3 - (difluoromethoxy) iodobenzene, this substance has a wide range of uses. In the field of organic synthesis, its position is pivotal. Due to its unique structure, difluoromethoxy coexists with iodine atoms, and can be used as a key intermediate to participate in the preparation of many complex organic compounds.
First, in pharmaceutical chemistry, with its special structure, it can be used to construct molecular frameworks with specific biological activities. By reacting with other reagents, the molecular structure can be precisely modified, which in turn affects the interaction between drugs and targets, and improves the efficacy and selectivity of drugs. For example, in the development of some new anti-cancer drugs or antiviral drugs, 3- (difluoromethoxy) iodobenzene may serve as a starting material or a key intermediate to help create more effective therapeutic drugs.
Second, in the field of materials science, it also has outstanding performance. Because its structure endows compounds with specific electrical and optical properties, it can be used to synthesize organic optoelectronic materials. For example, when preparing organic Light Emitting Diode (OLED) materials, the introduction of 3- (difluoromethoxy) iodobenzene structural units may optimize the luminous efficiency and stability of the materials, contributing to the improvement of display technology performance.
Furthermore, in pesticide chemistry, this compound can be used as an important raw material for the synthesis of new pesticides. After proper chemical transformation, the synthesized derivatives may have highly effective insecticidal and bactericidal activities, and are environmentally friendly, contributing to the development of green and sustainable agricultural production.

3 - (difluoromethoxy) iodobenzene is also an organic compound. It has unique physical properties and has attracted much attention in the fields of chemical industry and scientific research.
Under normal temperature, it is mostly colorless to light yellow transparent liquid. This state makes it easy to disperse and mix in many reaction systems, providing convenience for the smooth development of chemical reactions. Its odor may have a special aromatic smell, but the strength of this smell often varies depending on the environment and concentration.
When it comes to boiling point, it is in a specific temperature range due to the force between molecules. This temperature can change it from liquid to gaseous. The characteristics of this boiling point are of great significance in the operation of separation and purification. It can be effectively separated from the mixture by distillation according to the difference in boiling point.
As for the melting point, it is also an important physical property. Under a specific temperature, it will melt from solid to liquid. The accurate determination of this temperature helps to identify the purity of the substance. The higher the purity, the narrower the melting point range.
In terms of solubility, 3- (difluoromethoxy) iodobenzene exhibits good solubility in organic solvents, such as common ethanol, ether, dichloromethane, etc., and can be miscible with various solvents. This property makes it widely used in organic synthesis reactions, participating as a reactant or solvent. In water, its solubility is poor, due to the dominant role of hydrophobic groups in the molecular structure.
Density is one of the important markers of substances. The density of 3- (difluoromethoxy) iodobenzene may be different from that of water. This difference can be used as an important basis for judgment in operations such as liquid-liquid separation.
In addition, its vapor pressure has a specific value at a certain temperature, and the vapor pressure is related to the degree of volatilization of the substance. This property is of great significance for safety precautions and the formulation of operating norms during storage and use. The above physical properties are interrelated and together determine the behavior and use of 3- (difluoromethoxy) iodobenzene in different scenarios.

There are various ways to prepare 3 - (difluoromethoxy) iodobenzene. One is to use methoxy-containing benzene as the starting material, first through halogenation reaction, introduce iodine atoms at specific positions in the benzene ring. In this case, the halogenation reagents and reaction conditions need to be carefully selected to ensure that the iodine atoms are accurately added to the target check point. Commonly used halogenating reagents such as iodine elementals are matched with appropriate oxidizing agents, or specific iodizing reagents can be used to achieve this step under mild conditions.
Then, the resulting iodine-containing methoxy benzene compound is subjected to difluoromethylation. This step can be achieved by various methods, such as the use of difluoromethylation reagents, such as difluoromethyl halides or active intermediates containing difluoromethyl. In the presence of suitable bases and catalysts, methoxy groups and difluoromethyl groups are substituted to form the key structure of 3- (difluoromethoxy) iodobenzene. During the reaction, the strength of the base, the type and amount of catalyst all have a significant impact on the efficiency and selectivity of the reaction, and need to be carefully regulated.
Another idea is to use iodine-containing benzene as the starting material, and introduce suitable functional groups first, so that difluoromethoxy groups can be introduced later. For example, iodobenzene is first functionalized to form an iodobenzene derivative with a convertible group. Subsequently, the difluoromethoxy group is connected by the reaction between the group and the difluoromethylation reagent. This approach requires detailed optimization of the conditions of each step of the reaction to ensure the smooth progress of each step and the purity of the product.
Furthermore, the positioning effect on the benzene ring can be exploited by designing a reasonable synthetic route. First, a group with positioning guidance is introduced to guide the introduction of iodine atoms and difluoromethoxy groups at the desired position. In the whole synthesis process, the separation and purification of the product after each step of the reaction is also crucial, and means such as column chromatography and recrystallization are often used to obtain high-purity 3- (difluoromethoxy) iodobenzene.

For 3 - (difluoromethoxy) iodobenzene, many things should be paid attention to during storage and transportation. The nature of this compound may be more active, and the first environment should be selected when storing. It should be placed in a cool, dry and well-ventilated place, away from hot topics and open flames, to prevent chemical reactions caused by temperature, fire, or even danger.
Packaging is also crucial. It needs to be packed with suitable packaging materials to ensure good sealing and prevent leakage. Because leakage not only damages materials, but also poses a risk of harm to the environment and people. If the packaging is damaged, it should be dealt with quickly without delay.
When transporting, also need to be cautious. The carrier should be clean, dry, and free of impurities that cause the reaction of this compound. During transportation, it is advisable to drive slowly and steadily to avoid severe vibration and collision, causing damage to the package or causing internal reactions.
In addition, people who handle and come into contact with this substance should be equipped with protective equipment, such as gloves, goggles, protective clothing, etc. Due to inadvertent contact, it may hurt the skin or eyes, and if inhaled or ingested, it may endanger health.
In addition, the records of its storage and transportation should not be ignored. Write down the storage time, quantity, storage conditions, etc. in detail for traceability and management. In this way, it is necessary to ensure the safety of 3 - (difluoromethoxy) iodobenzene during storage and transportation.

I don't know what the market value of "3 - (Difluoromethoxy) Iodobenzene" is. This compound is not easily available, and its market value is determined by many factors.
First, the ease of production is one of the main factors. If its synthesis requires a lot of steps, special raw materials or harsh reverse parts, the cost will be high, and the price will also be higher. Furthermore, the supply and demand of the market are large. If the demand is low, and the supply is limited, the price will rise; if the demand is low, the price may decline.
In addition, the cost also affects its cost. Those with high cost are usually higher than those with low cost due to high cost. In addition, different suppliers also have different prices. Different companies have different cost control and cost-effective strategies, and the results are different.
However, we have not yet obtained the market inspection, and we have not yet announced the price of the product. If you want to know the price, you can use the chemical raw material supplier, the chemical product trading platform, or the recent chemical market announcement to get the market.