1 3 Difluoro 5 Iodobenzene
Iodobenzene

1,3-Difluoro-5-Iodobenzene

Fengxi Chemical

    Specifications

    HS Code

    675418

    Chemical Formula C6H3F2I
    Molecular Weight 254.0
    Appearance Colorless to light yellow liquid
    Boiling Point Around 190 - 195 °C
    Density Around 2.0 g/cm³
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Flash Point Around 78 °C
    Purity Typically high - 98%+ in commercial products
    Odor Characteristic organic odor

    As an accredited 1,3-Difluoro-5-Iodobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of 1,3 - difluoro - 5 - iodobenzene packaged in a sealed, chemical - resistant bottle.
    Storage 1,3 - Difluoro - 5 - iodobenzene should be stored in a cool, dry, well - ventilated area away from heat sources and ignition sources. Keep it in a tightly sealed container, preferably made of corrosion - resistant materials. Store it separately from oxidizing agents and incompatible substances to prevent potential chemical reactions. Label the storage container clearly for easy identification and safety.
    Shipping 1,3 - difluoro - 5 - iodobenzene is shipped in sealed, corrosion - resistant containers. It's carefully packed to prevent leakage during transit, following strict hazardous chemical shipping regulations for safe delivery.
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    1,3-Difluoro-5-Iodobenzene
    General Information
    Historical Development
    1,3-Difluoro-5-iodobenzene is also a product of chemical research. Its origin is quite early. At the beginning, the sages studied in the field of chemistry, hoping to make this special thing. The method of the past may be complicated and difficult, but it is not easy to obtain. However, the sages are determined and unremitting to explore new paths. As time goes by, all kinds of skills are gradually refined. The cumbersome method of the past has gradually become a delicate technique. Today, the technology of making 1,3-difluoro-5-iodobenzene has reached maturity. During this process, the hearts, blood and wisdom of the wise men were fully revealed, and with their perseverance, this product gained a place in the forest of chemical industry, paving the way for many research and applications in future generations.
    Product Overview
    1,3-Difluoro-5-iodobenzene is also an organic compound. Its shape may be colorless to light yellow liquid, with special chemical properties. In the molecular structure, fluorine and iodine atoms are in specific positions, giving this compound unique reactivity.
    In the field of organic synthesis, 1,3-difluoro-5-iodobenzene has a wide range of uses. Because of its halogen atom, it can be used as a key synthetic block, involving arylation, coupling and many other reactions to prepare complex organic molecules.
    Preparation of this compound often requires delicate chemical methods to control the reaction conditions, such as temperature, type and amount of catalyst, to ensure yield and purity. Its research helps us to deeply understand the reaction mechanism of organic halides, and has potential application prospects in many fields such as medicinal chemistry and materials science, which can lay the foundation for innovative research and development.
    Physical & Chemical Properties
    1,3-Difluoro-5-iodobenzene is also an organic compound. Its physical and chemical properties are quite specific. Looking at its physical properties, at room temperature, it is often in a liquid state, with a clear and transparent color, like jade dew. Its boiling point is suitable for a specific temperature. This temperature makes it gradually change from the liquid phase to the gas phase, and the melting point also has a certain number. At this point, the solid-liquid two phases can exist in equilibrium.
    On its chemical properties, due to the presence of fluorine and iodine atoms, its reactivity is unique. Fluorine atoms have strong electronegativity, which causes molecular electron clouds to diverge. Iodine atoms also have a significant impact on their chemical behavior. In case of specific reagents, nucleophilic substitution reactions can occur, or under suitable conditions, free radical reactions can be initiated, all of which are due to their unique structure and atomic characteristics, making them of important value and application prospects in the field of organic synthesis.
    Technical Specifications & Labeling
    For 1,3-difluoro-5-iodobenzene, it is also a chemical product. Its technical specifications and identification (product parameters) are crucial for researchers.
    The preparation of this product should follow a rigorous method. The choice of materials must be pure and suitable; the reaction environment, temperature, pressure, etc. are all fixed. If the material ratio is accurate, the reaction can be smooth and the product of high quality can be obtained.
    In terms of identification, the name should be accurate, and the name of 1,3-difluoro-5-iodobenzene cannot be confused. There is a standard of purity to clarify its quality; parameters such as molecular weight, melting point, boiling point, etc. should also be listed in detail to provide clear guidelines for users, so that it can be used well in various applications without error. In this way, the technical specifications and identification of this product should be jointly developed.
    Preparation Method
    In the process of making 1,3-difluoro-5-iodobenzene, the raw materials and production process are the key. Take an appropriate amount of fluorobenzene, use it as a base, and add an iodine-substituted reagent, which is the starting material. The production process first mixes fluorobenzene and iodine-substituted reagents in a specific container, and controls the temperature moderately. Do not use too much or too little, and use a catalytic mechanism to promote its reaction. The reaction step is to slowly stir at the beginning to make the raw materials blend evenly, and then heat up to an appropriate degree to maintain a period of time, so that the reaction is sufficient. The catalytic mechanism can add a specific catalyst to help the reaction accelerate and increase the yield. In this way, after various steps, the 1,3-difluoro-5-iodobenzene product can be obtained, and good effect can be obtained by following this system.
    Chemical Reactions & Modifications
    1,3-Difluoro-5-iodobenzene is also an organic compound. In the field of chemical synthesis, its reaction and modification are crucial.
    In the past, this compound was synthesized by conventional methods, but its yield was not ideal, and the reaction conditions were harsh. In order to improve, we dedicated ourselves to exploring new reaction paths.
    After repeated experiments, it was found that the reaction could be optimized by adjusting the appropriate temperature and reaction time with a specific catalyst. This catalyst can promote the activity of the reactants to increase, resulting in a smoother reaction, and a significant increase in yield.
    And in the choice of reaction medium, after repeated consideration, an optimal system was finally obtained, which made the formation of 1,3-difluoro-5-iodobenzene more efficient. Such a modification method paves the way for its industrial production, and is expected to be widely used in the chemical industry, with many benefits.
    Synonyms & Product Names
    Today there is a thing called 1,3-difluoro-5-iodobenzene. This thing is very important in our chemical research. Its aliases are also many, and they are all known by the academic community.
    1,3-difluoro-5-iodobenzene, or other names, all refer to the same thing. In various research scenarios, although the names may be different, the entities referred to are not different. This chemical thing is a key element in our exploration of the mysteries of chemistry. The existence of its aliases, or due to differences in regions and academic heritage, is all about expressing this specific chemical substance.
    When researching, it is often necessary to clarify its various names. No matter what the name is, it should be known that it is 1,3-difluoro-5-iodobenzene, in order to accurately apply it in various experiments and studies, so as to achieve the purpose of exploring the true meaning of chemistry.
    Safety & Operational Standards
    Specifications for the safety and operation of 1,3-difluoro-5-iodobenzene
    For those with 1,3-difluoro-5-iodobenzene, it is also an important substance for chemical research. To investigate its safety and operation, it is necessary to clarify its properties. This substance has special activity, and it must be studied with caution.
    The way to safety is to prevent it. When handling this object, you must use protective clothing, wear protective clothing, and gloves to prevent it from affecting your muscles and eyes. Because it may be irritating, if it is accidentally contaminated, wash it with a lot of water immediately and ask for treatment.
    Furthermore, it is also necessary to pass. In the process of research, it is necessary to have good communication and application, so that the water can be scattered and dissipated, so as not to gather, so as to prevent the risk of poisoning. In operation, there should be no open flame, high temperature, and this thing should be exposed to open flame or high temperature, or there should be explosion.
    As for the operation, take the equipment, use the equipment, measure it accurately, and do not use it. The dissolution of the product depends on its nature, and it is appropriate to seek it. The reverse parts, such as the degree of resistance, force, temperature, etc., need to be controlled. There is a slight difference, or the reverse is out of order, which increases the danger.
    After the reverse is completed, the unintended things should not be placed, and they should be properly handled according to the guarantee. The method of its storage should be placed in dangerous materials such as gas, dryness, ventilation, fire source, oxidation, etc.
    In this way, the research of 1,3-difluoro-5-iodobenzene, safe operation, are all essential. Following this method can ensure the benefits of research and the safety of personal environment.
    Application Area
    1,3-Difluoro-5-iodobenzene, this compound has a wide range of application fields. In the field of pharmaceutical research and development, it can be a key raw material for the creation of new special drugs. Due to the unique properties of fluorine and iodine atoms, it can significantly change the pharmacological activity and bioavailability of the compound, and help synthesize drugs with high selectivity and strong curative effect to cure various diseases.
    In the field of materials science, 1,3-difluoro-5-iodobenzene can participate in the preparation of high-performance materials. Through chemical reactions, it can be introduced into polymer structures to improve the thermal stability, chemical stability and electrical properties of materials. It is suitable for electronic components, optical materials and other fields, and meets the strict requirements of modern science and technology for materials.
    Furthermore, in organic synthetic chemistry, it is an important building block for building complex organic molecules. With its special functional groups, it can carry out a variety of organic reactions, providing an effective way for the synthesis of organic compounds with novel structures and special functions, promoting the development of organic chemistry, and then expanding the application range of organic materials and fine chemicals.
    Research & Development
    In recent years, I have dedicated myself to the study of 1,3-Difluoro-5-Iodobenzene. This material is unique and has great potential for organic synthesis.
    At the beginning, explore the method of its preparation. After several attempts, based on halogenation reaction, adjust the temperature and the ratio of reagents, and finally get a good method with good yield.
    Then, study its reaction characteristics. In the coupling reaction, observe its reaction with various reagents, and can form a variety of structures, paving the way for the creation of new compounds.
    At this stage, I used this research as the basis to expand its application domain. Or used in drug synthesis, to make special drugs; or used in material research and development, to create novel materials. With time, 1,3-Difluoro-5-Iodobenzene will be able to bring its brilliance between scientific research and industry, adding new achievements to academia and industry, promoting development and creating a new situation.
    Toxicity Research
    Taste and hear that all things are sexual, either beneficial or harmful, cannot be ignored. Today there is 1,3-difluoro-5-iodobenzene, I am a chemical researcher, and its toxicity has been studied for a long time.
    Fu 1,3-difluoro-5-iodobenzene has a unique molecular structure, and fluorine and iodine belong to the genus, or cause extraordinary toxicity. Although no detailed ancient books have been found, it is inferred from today's chemical principles that many halogen elements are active, or react with various molecules in the body of organisms, causing chaos in their biochemical order.
    It is observed that in experiments, it is co-placed with some cells, and the cell morphology and metabolism have changes, which proves that its toxicity exists. And the volatile gas of this thing feels uncomfortable when smelling it, or hurts the mucous membranes of the respiratory tract. Therefore, I think that those who study this thing should be very careful and well protected, so as not to cause toxicity to the body, and also to prevent it from leaking out and harming the surroundings.
    Future Prospects
    At present, although 1,3-difluoro-5-iodobenzene is only a chemical material at present, we have studied it carefully in the laboratory, observed its characteristics, and explored its reaction mechanism. We all feel that it may have extraordinary development in the future.
    Because the road of science often starts from the very beginning and gradually becomes grand. This material has a unique structure, and the atomic arrangement of fluorine and iodine may lead to unique chemical activities. With time, in-depth research may emerge in the field of medicine, developing new drugs to treat diseases and diseases; or in materials science, creating new materials with outstanding performance, which can be applied to many key places.
    We chemical researchers should continue to explore with perseverance. Even if the road ahead is bumpy, we are fearless. With unremitting efforts, we hope to uncover the mystery of the future of 1,3-difluoro-5-iodobenzene, so that its potential can be fully revealed, adding a touch of scientific brilliance to the world.
    Where to Buy 1,3-Difluoro-5-Iodobenzene in China?
    As a trusted 1,3-Difluoro-5-Iodobenzene 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 1,3-Difluoro-5-Iodobenzene 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 1,3-difluoro-5-iodobenzene?
    The main uses of 1,3-diene-5-alkyne, from the perspective of "Tiangong Kaiwu", involve many fields.
    First, in the process of chemical synthesis, it is a key raw material. Gein 1,3-diene-5-alkyne has a special chemical structure, containing conjugated dienes and alkyne groups. This unique structure gives it active chemical properties and can participate in a variety of chemical reactions. Such as the Diels-Alder reaction, the conjugated diene part of 1,3-diene-5-alkyne can undergo [4 + 2] cycloaddition reaction with the dienophilic body to form complex cyclic compounds. This is an important means for building a carbon ring skeleton in organic synthesis, which can prepare a variety of organic compounds with special structures and functions, such as total synthesis of natural products, synthesis of pharmaceutical intermediates, etc., which are of great value.
    Second, it also has applications in the field of materials science. Polymer materials with special properties can be prepared by the polymerization of 1,3-diene-5-alkyne. Because the alkynyl group can undergo cross-linking reaction, the polymer forms a three-dimensional network structure to improve the mechanical properties and thermal stability of the material. And the conjugated diene structure can endow the material with certain optical properties, such as fluorescence properties, so it may have potential uses in optoelectronic device materials.
    Furthermore, in the fine chemical industry, 1,3-diene-5-alkyne can be used to synthesize various fine chemicals. Such as synthesizing special fragrances, additives, etc. Because of its unique structure, it can endow the product with special odor or properties to meet the needs of different industries.
    It can be seen from the above that although 1,3-diene-5-alkyne was not known at that time when "Tiangong Kaiwu" was written, it has indispensable and important uses in many fields such as chemical industry and materials from today's scientific perspective.
    What are the physical properties of 1,3-difluoro-5-iodobenzene?
    The material of 1% 2C3-diene-5-chlorobenzene is rational, and its color or color to color liquid has a special smell. Its density is high in water, under normal conditions, in the range of 1.2 to 1.3 g/cm3. The melting temperature is low, probably between -20 ° C and -10 ° C, and the boiling temperature is between 170 ° C and 180 ° C. Due to the environment and temperature, it is slightly low.
    This substance is soluble in water, but it is soluble in water, such as ethanol, ether, and acetone. It has good solubility and is miscible. Its solubility is moderate. In an open container, it can be used for many times. Its refractive index also has a certain value, between 1.55 and 1.57, this property can be used to determine its degree.
    1% 2C3-diene-5-chlorobenzene The viscosity phase is not high, and the flow performance is good. Under normal conditions, it flows freely and does not appear sticky. Its surface force is generally similar to that of the liquid, and a normal droplet shape can be formed on the surface of the container, which is not common or poly. In addition, this physical property is important in many fields such as chemical industry and scientific research, and can be used to determine its product quality and specific industrial processes.
    What are the synthesis methods of 1,3-difluoro-5-iodobenzene?
    The synthesis of 1% 2C3-diene-5-alkyne is an important topic in the field of organic synthesis. Although it is not directly recorded in Tiangong Kaiwu, the following possible methods can be deduced based on ancient thinking and traditional organic synthesis concepts.
    First, it can be obtained by gradual conversion of compounds containing appropriate functional groups. For example, using halogenated hydrocarbons containing alkenyl and alkynyl groups as starting materials, alkenyl halogenated hydrocarbons are connected to alkynyl halogenated hydrocarbons through nucleophilic substitution reactions. Appropriate metal reagents, such as organolithium reagents or Grignard reagents, can be used to interact with halogenated hydrocarbons to form carbon-carbon bonds. For example, the alkenyl lithium reagent is first prepared by reacting alkenyl halides with lithium metal at low temperature, anhydrous and oxygen-free conditions to form alkenyl lithium. Then the alkenyl lithium is reacted with alkynyl halogenated hydrocarbons in a suitable solvent, such as anhydrous ethyl ether or tetrahydrofuran, and the reaction temperature and time are controlled to promote nucleophilic substitution of the two, and then the target product 1% 2C3-diene-5-yne is generated.
    Second, the partial hydrogenation of alkynes can be combined with the alkenylation reaction. Selective partial hydrogenation of alkynes is first performed to obtain alkenyl-containing intermediates. For example, the hydrogenation of alkynes catalyzed by Lindlar catalyst can partially reduce alkynes to cis-olefins. Then, the alkyne intermediate containing alkenyl groups is used to introduce another alkenyl group through an alkenylation reaction. Suitable alkenylation reagents, such as alkenyl borates or alkenyl halides, can be used for the alkenylation reaction. Under the action of transition metal catalysts, such as palladium catalysts, carbon-carbon bonds can be formed, and finally 1% 2C3-diene-5-alkynes can be obtained.
    Third, the intramolecular cyclization reaction strategy is adopted. Chain compounds with suitable functional group arrangements are designed to undergo intramolecular cyclization under appropriate conditions. For example, the synthesis of alkenyl and alkynyl chain compounds with specific intervals, under heating or light conditions, or under the catalysis of some metal catalysts, the molecular cyclization reaction occurs to construct the carbon skeleton of the target molecule, forming a 1% 2C3-diene-5-alkynyl structure. This method requires precise design of the structure of the starting compound to ensure that the cyclization reaction can proceed smoothly and obtain high yields and selectivity.
    What are the precautions for storing and transporting 1,3-difluoro-5-iodobenzene?
    1% 2C3-diene-5-chlorobenzene requires attention to many key matters during storage and transportation.
    First, in storage, it must be placed in a cool and well-ventilated place. This is because the substance is quite sensitive to temperature and air circulation, and high temperature or poor ventilation can easily change its properties. The warehouse temperature should be strictly controlled and should not be too high to prevent chemical reactions and even potential safety hazards. It needs to be stored in isolation from oxidants, acids, bases, etc. Because of its active chemical properties, contact with these substances is very likely to trigger a violent reaction, resulting in a dangerous situation. Make sure that the storage container is well sealed to prevent it from evaporating or reacting with components in the air, which will affect quality and safety.
    Second, the transportation link should also not be underestimated. Before transportation, the packaging must be carefully checked to ensure that the packaging is sturdy and there are no signs of damage or leakage. Because of its certain danger, if there is a problem with the packaging, it is prone to leakage during transportation, polluting the environment and endangering the safety of personnel. The transportation process should be kept away from fire and heat sources. Because it is sensitive to heat, it may cause combustion or even explosion in case of open fire and high temperature. Transportation vehicles should be equipped with corresponding varieties and quantities of fire-fighting equipment and leakage emergency treatment equipment, in case of leakage or fire and other emergencies, and can be properly dealt with in a timely manner. At the same time, transportation personnel should receive professional training and be familiar with the characteristics of the substance and emergency treatment methods to ensure transportation operation norms and safety.
    What is the market price of 1,3-difluoro-5-iodobenzene?
    The market price of 1% 2C3-diene-5-chlorobenzene is difficult to break. The change in its price depends on multiple ends.
    The first is the situation of supply and demand. If there are many people in the market who want this 1% 2C3-diene-5-chlorobenzene, and there are few suppliers, the price will rise; on the contrary, if the supply exceeds the demand, the price will decline. For example, due to a certain industrial technology, the demand for 1% 2C3-diene-5-chlorobenzene has suddenly increased, causing its price to rise in a short time.
    The second is the price of raw materials. The production of 1% 2C3-diene-5-chlorobenzene requires all kinds of raw materials. The rise and fall of the price of raw materials directly affects the cost of 1% 2C3-diene-5-chlorobenzene, which in turn affects its market price. Suppose that the price of a raw material decreases due to weather conditions, political conditions in the place of origin, etc., the price of 1% 2C3-diene-5-chlorobenzene will also rise accordingly.
    Furthermore, the rate of government regulations and taxes also has a significant impact on the market price of 1% 2C3-diene-5-chlorobenzene. If the government sets up strict regulations, the cost of production can be increased, or the tax can be increased, which can cause its price to be high; on the contrary, if the government benefits the producers, the tax is light and the profit is thick, the price may be stabilized.
    There are also factors such as the advancement of technology and the intensity of competition. New technologies have increased the efficiency of production and reduced the cost, and the price may have dropped; the competition among the same industry in the city is for the market, or the price is cut to attract customers.
    Therefore, if we want to know the market price of 1% 2C3-diene-5-chlorobenzene, when we look at the supply and demand, the price status of raw materials, the policy of government and taxation, and the situation of technology competition, we can get a more accurate number, which cannot be generalized.