1 4 Dibromo 2 5 Diiodobenzene
Iodobenzene

1 4 Dibromo 2 5 Diiodobenzene

Fengxi Chemical

Specifications

HS Code

187470

Name 1,4 - dibromo - 2,5 - diiodobenzene
Chemical Formula C6H2Br2I2
Molar Mass 499.70 g/mol
Appearance Solid (usually white to off - white powder)
Physical State At Room Temperature Solid
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Melting Point 188 - 191 °C
Boiling Point Decomposes before boiling
Odor Odorless or very faint odor
Packing & Storage
Packing 100g of 1,4 - dibromo - 2,5 - diiodobenzene packaged in a sealed, chemical - resistant bottle.
Storage 1,4 - Dibromo - 2,5 - diiodobenzene should be stored in a cool, dry, and well - ventilated area, away from heat sources and direct sunlight. It should be kept in a tightly sealed container to prevent exposure to moisture and air, which could potentially cause degradation. Store it separately from oxidizing agents and other reactive chemicals to avoid unwanted reactions.
Shipping 1,4 - dibromo - 2,5 - diiodobenzene is shipped in well - sealed, corrosion - resistant containers. It's transported in accordance with hazardous chemical regulations, ensuring proper handling to prevent spills and maintain safety during transit.
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1,4-dibromo-2,5-diiodobenzene 1,4-dibromo-2,5-diiodobenzene 1,4-dibromo-2,5-diiodobenzene
General Information
Frequently Asked Questions
What are the main uses of 1,4-dibromo-2,5-diiodobenzene?
1% 2C4-dibromo-2% 2C5-dichlorobenzene is a key organic halide in the current organic synthesis field. It has a wide range of main uses and plays an important role in pesticides, medicine, materials and other industries.
In the field of pesticides, 1% 2C4-dibromo-2% 2C5-dichlorobenzene is a key intermediate for the synthesis of specific high-efficiency insecticides and fungicides. Due to its unique chemical structure, it can be connected to the main chain of pesticide molecules through specific chemical reaction steps, giving pesticides better biological activity and stability. For example, through a series of reactions, it is converted into a new type of insecticide containing this structure, which interferes with the nerve conduction of specific pests, enhances the insecticidal effect, and reduces the impact on beneficial organisms in the environment, improving the selectivity and safety of pesticides.
In the pharmaceutical industry, 1% 2C4-dibromo-2% 2C5-dichlorobenzene is also an important starting material for the synthesis of some drugs. Studies have found that its halobenzene structure can be used as a key component of drug active groups and interact with specific human targets. For example, in the development of some anti-tumor drugs, complex drug molecular structures are constructed on this basis, and their structural properties bind to specific proteins or enzymes in tumor cells to inhibit tumor cell growth and proliferation, providing a key material basis for the development of new anti-cancer drugs.
In the field of materials science, 1% 2C4-dibromo-2% 2C5-dichlorobenzene is often used to synthesize high-performance polymer materials. As a reaction monomer, it can be polymerized with other compounds containing specific functional groups to prepare polymer materials with excellent thermal stability, mechanical properties and electrical properties. Such materials are widely used in high-end fields such as electronics, appliances, aerospace, etc. For example, when used in electronic packaging materials, its excellent thermal stability and insulation properties can protect electronic components from operating stably in harsh environments such as high temperature and high humidity, thus enhancing the reliability and service life of electronic devices.
What are the synthesis methods of 1,4-dibromo-2,5-diiodobenzene?
The synthesis of 1% 2C4-dibromo-2% 2C5-dichlorobenzene is an important topic in the field of organic synthesis. There are many ways to synthesize it, and the common ones are as follows:
First, benzene is used as the starting material, and bromine and chlorine atoms are gradually introduced by halogenation reaction. First, benzene and bromine are brominated under the action of catalysts such as iron or iron tribromide to generate bromobenzene. In this reaction, the bromine molecule is polarized under the action of the catalyst, and the electrophilic bromine positive ion attacks the benzene ring, and through a series of intermediate steps, bromobenzene is generated. Then, the bromobenzene is chlorinated, and 1-bromo-4-chlorobenzene can be obtained by introducing chlorine gas in the presence of suitable catalysts such as ferric chloride. Finally, under specific conditions, the bromide and chlorine are again substituted to achieve the synthesis of 1% 2C4-dibromo-2% 2C5-dichlorobenzene.
Second, p-dichlorobenzene or p-dibromobenzene can also be selected as raw materials. If p-dichlorobenzene is used as the starting material, it can be reacted with bromine sources such as N-bromosuccinimide (NBS) in a suitable solvent and catalyst system. NBS can provide bromine radicals. Under the action of light or initiator, the radical substitution reaction is initiated, and the bromine atom is gradually introduced into the specific position of the benzene ring to obtain the target product. Similarly, using p-dibromobenzene as raw material, using suitable chlorination reagents, such as chlorine gas or thionyl chloride, under suitable conditions, the chlorination reaction can also synthesize 1% 2C4-dibromo-2% 2C5-dichlorobenzene.
Third, using the Grignard reagent method. First prepare Grignard reagents containing bromine or chlorine, such as Grignard reagents made of bromobenzene, and chlorine-containing halogenated hydrocarbons or vice versa, in anhydrous ether or tetrahydrofuran and other solvents, through Grignard reaction to form carbon-carbon bonds, and then through subsequent treatment, to achieve the precise positioning of bromine and chlorine atoms on the benzene ring, and finally synthesize 1% 2C4-dibromo-2% 2C5-dichlorobenzene.
These many synthesis methods have their own advantages and disadvantages, and the appropriate method should be carefully selected according to actual needs, considering factors such as raw material cost, reaction conditions, yield and product purity.
What are the physical properties of 1,4-dibromo-2,5-diiodobenzene?
1% 2C4-dibromo-2% 2C5-dichlorobenzene is a kind of organic compound. Its physical properties are as follows:
Under normal temperature and pressure, it often takes the form of white to light yellow crystalline powder, which is easy to identify and process. Regarding the melting point, it is between 138 and 141 degrees Celsius. The characteristics of the melting point are of great significance in the separation, purification and identification of substances. The boiling point is about 282-284 degrees Celsius. The value of the boiling point is related to the phase change during the heating process. It is also important to pay attention to the chemical production and experimental operation. < Br >
Its density is about 1.94 g/cm ³. This density data is crucial for the measurement, mixing, and distribution of materials in different media. As for solubility, the substance is insoluble in water, but soluble in organic solvents such as ethanol, ether, and acetone. This difference in solubility has a significant impact on the extraction of the substance and the selection of the reaction medium.
And it has a certain stability. Under normal conditions, the chemical properties are relatively calm, and it is not easy to spontaneously produce violent chemical reactions. When exposed to high temperatures, open flames, or strong oxidizing agents, there are also certain risks, or dangerous reactions such as combustion and explosion may occur. Therefore, when storing and using, strict safety procedures should be followed to prevent unexpected changes.
Is the chemical properties of 1,4-dibromo-2,5-diiodobenzene stable?
The chemical properties of 1% 2C4-dibromo-2% 2C5-dichlorobenzene are quite stable. In this compound, bromine and chlorine atoms are closely connected to the benzene ring through covalent bonds. The structure of the benzene ring itself is highly stable, and the existence of the conjugated system makes the electron cloud uniformly distributed, thereby enhancing the overall stability of the molecule.
Bromine and chlorine atoms are both elements with high electronegativity. In this compound, they reduce the electron cloud density of the benzene ring by virtue of their electron-withdrawing induction effect. However, this electron-withdrawing effect does not cause significant damage to the conjugated system of the benzene ring, but makes the molecular structure more stable.
Furthermore, the carbon-bromine and carbon-chlorine bond energies are relatively high, and in order to break them, sufficient energy needs to be supplied. Under normal conditions, external energy is difficult to meet this demand, because the chemical properties of the compound are stable. In general chemical reaction environments, 1% 2C4-dibromo-2% 2C5-dichlorobenzene is not easy to react with other substances, and can maintain its own structure and properties unchanged in a certain period of time and environment. Even under relatively mild chemical reaction conditions, it is difficult to see its chemical changes easily, which proves its high stability.
What is the price range of 1,4-dibromo-2,5-diiodobenzene in the market?
For 1% 2C4-dibromo-2% 2C5-dichlorobenzene, it is difficult to determine the price range in the market. The price is influenced by many factors.
First, the situation of supply and demand is the main reason. If there are many people who want it, but the supply is small, the price will increase; conversely, if the supply exceeds the demand, the price may decrease. Second, the price of raw materials also has a great impact. If the price of raw materials required for the preparation of this substance rises, the price of the finished product will also rise; if the price of raw materials falls, the price of the finished product may decrease. Furthermore, the technology and cost of production are also crucial. If there is an advanced technique that can reduce the consumption of production and reduce costs, the price may be more competitive; if the technique is old and the cost is high, the price will be difficult to lower.
In addition, the competitive situation of the market also affects its price. If there is competition in the same industry, it is for market share, or there is a reduction in the price to seek; if the market monopoly is high, the pricing power is in the minority, and the price may be high. In addition, differences in regions and seasons can make the price fluctuate. Therefore, in order to determine its price range, it is necessary to consider various factors in detail and observe it in real time to obtain a more accurate number. Generally speaking, in the current complex state of the market, its price range is difficult to hide, and it must be analyzed according to the situation.