M Diiodoperfluorobenzene
Iodobenzene

M Diiodoperfluorobenzene

Fengxi Chemical

Specifications

HS Code

857966

Packing & Storage
Packing 500g of M - diiodoperfluorobenzene packaged in a sealed, chemical - resistant bottle.
Storage M - diiodoperfluorobenzene should be stored in a cool, dry, well - ventilated area away from heat sources and open flames. Keep it in a tightly sealed container to prevent contact with air and moisture, which could potentially cause decomposition or reactivity issues. Store it separately from incompatible substances like oxidizing agents.
Shipping M - diiodoperfluorobenzene is shipped in specialized, tightly - sealed containers compliant with chemical transport regulations. Packaging ensures protection from external factors during transit to prevent spills and maintain chemical integrity.
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M-diiodoperfluorobenzene M-diiodoperfluorobenzene M-diiodoperfluorobenzene
General Information
Frequently Asked Questions
What are the main uses of M-diiodoperfluorobenzene?
M-diiodoperfluorobenzene is also an organic compound. It has a wide range of uses and is useful in various fields of chemical industry.
One can be used as a synthetic raw material for special materials in the field of materials science. With its fluorine and iodine properties, polymer materials with unique properties can be prepared through specific chemical reactions. These materials may have excellent chemical stability and resistance to strong acid and alkali erosion; or have good thermal stability and can maintain stable performance in high temperature environments. They can be widely used in industries such as aerospace and electronics that require strict material properties.
Both also have potential value in the field of medicinal chemistry. Because of their unique structure, they may be used as structural units of lead compounds. Chemists can explore new bioactive compounds by modifying their structures, providing a possible path for the development of new drugs. For example, by introducing specific functional groups and changing their interactions with biological targets, potential drug molecules can be screened.
The three are important intermediates in the field of organic synthesis chemistry. They can participate in a variety of organic reactions, such as palladium-catalyzed coupling reactions. Through these reactions, complex organic molecular structures can be constructed, the types and functions of organic compounds can be expanded, and the development of organic synthesis chemistry can be promoted, laying the foundation for the preparation of various fine chemicals.
What are the physical properties of M-diiodoperfluorobenzene?
M-diiodoperfluorobenzene has various physical properties. In terms of its color state, it is often a colorless to slightly yellow liquid. It is clear and transparent, like a clear Li, with a certain fluidity.
When it comes to the melting point, it is about -20 ° C. At this temperature, the material begins to change its phase state, like the gradual melting of ice in a cold day. Its boiling point is about 210-212 ° C. When it reaches this heat, it is like boiling water in a kettle and turns into a gaseous state.
The density is related to the ratio of mass to volume. The density of this material is quite large, about 2.6-2.7g/cm ³, which is heavier than that of common liquids. It is as if it contains more matter in the same volume.
In terms of solubility, it is soluble in organic solvents such as halogenated hydrocarbons and aromatic hydrocarbons. It is like salt entering water, and the phase is fused seamlessly, but it is difficult to dissolve in water. If oil floats in water, it is distinct.
Its vapor pressure is low at room temperature, that is, its tendency to volatilize is weak, and it is like a quiet thing, which does not easily disperse in the air. Surface tension also has its own specific value, which affects the interaction between liquids and interfaces, and is related to its spread on the solid surface. These physical properties have a crucial impact on the application of many fields such as chemicals and materials.
What is the chemistry of M-diiodoperfluorobenzene?
The chemical properties of M-diiodoperfluorobenzene are particularly important. This compound contains fluorine and iodine atoms. Due to the strong electronegativity of fluorine atoms, the molecule has a unique electron cloud distribution, which makes its chemical activity unusual.
In terms of its reactivity, the iodine atoms on the aromatic ring can participate in many nucleophilic substitution reactions. Due to the strong electron absorption of fluorine atoms, the electron cloud density of the benzene ring is reduced, and the carbon sites attached to the iodine atoms are more positively charged, and the nucleophilic reagents are easy to attack. However, the reaction conditions are harsher, and suitable catalysts and solvents are required. For example, taking the nucleophilic reagent alcohols as an example, under the catalysis of bases, substitution may occur, and ether In terms of stability, the overall stability of the molecule is quite good due to the high carbon-fluorine bond energy. Under common environmental conditions, it is difficult to decompose spontaneously or react with weakly active substances. In case of strong oxidizing agents or reducing agents, it can still react under specific conditions. Strong reducing agents or cause partial removal of fluorine atoms, or reduce iodine atoms to low-priced states.
In terms of solubility, in view of its polyfluorine structure, it has a certain lipid solubility and may have good solubility in organic solvents such as dichloromethane and chloroform, but it has poor solubility in water. Due to the large difference between molecular polarity and water.
M-diiodoperfluorobenzene has potential applications in organic synthesis, materials science and other fields due to its unique chemical properties. It can be used as an intermediate to prepare compounds and materials with special properties.
What is M-diiodoperfluorobenzene synthesis method?
The synthesis of M-diiodoperfluorobenzene is an important topic in organic synthetic chemistry. To prepare this compound, several routes are often followed.
First, perfluorobenzene is used as the starting material and iodine atoms are introduced through halogenation reaction. This halogenation reaction often requires specific halogenation reagents and reaction conditions. For example, iodine elemental substance can be selected to react with an appropriate catalyst in a suitable solvent. The choice of catalyst is crucial, such as some metal halide catalysts, which can promote the electrophilic substitution of iodine atoms to perfluorobenzene rings. During the reaction, conditions such as temperature and reaction time need to be strictly controlled to ensure that the reaction proceeds in the direction of generating M-diiodoperfluorobenzene and avoid over-halogenation or formation of other by-products.
Second, it can be achieved by the stepwise functional conversion of fluoroaromatic hydrocarbons. First, fluoroaromatic hydrocarbons are functionally specific, and groups that can be converted into iodine atoms are introduced, and then they are converted into iodine atoms through subsequent reactions. This method requires careful design of reaction steps. Each step requires mild conditions and good yield to ensure the efficiency and purity of the overall synthesis. After each step of the reaction, separation and purification operations, such as column chromatography, recrystallization, etc. are often required to remove impurities and ensure the purity of the intermediate product and the final product.
Or, a coupling reaction catalyzed by transition metals can be used. The coupling of fluorohalogenated aromatics with iodine substitutes occurs under the action of transition metal catalysts. Complexes of transition metal catalysts such as palladium and nickel can effectively promote the activation and coupling process of carbon-halogen bonds. Factors such as ligand, type and amount of base in the reaction system have a significant impact on the selectivity and yield of the reaction. Reasonable regulation of these factors and optimization of reaction conditions can efficiently synthesize M-diiodoperfluorobenzene. In short, the synthesis of M-diiodoperfluorobenzene requires comprehensive consideration of many factors such as starting materials, reaction reagents, catalysts, reaction conditions, separation and purification, and carefully designed synthesis routes to obtain ideal synthesis results.
What is the price range of M-diiodoperfluorobenzene in the market?
This compound is a benzene series containing fluorine and iodine, and its price is different due to a variety of factors.
First, the price of raw materials is the main factor. The production of this product requires specific fluorine and iodine-containing raw materials. If the raw materials are rare or difficult to make, the cost will rise, and the market price will also be high.
Second, the preparation method is difficult and difficult. If the synthesis method is complex, it needs high strips and special equipment, and the yield is low, and it requires more manpower and material resources, its price will increase.
Third, the supply and demand situation has a great impact. If there are many people who need this product, but there are few products, the supply is in short supply, and the price will tend to be higher; on the contrary, if the market supply exceeds the demand, the price may drop.
Fourth, the purity also involves the price. High-purity M-diiodoperfluorobenzene is more difficult to make, and the price should be higher than that of low purity.
Due to the above reasons, the price of M-diiodoperfluorobenzene is difficult to determine, and there may be a large price difference in the market. Buyers need to compare products of different origins and purity in detail to measure their price.