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3-Bromo-4-Fluoroiodobenzene

3-Bromo-4-Fluoroiodobenzene

Hongda Chemical

    Specifications

    HS Code

    699860

    Name 3-Bromo-4-Fluoroiodobenzene
    Molecular Formula C6H3BrFI
    Molecular Weight 300.89
    Cas Number 102875-52-1
    Appearance Colorless to light yellow liquid
    Boiling Point 226 - 228 °C
    Density 2.355 g/cm³
    Flash Point 101.2±23.2 °C
    Refractive Index 1.647
    Solubility Soluble in organic solvents like dichloromethane, chloroform

    As an accredited 3-Bromo-4-Fluoroiodobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of 3 - bromo - 4 - fluoroiodobenzene packaged in a sealed glass bottle.
    Storage 3 - Bromo - 4 - fluoroiodobenzene 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 vapor leakage. As it is a chemical, store it separately from oxidizing agents, reducing agents, and other incompatible substances to avoid potential reactions. Protect from direct sunlight.
    Shipping 3 - bromo - 4 - fluoroiodobenzene is shipped in sealed, specialized containers designed for hazardous chemicals. Packaging ensures protection from external factors. Shipment follows strict regulations for safe transportation of such chemicals.
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    3-Bromo-4-Fluoroiodobenzene 3-Bromo-4-Fluoroiodobenzene
    General Information
    Historical Development
    3 - Bromo - 4 - Fluoroiodobenzene is an organic compound whose historical development is quite interesting. In the past, organic chemistry was still in its infancy, and chemists dedicated themselves to exploring the synthesis and properties of various substances. At that time, research on such halogenated aromatics was gradually emerging.
    At first, the synthesis of this compound was quite difficult, due to the need to precisely control the reaction conditions and reagent ratios. However, chemists continued to study and improve the synthesis method. Over time, many new technologies have emerged, making the synthesis of 3 - Bromo - 4 - Fluoroiodobenzene more efficient and accurate.
    This compound is of great significance in the field of organic synthesis. Its development process has witnessed the evolution of chemical synthesis technology, laying the foundation for the subsequent synthesis of more complex organic compounds, and also promoting the continuous development of the field of organic chemistry.
    Product Overview
    Today there is a substance called 3 - Bromo - 4 - Fluoroiodobenzene. This is an organic compound with a unique structure. It is based on a benzene ring and is connected to atoms of bromine, fluorine, and iodine. The bromine atom is at the third position of the benzene ring, the fluorine atom is at the fourth position, and the iodine atom is also connected to the benzene ring. The three are in their own positions to construct a unique molecular structure.
    This substance has special properties and is quite useful in the field of organic synthesis. Due to its halogen-containing atoms, it can lead to a variety of chemical reactions, such as nucleophilic substitution reactions. Halogen atoms can be replaced by nucleophilic reagents, and then other organic compounds can be derived, which adds to organic synthesis and helps chemists expand the synthesis path. Preparation of many organic materials with special properties and uses may make outstanding contributions in the fields of medicine, materials science, etc.
    Physical & Chemical Properties
    3 - Bromo - 4 - Fluoroiodobenzene is an organic compound. Its physical properties are solid at room temperature, its color is close to white, and it has a slightly special smell. The melting point is within a certain range, which is determined by the intermolecular force. Its density also has a specific value, which is related to its material structure.
    In terms of its chemical properties, it is chemically active because it contains halogen atoms such as bromine, fluorine, and iodine. When encountering nucleophiles, halogen atoms are easily replaced, and halogen atoms have a certain electronegativity, which changes the density of electron clouds in the benzene ring. If it is co-heated with basic reagents, a nucleophilic substitution reaction can occur, and halogen atoms are replaced by other groups. And because the benzene ring conjugated system can participate in many aromatic-specific reactions, it is widely used in the field of organic synthesis and is an important intermediate for the preparation of complex organic compounds.
    Technical Specifications & Labeling
    Today there is a thing called 3 - Bromo - 4 - Fluoroiodobenzene. To clarify its technical specifications and labels (commodity parameters), it is necessary to investigate in detail.
    To observe this substance, it is necessary to observe its chemical structure, the arrangement and combination of atoms, and its characteristics. The location of its bromine (Bromo), fluorine (Fluoro) and iodine (iodo) is the key. In terms of technical specifications, purity is crucial, and the amount of impurities should not be careless. It should be ensured that its content reaches a specific standard before it can meet the needs of the user.
    In terms of identification, in addition to clearly writing its name, its physical and chemical properties need to be clarified. Such as melting point and boiling point, it is related to its storage and use conditions. And it must be marked with a safety warning, because it may be dangerous. In this way, only those who operate this thing can know its details, use it correctly, and ensure safety and achieve the purpose.
    Preparation Method
    3 - Bromo - 4 - Fluoroiodobenzene is an important organic synthesis intermediate, and its preparation method is as follows:
    In terms of raw materials, 4 - fluoroaniline is used as the starting material and is prepared by diazotization, halogen substitution and other reactions. In the synthesis process, 4 - fluoroaniline is first reacted with hydrochloric acid and sodium nitrite at low temperature to generate a diazonium salt. Subsequently, the diazonium salt is reacted with a mixed solution of cuprous bromide and potassium iodide to achieve halogen substitution, thereby introducing bromine atoms and iodine atoms. The reaction steps are in sequence, low temperature diazotization ensures the stable generation of diazonium salts, and then reacts with halogenated salts at appropriate temperatures to improve the reaction conversion rate. Optimizing reaction conditions, such as precise control of reaction temperature and material ratio, can improve yield and purity. Through this preparation process, the target product 3-Bromo-4-Fluoroiodobenzene can be obtained to meet the needs of organic synthesis.
    Chemical Reactions & Modifications
    I tried to study this chemical 3 - Bromo - 4 - Fluoroiodobenzene. Its chemical reaction is wonderful, related to many variables. At first, it was applied according to the usual method, but the effect was not as expected. Think about the reason, or the temperature and pressure of the environment are not appropriate, or the amount of catalyst is not right.
    Then change it, adjust the temperature to an appropriate level, increase the catalyst a little, and try again. It was seen that the speed increased greatly, and the yield also increased. This sincerity should be variable. Thinking about its nature, the atoms of bromine, fluorine and iodine in 3 - Bromo - 4 - Fluoroiodobenzene show their own characteristics and affect each other. The electronegativity of fluorine is strong, which causes the density of the electron cloud of the benzene ring to change, and its position is different from that of the electrophilic. After many tests, it is shown that the law of its transformation can be the basis for subsequent research and use, and the understanding should not be static.
    Synonyms & Product Names
    Today there is a thing called 3 - Bromo - 4 - Fluoroiodobenzene. This thing is of great significance in the field of my chemical research. Its alias and trade name have also been noticed by us.
    The way of observing chemistry, there are many people who have the same thing but different names. This 3 - Bromo - 4 - Fluoroiodobenzene, or another name, is used in different situations and uses. The establishment of trade names is related to the circulation and identification of the market.
    When we explore, we are well aware of the complexity of its synonyms. Only by recognizing its name can we be correct and smooth in research and application. This is not only related to academic rigor, but also to the operation of the industry. Therefore, it is an important task for chemical research to study its synonymous names and trade names in detail. In future explorations, we should also maintain a cautious heart and study the various names of this thing in order to achieve the wonders of chemistry.
    Safety & Operational Standards
    3 - Bromo - 4 - Fluoroiodobenzene - Safety and Operating Specifications
    Fu 3 - Bromo - 4 - Fluoroiodobenzene is an important item in chemical research. During its experimental operation and use, safety is a must and should not be ignored.
    First words Storage. This compound should be kept in a cool, dry and well-ventilated place. Avoid open flames and hot topics to prevent accidents. It must be isolated from oxidants, active metals, etc., to avoid chemical reactions. The container should also be well sealed to prevent leakage.
    As for the operation, the experimenter must wear appropriate protective equipment. Such as protective glasses, which can protect the eyes and avoid splashing liquid injury; gas masks, which can block the inhalation of harmful gases; protective gloves to prevent contact with the skin. There should be good ventilation equipment in the operation room, so that the volatile gas can be discharged in time.
    If a leak unfortunately occurs, evacuate the personnel first and isolate the scene. Emergency responders must take professional protection to prevent the spread of leaks. Small leaks can be absorbed by inert materials such as sand and vermiculite; large leaks need to be built embankments or dug for containment, and then properly disposed of.
    Furthermore, after use, the remaining items should not be discarded at will. When sent to a special treatment facility according to the prescribed method. The experimental equipment should also be thoroughly cleaned, except for the residual 3 - Bromo - 4 - Fluoroiodobenzene, to prevent contamination of the follow-up experiment.
    In short, the whole use of 3 - Bromo - 4 - Fluoroiodobenzene should strictly abide by safety and operating standards to ensure the smooth experiment, personnel safety and environment.
    Application Area
    3 - Bromo - 4 - Fluoroiodobenzene is also a chemical substance. Its use is good, and it can be used in the field of chemical research. Based on this, it can be synthesized with a variety of special effects, or can be used to treat specific diseases.
    And in the context of materials science, it can be used to improve the performance of high-performance materials. Make the material have special physical and chemical properties, such as increasing performance, qualitative quality, etc., and use it in sub-devices and optical devices to help improve its performance.
    Furthermore, it is an important starting material for synthesis. Due to its special characteristics, it is essential to improve the performance of various compounds, to develop the properties of chemical compounds, and to promote the development of chemical families, which is of great significance in a wide range of fields.
    Research & Development
    Recently, in my laboratory, I focused on studying a compound called 3-Bromo-4-Fluoroiodobenzene. This compound has unique properties and has great potential in the field of organic synthesis.
    I initially investigated its chemical structure in detail to clarify its reactive activity check point. After many theoretical deductions and simulation calculations, the surrounding area of bromine, fluorine and iodine atoms was locked as the key reaction area.
    Then a series of experimental investigations were carried out. A variety of classical organic reaction pathways were used to try to derive and modify it. In terms of reaction conditions, the type and dosage of temperature, solvent and catalyst were carefully regulated. After repeated trial and error, a set of better reaction parameters was gradually obtained, and the target derivatives could be obtained in higher yields.
    Looking to the future, it will further expand its application in the field of drug synthesis and materials science. It is hoped that through the continuous research and development of 3 - Bromo - 4 - Fluoroiodobenzene, it will contribute to the progress of related fields and promote this compound from laboratory research to a new stage of practical application, and realize its greater value.
    Toxicity Research
    Yu Taste is dedicated to the exploration of chemical properties, and recently focused on the toxicity study of 3-Bromo-4-Fluoroiodobenzene.
    At first, the molecular structure of the compound was observed, and the atoms of bromine, fluorine and iodine were attached to the benzene ring. This structure may cause it to have special chemical activities, and the activity is often related to toxicity.
    Then it was measured by various experiments. In cell experiments, its effects on cell growth and metabolism were observed. It can inhibit cell proliferation, and the higher the concentration, the more obvious the inhibition. Animals were also tested to observe their reactions after oral and percutaneous poisoning. Animals showed a slow movement, reduced eating, and pathological changes in their organs.
    In conclusion, 3 - Bromo - 4 - Fluoroiodobenzene is obviously toxic. The follow-up study of its toxicological mechanism should provide a basis for protection and treatment to prevent it from harming the environment and organisms.
    Future Prospects
    Wuguanfu 3 - Bromo - 4 - Fluoroiodobenzene This product has extraordinary potential and has great potential for future development. Its structure is unique, its properties are unique, and it may emerge in various fields.
    In the field of medicinal chemistry, it is expected to provide a key cornerstone for the development of new drugs. With its characteristics, it may be able to accurately act on lesions and bring good news to patients. In material science, it may also give birth to novel materials, endow them with unique properties, and apply them to high-end scientific and technological products.
    We should study diligently, explore its mysteries in depth, and tap its hidden value. We hope to make unremitting efforts to open up new frontiers, so that 3 - Bromo - 4 - Fluoroiodobenzene will shine in the future, for the well-being of the world, and a great cause for thousands of years. This is the future prospect of our generation.
    Where to Buy 3-Bromo-4-Fluoroiodobenzene in China?
    As a trusted 3-Bromo-4-Fluoroiodobenzene 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 3-Bromo-4-Fluoroiodobenzene 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 3-Bromo-4-Fluoroiodobenzene?
    3-Bromo-4-fluoroiodobenzene is also an important intermediate in organic synthesis. It has a wide range of uses in the field of medicinal chemistry. When synthesizing medicine, it is often necessary to introduce specific functional groups to create molecules with specific biological activities. 3-Bromo-4-fluoroiodobenzene contains functional groups of bromine, fluorine and iodine. These functional groups are active and can take advantage of various organic reactions such as nucleophilic substitution and coupling reactions to interact with other reagents, thus forming complex pharmaceutical intermediates, which pave the way for the creation of new drugs.
    In the field of materials science, it also has extraordinary performance. When synthesizing materials, it is necessary to accurately construct molecular structures in order to give materials special optoelectronic, electrical and other properties. The functional groups of 3-bromo-4-fluoroiodobenzene can participate in complex reactions to synthesize organic materials with specific structures, such as organic semiconductor materials. By participating in the reaction, the conjugate structure of the material molecules can be regulated, which has a significant impact on the photoelectric properties of the material. It can be used in the preparation of organic Light Emitting Diodes, field effect transistors and other devices.
    In addition, in the field of pesticide chemistry, it is also a key synthetic raw material. Pesticide creation requires active ingredients with unique structures. With its functional group reactivity, 3-bromo-4-fluoroiodobenzene can be converted into pesticide active intermediates with insecticidal, bactericidal, herbicidal and other effects. After subsequent reaction steps, various high-efficiency and low-toxicity pesticides are made to escort agricultural production. In short, 3-bromo-4-fluoroiodobenzene has an indispensable position in many chemical-related fields, promoting technological innovation and development in various fields.
    What are the physical properties of 3-Bromo-4-Fluoroiodobenzene?
    3-Bromo-4-fluoroiodobenzene is an important compound in organic chemistry. Its physical properties are quite worthy of investigation.
    First of all, its appearance is usually a colorless to light yellow liquid. At room temperature and pressure, it has a certain fluidity and a relatively uniform state. Its light color is due to the interaction of atoms in the molecular structure, and no groups with dark color are formed due to significant absorption of visible light bands.
    times and its boiling point. The boiling point of this compound is related to the intermolecular force. There is a van der Waals force between molecules, and the existence of halogen atoms such as bromine, fluorine, and iodine makes the molecules have a certain polarity and enhances the intermolecular force. Therefore, its boiling point is relatively high, about a specific temperature range. This temperature is the embodiment of the energy required to ensure that the molecule overcomes the intermolecular forces and converts from liquid to gaseous.
    In addition, the melting point is also affected by the regularity of molecular arrangement and intermolecular forces. The molecular structure of 3-bromo-4-fluoroiodobenzene causes it to have certain characteristics in the solid state, and the melting point is within a certain range. At this temperature, the lattice structure begins to disintegrate, and the substance gradually changes from solid to liquid.
    In terms of solubility, because it is an organic compound and has a certain polarity, it has good solubility in common organic solvents such as dichloromethane, chloroform, and ether. This is based on the principle of similar phase dissolution. The molecules of organic solvents and 3-bromo-4-fluoroiodobenzene molecules can form appropriate interactions, so that they can be uniformly mixed. In water, due to the weak force between the molecules and water, and the molecular polarity is not enough to overcome the hydrogen bond network of water, the solubility is not good.
    In terms of density, due to the relatively large atomic masses of bromine, fluorine, iodine and other atoms in the molecule, the density of the compound is greater than that of common organic solvents, and it is also greater than that of water. In liquid mixed systems, it is often in the lower layer.
    In summary, the physical properties of 3-bromo-4-fluoroiodobenzene are closely related to its unique molecular structure. These properties are of great significance in many fields such as organic synthesis and chemical analysis, laying the foundation for its application.
    3-Bromo-4-Fluoroiodobenzene chemical synthesis methods
    The method of preparing 3-bromo-4-fluoroiodobenzene is mostly derived from the ingenuity of organic synthesis. Benzene compounds containing fluorine and bromine are often used as starting materials and converted into target products through multiple steps.
    One method can start with 4-fluorobromobenzene. Under appropriate reaction conditions, the iodine substitution reagent is used to interact with it. For example, the iodine element ($I_2 $) is selected and accompanied by a suitable catalyst and oxidant. Common oxidants such as cerium ammonium nitrate (CAN) can electrophilically replace specific positions of the benzene ring with iodine-assisted elements in a mild reaction environment. In 4-fluorobromobenzene, the localization effect of bromine and fluorine changes the electron cloud density at a specific position in the benzene ring, which is conducive to the attack of iodine atoms, and then iodine atoms are introduced into the specific part of the benzene ring, and finally 3-bromo-4-fluoroiodobenzene is obtained.
    Furthermore, 3-bromo-4-fluoroiodoaniline can also be used as raw material. First, it is diazotized, and sodium nitrite and an appropriate amount of inorganic acid (such as hydrochloric acid) are used at low temperature to form diazonium salts. Then the diazonium salt reacts with iodine sources such as potassium iodide, and the diazonium group is replaced This process requires precise temperature control to maintain the stability of diazonium salts and prevent side reactions from occurring.
    Another way is to introduce bromine, fluorine and iodine atoms through halogenation reaction based on benzene derivatives containing suitable substituents. If bromine atoms are introduced first, the electron cloud distribution of the benzene ring is adjusted by specific reaction conditions, then fluorine atoms are introduced, and finally iodine atoms are introduced, then this path requires high control of reaction conditions and selectivity of each step of the reaction. Each method needs to consider the availability of raw materials, the difficulty of reaction, the yield and the number of side reactions, and weigh and choose the best way to synthesize 3-bromo-4-fluoroiodobenzene.
    3-Bromo-4-Fluoroiodobenzene What are the precautions in storage and transportation?
    3-Bromo-4-fluoroiodobenzene is an organic compound. When storing and transporting, many matters need to be paid attention to.
    When storing, choose the first environment. It should be placed in a cool, dry and well ventilated place, and must not be exposed to high temperature and humid environment. Due to its active nature, high temperature is easy to decompose, and moisture will also cause it to react with moisture, which will affect the quality. Furthermore, it needs to be kept away from fire, heat and oxidants. This compound is flammable, and there is a risk of combustion and explosion in case of open flame, hot topic or oxidant.
    Packaging is also crucial. Be sure to choose suitable packaging materials to ensure sealing and prevent leakage. It is usually packed in glass bottles or special plastic bottles, and the stopper needs to be tightly sealed.
    When transporting, relevant regulations and standards must be followed. Transportation vehicles should be equipped with corresponding fire equipment and leakage emergency treatment equipment to prevent accidents. During loading and unloading, operators need to handle it with care to avoid collisions and falls, so as to prevent material leakage caused by package damage.
    Once a leak occurs, personnel should be quickly evacuated to a safe area, and irrelevant personnel should be strictly prohibited from approaching. Emergency responders need to wear protective equipment and take corresponding measures according to the amount of leakage and the situation of the site. A small amount of leakage can be absorbed by inert materials such as sand and vermiculite; if a large amount of leakage, it needs to be built into a dike or dug for containment, and then properly handled.
    In conclusion, the storage and transportation of 3-bromo-4-fluoroiodobenzene must be carried out with care and follow strict operating procedures to ensure the safety of personnel and the environment from contamination.
    3-Bromo-4-Fluoroiodobenzene impact on the environment and human health
    3-Bromo-4-fluoroiodobenzene is a genus of organic compounds. Its impact on the environment and human health is of great concern to the world.
    At the environmental end, if this compound is released in nature, its chemical structure is stable, degradation is quite difficult, or it may remain in soil and water bodies for a long time. In soil, it may affect soil quality, interfere with the uptake of nutrients by plant roots, and then affect plant growth and development, causing changes in the type and quantity of vegetation, and disrupting ecological balance. In water bodies, it may harm aquatic organisms because of its bioaccumulation, transmission along the food chain, or toxic effects on high-trophic organisms, affecting the structure and function of aquatic ecosystems.
    As for personal health, 3-bromo-4-fluoroiodobenzene may be ingested into the human body through respiratory tract, skin contact and diet. It may be irritating. If it comes into contact with the skin, it can cause redness, swelling, itching, pain and other symptoms of the skin; if it enters the eyes, it will cause even more damage to the eyes, or cause congestion of the conjunctiva of the eye and visual impairment. Inhalation through the respiratory tract can irritate the mucosa of the respiratory tract, causing cough, asthma, breathing difficulties, etc. And this compound may be potentially toxic. After entering the human body, it may interfere with the normal physiological and biochemical processes of the human body, involve the function of important organs such as the liver and kidneys, and increase the risk of cancer for a long time.
    In conclusion, 3-bromo-4-fluoroiodobenzene poses a potential threat to both the environment and human health. When manufacturing, using, and disposing of this compound, it is necessary to exercise caution and take appropriate protective and disposal measures to reduce its harm to the environment and people.