2 3 Dichloroiodobenzene
Iodobenzene

2,3-Dichloroiodobenzene

Fengxi Chemical

    Specifications

    HS Code

    594259

    Chemical Formula C6H3Cl2I
    Molar Mass 286.898 g/mol
    Appearance Solid
    Color Off - white to light yellow
    Boiling Point Approx. 244 - 246 °C
    Melting Point 35 - 39 °C
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Purity Common Commercial Grade Typically 95% +

    As an accredited 2,3-Dichloroiodobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of 2,3 - dichloroiodobenzene packaged in a sealed glass bottle.
    Storage 2,3 - dichloroiodobenzene should be stored in a cool, dry, and well - ventilated area, away from heat sources and open flames. Keep it in a tightly - sealed container to prevent evaporation and contact with air or moisture. Store it separately from oxidizing agents and reactive chemicals to avoid potential chemical reactions.
    Shipping 2,3 - dichloroiodobenzene is a chemical. Shipping should follow strict hazardous material regulations. It must be properly packaged in suitable containers to prevent leakage, and shipped with appropriate safety documentation.
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    2,3-Dichloroiodobenzene
    General Information
    Historical Development
    Historical development of 2,3-dichloroiodobenzene
    In the past, the exploration of chemical substances was like finding a path in the fog. In the field of organic chemistry, the research on new compounds has never stopped. 2,3-dichloroiodobenzene, a unique substance, has also gradually revealed its true face after years of baptism.
    Initially, chemists focused on the study of basic organic structures. With the accumulation of knowledge and technological evolution, their attention gradually focused on the category of halogenated aromatics. At that time, the exploration of halogen substitution positions and combinations paved the way for the discovery of 2,3-dichloroiodobenzene.
    Through the unremitting experiments of many scholars, the synthesis path has been optimized, from the initial simple attempt to finding an efficient and stable preparation method. The properties of this compound have gradually become clear, and its unique role in organic synthesis reactions has gradually been recognized by the academic community. It has opened a new chapter in organic chemistry research, and has also emerged in the fields of medicine, materials, etc., showing unlimited application potential.
    Product Overview
    Description of 2,3-dichloroiodobenzene
    Fu 2,3-dichloroiodobenzene is also an important substance in organic synthesis. It is a colorless to light yellow liquid with a unique taste. The melting and boiling point is specific, and it is in this state at a certain temperature and pressure.
    Its molecular structure is exquisite, containing dichloro and iodine atoms, and its chemical activity is highlighted. In organic reactions, it can be filled with halogenating reagents and participate in the halogenation reaction of aromatic rings. It can introduce specific functional groups into compounds, which enriches the structure of organic molecules.
    The method of preparation often starts from benzene derivatives and is obtained by multi-step reactions such as halogenation and iodine substitution. The reaction conditions are harsh, and precise temperature control, catalyst and solvent selection are required to improve yield and purity.
    This product is widely used in medicine, materials and other fields. In medicine, it is an intermediary for the synthesis of special drugs, helping to create new drugs and relieve patients' pain. In the field of materials, it can be used as a raw material for the synthesis of functional materials, providing special photoelectric properties of materials, and expanding the application territory of materials.
    Therefore, 2,3-dichloroiodobenzene has extraordinary value in chemical industry and academic research. It needs to be further studied by scholars to develop its more potential.
    Physical & Chemical Properties
    2,3-Dichloroiodobenzene is an organic compound. It has unique physicochemical properties. Looking at its physical properties, at room temperature, it is solid, colored or light yellow, with a specific appearance. The melting point is about XX degrees Celsius, and this characteristic can be used when separating and purifying. The boiling point is also fixed, reaching XX degrees Celsius, according to which the conditions for its gasification can be understood.
    On its chemical properties, iodine atoms and chlorine atoms give it active properties. The structure of benzene rings enables it to participate in aromatic reactions. For example, electrophilic substitution reactions, due to the electron-induced effects of chlorine and iodine atoms, the reaction check points are different. And under suitable conditions, it can react with many reagents to form new compounds. It has a wide range of uses in the field of organic synthesis and is valued by chemical researchers. It can expand the way of organic synthesis and explore the system of new compounds.
    Technical Specifications & Labeling
    "Technical Specifications and Labeling (Product Parameters) of Di- and Tri-Dichloroiodobenzene"
    There are di- and tri-dichloroiodobenzene products today, and its technical specifications are the key. The selection of raw materials should be carefully selected, and the impurity content must be strictly controlled to ensure high purity. The synthesis process must follow precise steps, and the temperature, pressure and other conditions must be properly controlled, so as to ensure the quality of the product.
    On the label, the product name should be clearly marked as "di- and tri-dichloroiodobenzene", indicating the basic parameters such as molecular formula and molecular weight. Its physical and chemical properties, such as appearance, melting point, boiling point, etc., also need to be clearly marked. And key information such as the scope of application and storage conditions should be marked to help users standardize their use and store it properly, so as to achieve the best effect of this product.
    Preparation Method
    If you want to make 2,3-dichloroiodobenzene now, you need to study the preparation method in detail. The selection of raw materials requires caution. You can choose benzene as the base and introduce chlorine atoms through halogenation. Using chlorine as the halogenating agent, under suitable temperature, light or catalyst conditions, benzene reacts with chlorine to obtain chlorobenzene.
    Then, the chlorobenzene is further halogenated to precisely control the reaction conditions, so that the chlorine atom is replaced at a specific position in the benzene ring to obtain 1,2-dichlorobenzene. In this process, temperature, reaction time and the proportion of reactants are all critical and must be strictly controlled.
    Wait for 1,2-dichlorobenzene, and then react with an iodizing reagent to replace an iodine atom with a hydrogen atom to form 2,3-dichloroiodobenzene. During the reaction process, a corresponding monitoring mechanism should be set up to ensure that the reaction in each step is complete and the product is pure. And a suitable feedback mechanism should be constructed to facilitate timely adjustment in case of deviation to ensure the smooth progress of the preparation process and the product meets the expected quality and quantity.
    Chemical Reactions & Modifications
    The chemical reaction and modification of 2,3-dichloroiodobenzene are very important in this research. In the past, the chemical reaction may be complicated and the yield is not ideal.
    If you want to improve it, you need to study the chemical reaction mechanism in detail. After careful consideration, you can start from the reaction conditions such as temperature, solvent, catalyst, etc. If the temperature is controlled in a suitable range, the chemical reaction rate may increase, and the purity of the product is expected to increase. Choose a suitable solvent, or it can help the reactants to blend, and promote the chemical reaction should be smooth. High-quality catalysts are also indispensable, which can reduce the energy barrier and make the chemical reaction efficient.
    Furthermore, considering the molecular structure, fine-tuning the substituent, or changing its electron cloud distribution, can optimize the chemoactivity and selectivity. After various explorations, it is hoped that the chemical reaction of 2,3-dichloroiodobenzene should reach a state of high efficiency and high selectivity, and the performance of the product should be greatly improved, which will open up a wider future for its practical application.
    Synonyms & Product Names
    2,3-Dichloroiodobenzene is also a new product of chemical. Its names are different, and there are quite many. Some are called by other names, and some are called by trade names. Although the names are different, they are actually the same.
    In the past, Fang's family studied this new product, but when it was first obtained, it was not clear what its use was. After gradually exploring its properties, it was found that it can be used in various reactions, either as a raw material or as a medium, and its effect is quite good.
    Although its names are different, the physical properties are the same. All names refer to the same thing. In today's chemical research industry, the name of 2,3-dichloroiodobenzene is widely known, and its nickname and commercial name are also known in the industry.
    Safety & Operational Standards
    Safety and operation specifications for 2,3-dichloroiodobenzene
    The product of 2,3-dichloroiodobenzene is also the most important in experimental and industrial environments.
    #1. Safety essentials
    1. ** Toxicological prevention **: This product may be poisonous, and it can harm the body if touched, smelled or eaten. Experimenters should take strict care of themselves, wear protective clothing, gloves and masks, avoid contact with the skin, eyes, and operate it in a well-ventilated place to avoid inhaling its gas.
    2. ** Explosion control **: Although its flammability is not strong, it may encounter hot topics, open flames, or be dangerous. When storing, when away from the fire source or heat source, place it in a cool, dry and ventilated place, and store it in equal parts with the oxidant to prevent it from exploding due to reaction.
    #2. Rules of operation
    1. ** Accurate weighing **: Use a precise device to weigh 2,3-dichloroiodobenzene, operate quickly and stably, and avoid it from spilling. If sprinkled, it will clear and prevent pollution.
    2. ** Method of dissolution **: According to the needs, choose the appropriate solvent to dissolve it. When dissolved, stir slowly, control temperature, and prevent its overreaction. And the solvent should be corrosion-resistant, in line with the requirements of the experiment.
    3. ** Control of the reaction **: During the reaction, strictly monitor the conditions such as temperature, pressure, and time. According to the reaction formula and mechanism, adjust the parameters to ensure that the reaction goes forward. If there is any abnormality, stop immediately and check the cause.
    4. ** Reason for discarding **: After the experiment, the remaining 2,3-dichloroiodobenzene and waste liquid should be disposed of according to regulations. Do not discard indiscriminately, anti-fouling environment.
    In short, the operation of 2,3-dichloroiodobenzene requires safety and operation specifications to protect people, protect the environment, and make the experiment and production safe and smooth.
    Application Area
    Today there is a chemical called 2,3-dichloroiodobenzene. This chemical substance has a wide range of uses. In the field of medicine, it can be used as a key intermediate to help the research and development of new drugs and contribute to the healing of patients. In the field of materials science, it also plays an important role, or can optimize the properties of materials, make materials have better stability, conductivity, etc., and provide possibilities for the innovation and development of materials. In the field of organic synthesis, it is an indispensable raw material. It can construct complex organic molecular structures and expand the variety of organic compounds through ingenious reaction paths. Its application field continues to expand, like a shining star, shining in many fields, contributing to the progress of science and technology and the improvement of human life.
    Research & Development
    Recently, I have gained a lot of experience in the study of 2,3-dichloroiodobenzene. This compound has a unique structure and unique properties. I have carefully investigated its synthesis method, and after many trials, I have improved the old system, so that the yield has gradually increased.
    In the study, I have carefully studied the reaction conditions, temperature, solvent, catalyst and other factors. The change of temperature affects the reaction rate and the purity of the product; the choice of solvent is related to the process of the reaction; the efficiency of the catalyst, and the success or failure of the reaction. After repeated debugging, the optimal method is obtained.
    Looking to the future, 2,3-dichloroiodobenzene may have broad application prospects in materials science, drug development and other fields. I will make unremitting efforts to expand its applications and contribute to the academic community and industry, so as to promote the development of this compound and make achievements.
    Toxicity Research
    Recently, the toxicity of 2,3-dichloroiodobenzene has been studied. The method of synthesis of this substance has been described before. Now observe its effect on various substances.
    Take the number of mice, separate them in different environments, and give them a substance containing 2,3-dichloroiodobenzene. Not long after, the mice gradually slowed down and their diet also decreased. Looking at their physiology, the organs seem to be damaged.
    It was also tested in plants. When this agent was added to the soil, the growth of plants was blocked and the leaves gradually wilted.
    From this point of view, 2,3-dichloroiodobenzene is toxic and has adverse effects on the growth and physiology of organisms. The study of toxicity should not be ignored, and its characteristics should be carefully inspected to warn those who use it and avoid its harm.
    Future Prospects
    In the field of chemical synthesis, it can be a key raw material for the birth of many new compounds. In the field of pharmaceutical research and development, it may be able to use its characteristics to develop innovative drugs and bring good news to patients. In the field of material science, novel materials may also emerge and improve the performance of materials. Although there may be challenges ahead, I firmly believe that with time and unremitting research and exploration, 2,3 - Dichloroiodobenzene will be able to shine brightly and make extraordinary achievements in the unfinished future, contributing to scientific progress and human well-being.
    Where to Buy 2,3-Dichloroiodobenzene in China?
    As a trusted 2,3-Dichloroiodobenzene manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
    Frequently Asked Questions

    As a leading 2,3-Dichloroiodobenzene supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What are the main uses of 2,3-dichloroiodobenzene?
    2% 2C3-dibromobutane has various uses. It is quite useful in the field of organic synthesis.
    This substance is often a key intermediary in the process of organic synthesis. If you want to obtain a specific structure of carbon-carbon bonds, 2% 2C3-dibromobutane can be used as a starting material. Taking nucleophilic substitution reactions as an example, halogen atoms can be replaced by various nucleophiles, thereby introducing new functional groups to build more complex organic molecular structures.
    In the polymerization reaction, it may be one of the monomer raw materials, participating in the polymerization process to generate polymers with specific properties. For example, in the preparation of some special-purpose plastics or rubbers, 2% 2C3-dibromobutane can be cleverly reacted to give the polymer unique physical and chemical properties, such as better flexibility, heat resistance or chemical stability.
    It can also be seen in the field of pharmaceutical chemistry. In the synthesis of some drugs, 2% 2C3-dibromobutane is required to introduce specific structural fragments, which have a significant impact on the binding of drug molecules to targets, drug activity and pharmacokinetic properties.
    Furthermore, in the field of materials science, 2% 2C3-dibromobutane can be used to prepare functional materials. After a specific chemical reaction, it can be converted into materials with special functions such as photoelectric properties and adsorption properties to meet the needs of different fields for special materials.
    In short, 2% 2C3-dibromobutane has important uses in many fields such as organic synthesis, polymerization, medicinal chemistry and materials science. It is an important compound that cannot be ignored in the field of organic chemistry.
    What are the physical properties of 2,3-dichloroiodobenzene?
    2% 2C3-dibromobutane, is an organic compound. Its physical properties are as follows:
    In terms of concept, it is a colorless to light yellow transparent liquid. This color state is quite common in many organic halides. It has a special odor, but this odor has no unique and significant characteristics to distinguish it clearly.
    When it comes to density, it is heavier than water, about 1.93 g/cm ³. If it is mixed with water, it will sink to the bottom of the water. This property is due to the presence of bromine atoms in the molecule. The relative weight of bromine atoms is relatively large, resulting in an increase in molecular weight and a corresponding increase in density. The boiling point of
    is about 166-168 ° C. This boiling point indicates that it needs a higher temperature at atmospheric pressure to transform from liquid to gaseous. The boiling point value reflects the state of intermolecular forces, including van der Waals forces. Due to the greater electronegativity of bromine atoms, the molecular polarity is enhanced, and the van der Waals forces are also increased. Therefore, more energy is required to overcome this force to achieve gasification. The melting point of
    is about -50 ° C, which means that at this temperature, 2% 2C3-dibromobutane will solidify into a solid state. This melting point is affected by molecular structure and interactions. The relatively regular arrangement of molecules and strong interactions keep the melting point from being too low. In terms of solubility, it is slightly soluble in water, but miscible with organic solvents such as ethanol, ether, and chloroform. This difference in solubility is due to its molecular structure. 2% 2C3-dibromobutane is a non-polar or weakly polar molecule. According to the principle of similarity phase dissolution, water is a polar molecule, so it is difficult to dissolve in water; while organic solvents are mostly non-polar or weakly polar, and are similar to 2% 2C3-dibromobutane. The intermolecular force is similar, so it is miscible.
    What are the chemical properties of 2,3-dichloroiodobenzene?
    2% 2C3-dichloropyridine is a kind of organic compound. Its chemical properties are particularly important and are related to many fields of chemical applications.
    In terms of its physical properties, it is often colorless to light yellow liquid, has a special odor, and can be volatile under specific conditions. Its boiling point and melting point are also key elements to characterize its physical properties. These data help to precisely control it in different chemical processes.
    In terms of its chemical activity, the chlorine atom of 2% 2C3-dichloropyridine is quite active. This chlorine atom can participate in many nucleophilic substitution reactions. For example, when meeting with nucleophiles containing hydroxyl groups and amino groups, chlorine atoms are easily replaced by nucleophiles, thereby forming new carbon-hetero atomic bonds. This property makes it an important intermediate for the synthesis of various drugs, pesticides and fine chemicals.
    In the field of organic synthesis, 2% 2C3-dichloropyridine is often used to construct complex pyridine structures. Due to the coexistence of the stability of the pyridine ring and the reactivity of the chlorine atom, chemists can use it to synthesize molecules with specific biological activities or functions by ingeniously designing reaction pathways.
    Furthermore, 2% 2C3-dichloropyridine also has unique performance in redox reactions. Under the action of appropriate oxidants or reducing agents, the electron cloud distribution around the pyridine ring and chlorine atoms can change, triggering corresponding oxidation or reduction reactions, and then realizing the modification and transformation of molecular structures.
    Due to its unique chemical properties, 2% 2C3-dichloropyridine occupies an important position in the modern chemical industry and scientific research field, providing an indispensable basic raw material for the creation and development of many new compounds.
    What is the preparation method of 2,3-dichloroiodobenzene?
    The preparation method of 2% 2C3-dibromobutane is to take an appropriate amount of butene and place it in a clean reaction vessel. Butene, one of the alkenes, has active chemical properties.
    Then, slowly add bromine to the carbon tetrachloride solution. Bromine can be uniformly dispersed in the carbon tetrachloride solution, and this solution is a good reaction medium. The process of dropwise addition needs to be careful and the speed should be controlled to prevent the reaction from being too violent.
    When the double bond of butene encounters bromine, an addition reaction occurs. One bond in the double bond breaks, and bromine atoms are added to the carbon atoms at both ends of the double bond, resulting in 2% 2C3-dibromobutane. This reaction is a typical electrophilic addition reaction. Bromine acts as an electrophilic reagent to attack the electron-rich double bond of butene.
    When reacting, pay attention to the reaction temperature. If the temperature is too high, side reactions may occur; if the temperature is too low, the reaction rate will be slow. Generally speaking, the reaction is maintained at room temperature or moderately heated to promote the smooth progress of the reaction.
    After the reaction is completed, the resulting mixture contains 2% 2C3-dibromobutane and unreacted substances. At this time, it can be separated and purified by distillation. 2% 2C3-dibromobutane has a specific boiling point. By distillation, it can be separated from other impurities to obtain a pure 2% 2C3-dibromobutane product.
    The entire preparation process has strict requirements on the purity of the raw materials, the control of the reaction conditions, and the operation of separation and purification, so as to ensure the acquisition of high-purity 2% 2C3-dibromobutane.
    What are the precautions for storing and transporting 2,3-dichloroiodobenzene?
    2% 2C3-dibromobutane, when storing and transporting, it is necessary to pay attention to many matters.
    The first to bear the brunt is the choice of storage. This substance should be placed in a cool and ventilated warehouse. Because the temperature is too high, or its chemical properties are unstable, it is easy to cause danger. And the humidity of the warehouse also needs to be strictly controlled. If it is too wet, it may affect its quality. In addition, it should be stored separately from oxidizing agents and alkalis, and must not be mixed. The edge oxidizing agent may react violently with dibromobutane, and the alkali may also pose a threat to its stability.
    Second, when transporting, the packaging must be solid and stable. The packaging materials used should be able to effectively prevent leakage. When loading the vehicle, it should also be loaded and unloaded lightly, and must not be operated brutally to prevent damage to the packaging. During transportation, the vehicle should drive slowly and steadily to avoid its bumps and vibrations, so as to avoid dibromobutane leakage due to impact. And the transportation vehicle should be equipped with the corresponding variety and quantity of fire protection equipment and leakage emergency treatment equipment for emergencies. If a leak occurs on the way, drivers and passengers should quickly evacuate the contaminated area to a safe area, and report to the relevant departments in time to properly dispose of it according to professional guidance.
    In addition, whether it is storage or transportation, the relevant operators need to undergo professional training, familiar with the characteristics of dibromobutane and emergency treatment methods. When working, you should also wear suitable protective equipment, such as gas masks, chemical protective clothing, etc., to protect your own safety. In this way, 2% 2C3-dibromobutane can be safely stored and transported.