtaining raw materials. If the raw materials required for the preparation of this compound are widely sourced and easily available, the cost may be slightly lower, and the price will stabilize accordingly. However, if raw materials are scarce, difficult to collect, or complex refining methods are required, the price will rise due to rising costs.
Second, the complexity of the preparation process. If the preparation process is simple, the equipment requirements are normal, the energy consumption is low, and the production efficiency is high, the price may be close to the people. On the contrary, if the process is complicated, special equipment and superb technology are required, and the production process has many twists and turns, it is time-consuming and labor-intensive, and the price is not cheap.
Third, the situation of market supply and demand. If the market demand for this product is strong, but the supply is limited, the demand exceeds the supply, and the price will rise. If there is little demand and excess supply, the price may be lowered in order to make a sale.
Fourth, the manufacturers are different. The prices set by each manufacturer vary depending on the technical level, management efficiency, and operating costs. Well-known large factories have excellent quality and high prices; small factories compete for the market or use low prices as a strategy.
To sum up, in order to know the exact price range of "O-Nitrotrifluoromethoxybenzene", it is necessary to carefully investigate many conditions such as raw materials, processes, supply and demand, and manufacturers to obtain a more accurate number. However, at present, it is difficult to determine the range of its market price based on this name alone.