2 Iodo 5 Bromobenzyl Chloride
Iodobenzene

2-iodo-5-bromobenzyl Chloride

Fengxi Chemical

Specifications

HS Code

643757

Chemical Formula C7H5BrClI
Molecular Weight 329.38
Appearance Typically a solid (description may vary based on purity and conditions)
Physical State At Room Temperature Solid
Solubility In Water Insoluble (organic halide, non - polar nature)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Vapor Pressure Very low (due to being a solid at room temperature)
Chemical Formula C7H5BrClI
Molecular Weight 329.38
Appearance Typically a solid
Solubility In Water Low solubility (organic halide nature)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Hazard Class Irritant, potentially harmful due to halogen content
Chemical Formula C7H5BrClI
Molecular Weight 329.38
Appearance Typically a solid
Melting Point Varies, needs experimental determination
Solubility In Water Low solubility in water
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane
Density Data requires experimental measurement
Flash Point Experimental determination needed
Hazard Class Irritant, potential health risks
Chemical Formula C7H5BrClI
Molecular Weight 329.38
Appearance Solid (usually)
Melting Point Data needed
Boiling Point Data needed
Density Data needed
Solubility In Water Low
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane
Flash Point Data needed
Hazard Class Corrosive, Toxic (iodine, bromine, chlorine - containing, may be harmful if inhaled, ingested or through skin contact)
Cas Number Data needed
Purity Varies by manufacturer
Chemical Formula C7H5BrClI
Molecular Weight 329.38
Appearance Typically a solid
Physical State At Room Temp Solid
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Odor Pungent, likely halogen - like odor
Stability Unstable under certain conditions, especially in the presence of nucleophiles
Reactivity Highly reactive due to the presence of multiple halogens, can undergo substitution reactions
Halogen Content Contains bromine, chlorine, and iodine
Packing & Storage
Packing 100g of 2 - iodo - 5 - bromobenzyl chloride packaged in a sealed, corrosion - resistant container.
Storage 2 - iodo - 5 - bromobenzyl chloride should be stored in a cool, dry, well - ventilated area away from heat sources and open flames. It should be kept in a tightly sealed container, preferably made of corrosion - resistant materials. Due to its reactivity, store it separately from incompatible substances like oxidizing agents, bases, and reducing agents to prevent potential chemical reactions and ensure safety.
Shipping 2 - iodo - 5 - bromobenzyl Chloride is a chemical. Shipping should be in accordance with strict hazardous materials regulations. It must be properly packaged to prevent leakage, and transported by carriers approved for such chemicals.
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2-iodo-5-bromobenzyl Chloride 2-iodo-5-bromobenzyl Chloride 2-iodo-5-bromobenzyl Chloride
General Information
Frequently Asked Questions
What is the chemistry of 2-iodo-5-bromobenzyl Chloride?
2-Iodine-5-bromobenzyl chloride, this is an organic compound. Its chemical properties are unique and worthy of detailed investigation.
Let's talk about the characteristics of halogen atoms first. The compound contains three halogen atoms of iodine, bromine and chlorine, and the activities of halogen atoms are different. Generally speaking, halogen atoms are affected by benzene ring and benzyl group, and the reactivity changes. Chlorine atoms are connected to benzyl groups. Due to the stability of benzyl carbon positive ions, the chlorine atoms in benzyl chloride are relatively active and prone to nucleophilic substitution reactions. Nucleophilic reagents such as alcohols, amines, mercaptan, etc., can attack benzyl carbon, and the chlorine atoms leave to form new compounds.
Iodine and bromine are attached to the benzene ring. Although the benzene ring is a conjugated system, the activity of the halogen atom is lower than that of the chlorine atom in the benzyl chloride, under certain conditions, it can still participate in the reaction. For example, in the nucleophilic aromatic substitution reaction, if there is an electron-absorbing group activation on the benzene ring, the iodine and bromine atoms can also be replaced by nucleophilic reagents. And the iodine atom is relatively large, and the electron cloud is easily polarized, sometimes making the reaction activity at the location different from the bromine atom.
Let's talk about its chemical stability. Due to the presence of multiple halogen atoms, the chemical stability of the compound is poor. When irradiated or heated, the halogen When storing and using, care should be taken to avoid conditions such as light and high temperature to prevent the compound from decomposing or unnecessary reactions.
In terms of solubility, in view of the halogen atom and benzyl group, the compound has a certain solubility in organic solvents such as dichloromethane, chloroform, and ether. Due to the principle of similarity and miscibility, these organic solvents have certain similarities with the compound structure and can interact with it. However, the solubility in water is low. Because it is an organic halide, it has a large polar difference with water and is not easy to form hydrogen bonds and other interactions.
In chemical reactions, 2-iodine-5-bromobenzyl chloride can be used as an important intermediate. Using the reactivity of halogen atoms, various complex organic compounds can be synthesized through different reaction paths, which has important application value in the field of organic synthesis.
What are the main uses of 2-iodo-5-bromobenzyl Chloride?
2-Iodo-5-bromobenzyl Chloride, which is 2-iodo-5-bromobenzyl chloride, has a wide range of uses.
In the field of organic synthesis, it is often a key intermediate. Because of its molecular structure, it contains halogen atoms, which are highly active and can participate in various chemical reactions. For example, in nucleophilic substitution reactions, the chlorine atom of benzyl chloride is very active and can be replaced by many nucleophiles. In the case of hydroxyl-containing nucleophiles, such as alcohols, under suitable conditions, the chlorine atom can be replaced by an oxy group to form corresponding ether compounds, which is of great significance for the preparation of ether substances.
Furthermore, iodine and bromine atoms can also play a key role in the construction of complex organic molecular structures. Through metal-catalyzed coupling reactions, such as palladium-catalyzed coupling reactions, iodine or bromine atoms can be coupled with other organic halides or organometallic reagents to realize the construction of carbon-carbon bonds, and assist in the synthesis of aromatic compounds with complex structures. In the field of medicinal chemistry, it has made a lot of contributions to the development of new drug molecular structures.
In the field of materials science, compounds synthesized from this raw material may have special optoelectronic properties. Due to its structural properties, or as a precursor of organic semiconductor materials, the materials prepared by subsequent reactions may exhibit unique electrical and optical properties in organic Light Emitting Diode (OLED), organic solar cells and other devices, providing possibilities for the development of new materials.
In addition, in the preparation of fine chemical products, 2-iodine-5-bromobenzyl chloride can be used to synthesize surfactants, fragrances and additives with special functions. Due to its unique chemical structure, the synthesized products may have special properties and application effects to meet the needs of different industrial fields.
What are the synthesis methods of 2-iodo-5-bromobenzyl Chloride?
The synthesis method of 2-iodine-5-bromobenzyl chloride is quite complicated, and it needs to be done step by step according to chemical principles.
One method is to use benzene as the starting material first. Benzene and bromine are electrophilically substituted under the action of catalysts such as iron bromide to obtain bromobenzene. In this reaction, iron bromide catalyzes the isocleavage of bromine molecules into bromine positive ions, which attack the benzene ring and replace the hydrogen on the benzene ring. After a series of electron transfers, bromobenzene is finally obtained.
Then, under appropriate conditions, p-bromobenzene and iodine are iodized with the help of certain catalysts and ligands. This process requires controlling the reaction temperature, time and other conditions, so that the iodine atom selectively replaces the hydrogen at a specific position on the bromobenzene to obtain 2-iodine-5-bromobenzene.
Then make 2-iodine-5-bromobenzene with formaldehyde, hydrogen chloride and other reagents in the presence of specific catalysts such as anhydrous zinc chloride. This reaction mechanism is more complex. Anhydrous zinc chloride promotes the formation of active chloromethyl cations between formaldehyde and hydrogen chloride, which attack the benzene ring of 2-iodine-5-bromobenzene. After electrophilic substitution, chloromethyl is introduced into the benzene ring, and then 2-iodine-5-bromobenzyl chloride is obtained.
There are other methods. 2-Iodo-5-bromobenzoic acid can be obtained by selectively introducing bromine and iodine atoms on the benzene ring through a halogenation reaction with benzoic acid as the starting material. Subsequently, 2-iodo-5-bromobenzoic acid is reduced by a reduction reaction, such as a strong reducing agent such as lithium aluminum hydride, and the carboxyl group is reduced to hydroxymethyl to obtain 2-iodo-5-bromobenzyl alcohol. Finally, 2-iodo-5-bromobenzyl chloride can also be obtained by the reaction of 2-iodo-5-bromobenzyl alcohol with chlorinated reagents such as sulfoxide chloride. When sulfoxide chloride reacts with alcohol, the intermediate product chlorosulfite is formed, which is then decomposed, and the chlorine atom replaces the hydroxyl group, releasing sulfur dioxide and hydrogen chloride
All synthesis methods have their own advantages and disadvantages. It is necessary to comprehensively consider many factors such as the availability of raw materials, the difficulty of reaction conditions, the level of yield and the impact on the environment, and choose the best one.
What are the precautions for 2-iodo-5-bromobenzyl Chloride during storage and transportation?
2-Iodine-5-bromobenzyl chloride This product needs to pay attention to many key matters during storage and transportation.
The choice of the first environment. It should be placed in a cool, dry and well-ventilated place, away from direct light and hot topics. Due to the chemical reaction between light and high temperature or the promotion of it, the properties are changed, the quality is affected, and even the danger is caused.
The second time and the firmness of the packaging. The packaging must be tight and firm to prevent leakage. In view of its certain chemical activity, after leakage or reaction with surrounding substances, it will pollute the environment and endanger personal safety. Choose suitable containers, such as glass bottles or special plastic containers, and ensure that they are sealed.
Furthermore, the storage should be separated from other chemicals. Because of its contact with certain substances, or violent reactions, it can cause serious accidents such as explosions and fires. In particular, keep away from oxidants, strong alkalis, and strong acidic substances to avoid interaction and cause disasters.
When transporting, follow strict regulations. Transportation vehicles need to be equipped with corresponding emergency treatment equipment and protective equipment for emergencies. Transport personnel should also be professionally trained to be familiar with the characteristics of the chemical and emergency treatment methods to ensure the safety of the whole transportation process.
In conclusion, 2-iodine-5-bromobenzyl chloride must be stored and transported with caution in terms of environment, packaging, chemical isolation, and personnel operation, and must not be negligent in order to ensure its safety and stability.
What is the market price of 2-iodo-5-bromobenzyl Chloride?
I think what you are asking is about the market price of 2-iodo-5-bromobenzyl Chloride. However, the price of this product is difficult to determine quickly. The price of the cover often changes due to various factors.
First, the price of raw materials has a great impact. If the price of raw materials such as iodine and bromine fluctuates, the cost of 2-iodo-5-bromobenzyl Chloride will change accordingly, and its price will also be different. If the raw material is expensive, the price of this compound will also be high; if the price of raw materials decreases, the price may also decrease.
Second, the technique of production is also the key. Sophisticated production technology can increase output, reduce costs, and make prices more competitive. If the production method is backward, the cost will be high, and the price will be difficult to lower.
Third, the supply and demand of the market determines the price. If the demand is strong and the supply is insufficient, the price will rise; if the market is saturated, the demand is weak, and the price may fall.
Fourth, factors such as origin and quality also play a role. Products of different origins, due to differences in environment and craftsmanship, may have different quality and different prices. High quality, the price is often higher than ordinary.
Therefore, in order to know the exact market price of 2-iodo-5-bromobenzyl Chloride, it is necessary to carefully observe the raw material market, production process, supply and demand situation and product quality, and to keep an eye on market changes at any time, in order to obtain a more accurate price.