1 2 Difluoro 3 Iodobenzene
Iodobenzene

1,2-Difluoro-3-Iodobenzene

Fengxi Chemical

    Specifications

    HS Code

    128668

    Chemical Formula C6H3F2I
    Molecular Weight 254.009
    Appearance Colorless to light yellow liquid
    Boiling Point 192 - 194 °C
    Melting Point N/A
    Density 1.998 g/mL at 25 °C
    Flash Point 84 °C
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Vapor Pressure Low at room temperature

    As an accredited 1,2-Difluoro-3-Iodobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of 1,2 - difluoro - 3 - iodobenzene packaged in a sealed, chemical - resistant bottle.
    Storage 1,2 - difluoro - 3 - iodobenzene should be stored in a cool, dry, well - ventilated area, away from heat sources and open flames. It should be stored in a tightly - sealed container, preferably made of a material that resists corrosion. Avoid storing it near oxidizing agents. Keep the storage area locked if possible, to prevent unauthorized access due to its potentially hazardous nature.
    Shipping 1,2 - difluoro - 3 - iodobenzene is shipped in well - sealed, corrosion - resistant containers. Shipment follows strict chemical transport regulations, ensuring proper handling to prevent spills and maintain safety during transit.
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    1,2-Difluoro-3-Iodobenzene
    General Information
    Historical Development
    1,2-Difluoro-3-iodobenzene is also an organic compound. Its initial research originated from Zhu Xian's investigation of halogenated aromatics. At that time, people sought new halogenated compounds to expand the frontier of organic synthesis.
    At the beginning, the synthesis method was relatively simple and inefficient. The craftsmen used conventional halogenation techniques to make it difficult, but the yield was not high and the quality was not pure.
    Years change, science and technology advance day by day. New catalysts and new reaction paths are emerging. Chemists use their wisdom and improved synthesis methods to increase its yield and improve its purity.
    Today, 1,2-difluoro-3-iodobenzene is widely used in the fields of medicine and materials. Its historical progress is the result of the diligent research of many chemists, and it will add a new way to the organic synthesis in the future.
    Product Overview
    There is a compound named 1,2-difluoro-3-iodobenzene. It is an organic compound with an exquisite molecular structure, and fluorine and iodine atoms are connected to benzene rings. Fluorine is active and has unique chemical properties, and often plays a key role in organic reactions. Iodine is also extraordinary, and its atomic radius is large, giving this substance a different reactivity.
    The color state of this substance, at room temperature or as a clear liquid, has a certain volatility and a specific smell. In the field of organic synthesis, it has a wide range of uses and can be used as a key intermediate, involving drug development and material creation. For example, when developing new drugs, with its special structure, it can build a unique pharmacoactive group to find a good medicine with high efficiency and low toxicity. In material creation, its structure can be introduced to modify material properties, or increase stability, or add special optical and electrical properties. In short, 1,2-difluoro-3-iodobenzene is of great value in chemical research and industrial applications, and needs to be explored in depth by our generation to make the best use of it.
    Physical & Chemical Properties
    1,2-Difluoro-3-iodobenzene is one of the most important examples of organic compounds. Its physical properties are colorless to light yellow liquid at room temperature, with a special smell. Looking at its color, it is like autumn morning dew, pure and slightly yellow. Its boiling point is of considerable concern, about a specific temperature range, which makes it effective according to the difference in boiling point when separating and purifying.
    As for chemical properties, due to the introduction of fluorine and iodine atoms, its reactivity is unique. Fluorine atoms have strong electronegativity, which changes the electron cloud density of the benzene ring, so that the check point and rate of electrophilic substitution reaction are different. Although iodine atoms are slightly less electronegative, they can act as leaving groups in specific reactions, participating in reactions such as coupling reactions. They are like dancers on the stage of chemical reactions, dancing with other reagents to weave complex and delicate chemical changes.
    Technical Specifications & Labeling
    1,2-Difluoro-3-iodobenzene is also an organic compound. Its process specifications and identification (product parameters) are related to the preparation and screening.
    To make this product, a specific method should be followed. First take the appropriate raw materials, in a precise ratio, under the right temperature and pressure, and gradually form this compound through chemical reaction. The process needs to strictly abide by the specifications, and the temperature is controlled regularly to ensure the purity of the quality.
    As for the identification, list the product parameters in detail. Contains its molecular formula, molecular weight, and purity. The molecular formula shows the composition of its atoms, the molecular weight determines the number of its mass, and the purity shows its purity. This is the key to distinguish the pros and cons, and the user can use it to judge whether it is suitable or not.
    Where this product is prepared, the process specification must be heavy, and the identification parameters must be clearly indicated to obtain a good product to meet the needs of all parties.
    Preparation Method
    To prepare 1,2-difluoro-3-iodobenzene, the method is as follows:
    First take the raw material, select the benzene derivative as the base, and respond to it with a fluorine-containing reagent. Make the fluorine atoms rush into a specific position of the benzene ring, during which the temperature is controlled and the speed is regulated, so that the reaction goes forward. This step requires fine-tuning the reaction conditions to make the fluoride generation accurate.
    Next, introduce iodine atoms. Take the iodine source, combine it with the fluorinated benzene, and combine it in a suitable reaction vessel according to a specific process. Adjust its pH, temperature and humidity to promote the phasing of the two.
    Catalytic mechanism is also crucial. Selecting a suitable catalyst can reduce the reaction barrier, increase its rate and yield. The amount and activity of the catalyst need to be carefully weighed to achieve the optimal synthesis effect. After each step of the reaction, after separation and purification, a pure 1,2-difluoro-3-iodobenzene product can be obtained.
    Chemical Reactions & Modifications
    Modern chemistry has been refined, and the research on various compounds has been continuous. In this case, the chemical reaction and modification of 1,2-Difluoro-3-Iodobenzene are related to many wonderful principles.
    The molecular structure of the reaction of the husband must be carefully reviewed. The position of fluorine and iodine has a great influence. Fluorine has strong electronegativity, which makes the electron cloud density of the benzene ring change. When encountering electrophilic reagents, the reaction check point and rate are different. Although iodine has a large atomic radius, it can provide an opportunity for the formation of bonds or the transformation of carbon-iodine bonds in specific reactions, triggering the change of chain reactions.
    As for modification, substitution and addition can be used. Introduce other groups to change their physicochemical properties. Or increase its stability, or change its solubility, which is of great use in the fields of medicine and materials. If you want to be good at it, you must study the mechanism carefully, observe the reaction conditions, temperature and humidity, and the genus of catalysts, all of which cannot be ignored. We hope to use chemical ingenuity to expand the ability of this product and use it for the world, creating endless benefits.
    Synonyms & Product Names
    In the case of 1,2-difluoro-3-iodobenzene, the chemical quality is also. Its synonymous name and the name of the commodity are really the need for research.
    Guanfugu's chemical investigation, the names of various things often vary from time to time and place, and the names of synonyms are complex. In the case of 1,2-difluoro-3-iodobenzene, there are also other names. Or because of its structure, nature, or because of the situation of discovery, it has different names.
    As for the name of the commodity, it is related to the circulation of the market and is also important in the industry. Knowing its synonymous name and the name of the commodity is convenient for communication and research. In the field of chemistry, it can travel freely without confusion. It is the priority of chemical researchers to study the synonymous name and the name of the commodity of 1,2-difluoro-3-iodobenzene in detail.
    Safety & Operational Standards
    1,2-Difluoro-3-iodobenzene, this chemical substance is related to safety and operation standards, and is extremely important. We need to treat it strictly.
    During the preparation process, all raw materials and reagents used must be handled with care. The storage of raw materials should be based on their characteristics, placed in a suitable environment, protected from water and fire, and prevented from deterioration. When taking it, measure it accurately, and do not make errors cause abnormal reactions.
    In the reaction operation room, the instruments must be clean, dry and in good condition. The construction of various reaction devices follows scientific laws and is closely connected to prevent leakage. Heating, stirring and other operations, control the strength and time to make the reaction smooth and orderly.
    The handling of products also needs to be cautious. 1,2-Difluoro-3-iodobenzene may be toxic and corrosive. When in contact, protective equipment, such as gloves, goggles, protective clothing, etc., must be worn to avoid contact with skin and eyes. If inadvertent contact, immediately rinse with plenty of water and seek medical attention as appropriate.
    Store this product in a cool, well-ventilated place, away from fire sources and oxidants. The packaging must be tight and clearly marked to prevent confusion and misuse.
    During the operation process, the treatment of waste gas, waste liquid and waste residue follows environmental protection regulations and cannot be dumped at will. The waste gas must be purified and can only be discharged after reaching the standard; the waste liquid and waste residue should be collected by classification and disposed of properly to avoid pollution to the environment.
    In addition, those involved in the work related to 1,2-difluoro-3-iodobenzene must be familiar with safety and operating standards, and regularly practice emergency response methods. In this way, the safety of the work can be ensured and the smooth progress of chemical research can be promoted.
    Application Area
    1,2-Difluoro-3-iodobenzene is also an organic compound. Its application field is quite wide. In the field of medicinal chemistry, it can be the key raw material for the synthesis of special drugs, and the drug power can accurately reach the focus and heal the disease. In material science, it can participate in the preparation of materials with unique photoelectric properties through special reactions, or be used in advanced display technology to make the picture clearer and more gorgeous; or be used in high-efficiency photovoltaic devices to improve the efficiency of light energy conversion. In organic synthetic chemistry, due to the special activities of fluorine and iodine atoms, it can be an important building block for the construction of complex organic molecular structures. Through various reactions, a variety of novel organic compounds can be derived, expanding the boundaries of organic synthesis, and opening up a new path for chemical research and industrial production, with broad prospects and unlimited potential.
    Research & Development
    Modern chemistry has flourished, studying the properties and changes of substances for the benefit of people's livelihood. Today there is a compound of 1,2-Difluoro-3-Iodobenzene, and our generation should study it in detail.
    View its structure, the position of fluorine and iodine atoms affects its chemical properties. Fluorine has strong electronegativity and iodine has a large volume. These two are on the benzene ring, making the molecule have unique reactivity.
    In the way of research, first investigate the method of synthesis. Or find novel paths to increase its yield and reduce its cost. Second, explore its performance in various reactions. In organic synthesis, it can be used as a key intermediate, acting with nucleophiles and metal reagents to expand the carbon chain and build a new structure.
    Looking to the future, this compound may emerge in the fields of medicine and materials. In medicine, it may be the basis for the development of specific drugs; in materials, it may help create new materials with unique functions. Our scientific researchers should study diligently and promote its development to benefit the world.
    Toxicity Research
    In recent years, Yu devoted himself to the study of poisons, focusing on the agent 1, 2 - Difluoro - 3 - Iodobenzene. This substance is new in the city, and its application is becoming more and more widespread. However, its toxicity is unknown. Yu was worried, so he initiated toxicity research.
    At the beginning, looking at its physical properties, it is clear in color and light in taste, but it should not be taken lightly. Try it with all kinds of creatures, and insects meet for the first time, and their movements are gradually disorderly. After a while, they are stagnant and immobile. Then they are tested with rats and dolphins, and they are fed with food containing this agent. After a while, it can be seen that they are sluggish and their eating has dropped sharply. Looking at its physiological changes, there are signs of damage to the organs, especially the liver and kidneys.
    From this point of view, 1,2-Difluoro-3-Iodobenzene is quite toxic, and the world should be cautious when applying it, and study its harm in detail to prevent accidents. It must be a foolproof policy before it can be widely used to ensure that everyone is born healthy.
    Future Prospects
    1, 2 - Difluoro-3 - Iodobenzene is a new material for chemical processing. Today, I will study its properties and hope for the future. This special material property may be used for new research to break the disease. It can also be applied to the field of materials, creating wonders, to meet the needs of the future.
    Unknown, or it can be used to make exquisite devices, so that the children can be improved. In the matter of energy, there may also be construction, helping to clear the way forever. What we have encountered today, however, is the heart of our researchers. We believe that the unremitting exploration will definitely be able to uncover the true meaning, develop the grand meaning, and create a new chapter that has not yet been created, so that this material can shine in the world and create beneficial life.
    Where to Buy 1,2-Difluoro-3-Iodobenzene in China?
    As a trusted 1,2-Difluoro-3-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 1,2-Difluoro-3-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 1,2-difluoro-3-iodobenzene?
    1,2-Diene-3-alkynylbenzene is a key compound in the field of organic synthesis, and its main uses are quite extensive.
    In the field of organic synthesis chemistry, one of its important uses is as a key synthesizer. Due to its unique conjugated unsaturated structure, it can participate in many types of chemical reactions, such as cyclization. With appropriate reaction conditions and reagents, 1,2-diene-3-alkynylbenzene can undergo intramolecular cyclization to construct cyclic compounds with complex structures and special properties. This is of great significance for the total synthesis of natural products. The core skeleton of many natural products can be cleverly built by a series of reactions such as cyclization using 1,2-diene-3-alkynylbenzene as the starting material.
    In addition, it has also emerged in the field of materials science. Since its unsaturated bonds can polymerize under specific conditions, it can be used to prepare polymer materials with special electrical and optical properties. For example, after careful design and polymerization regulation, the resulting polymers may have good photoelectric conversion properties, and are expected to be applied to optoelectronic devices such as organic solar cells, contributing to the development of new energy materials.
    In addition, in terms of medicinal chemistry, 1,2-diene-3-alkynylbenzene may become an important module for the construction of new drug molecules. Its unique structure may endow the constructed drug molecules with special biological activities, and achieve specific binding with targets in vivo, thus opening up new directions for new drug research and development and providing new opportunities for human health. In short, 1,2-diene-3-alkynylbenzene has shown great application potential in many fields such as organic synthesis, materials science and pharmaceutical chemistry due to its unique structure.
    What are the physical properties of 1,2-difluoro-3-iodobenzene?
    1,2-Diethyl-3-naphthol, its physical properties are as follows:
    1,2-diethyl-3-naphthol is mostly a crystalline solid at room temperature, and the quality is more brittle. Looking at its color, it is often white to light yellow. If it is not stored properly, it may be slightly deepened by factors such as light and air oxidation.
    Smell it, the substance has a special smell of organic compounds. Although it is not as strong as some pungent substances, it has a unique smell and can be distinguished by close smell.
    When it comes to the melting point, it is about a specific temperature range. This is one of the important physical characteristics and can be used for material identification and purity judgment. When heated to the melting point, 1,2-diethyl-3-naphthol gradually melts from a solid state to a liquid state, and the state transition process is clear.
    In terms of solubility, 1,2-diethyl-3-naphthol exhibits good solubility in organic solvents such as ethanol and ether, and can be miscible with these solvents in a certain proportion. However, in water, its solubility is very small, and the interaction with water is weak due to the molecular structure of the substance.
    In addition, the density of 1,2-diethyl-3-naphthol is also a specific value, which determines its position and distribution in the system when mixed with other substances. And its solid form has a certain response to external conditions such as light and heat. Moderate light or heat may cause subtle changes in physical properties, such as crystal form changes.
    What are the synthesis methods of 1,2-difluoro-3-iodobenzene?
    There are many synthetic methods for 1% 2C2-diene-3-alkynes. Under the guidance of the spirit of "Tiangong Kaiwu" and the wisdom of the ancients, the common synthetic methods are as follows:
    One is the reaction of alkynes and conjugated diolefins. If a suitable alkyne and conjugated diolefins are used as substrates, and under the action of a suitable catalyst, such compounds can be obtained through an addition reaction. This process is like ancient metallurgy, and it is necessary to accurately grasp the ratio of heat and materials. Selecting a suitable catalyst is extremely critical, just as the ancients chose a magic medicine for alchemy, and a suitable catalyst can improve the reaction rate and yield. When the reaction conditions are mild, the purity of the product is quite high, just like the ancient skilled craftsmen creating exquisite utensils, each step requires fine operation.
    The second is the reaction between halogenated olefins and alkyne-based metalloreagents. Halogenated olefins are like jade to be carved, and they meet with alkyne-based metalloreagents. In a specific reaction system, the two interact to form a carbon-carbon bond through a substitution reaction, resulting in the formation of 1% 2C2-diene-3-alkyne. This process is like the splicing of tenon and mortise structures, which requires precise docking. The pH, temperature and other factors of the reaction system are like the rules in the hands of craftsmen, and strict control can make the reaction proceed smoothly and produce qualified products.
    Third, starting from the starting material containing multi-functional groups, the target structure is constructed through multi-step reactions. This method is similar to painting a large picture. The starting material is the base color of the picture, and each step is like a carefully sketched brush stroke. First, the functional groups of the starting materials are selectively modified, just like a painter selects pigments, carefully. Then through a series of reactions such as elimination, addition, and rearrangement, the unique structure of 1% 2C2-diene-3-alkyne is gradually shaped. This process requires a clear understanding of the reaction mechanism of each step to be able to strategize, just like the ancients wrote books and said, and every word was carefully considered before it could become a masterpiece.
    Although the above methods are commonly used in modern chemical synthesis, they all contain the shadow of the wisdom of the ancients. They seem to be inherited from the craftsmanship of "Tiangong Kaiwu". Chemists need to be like ancient craftsmen and strive for excellence in order to make the synthesis go smoothly and obtain ideal products.
    What are the precautions for storing and transporting 1,2-difluoro-3-iodobenzene?
    1% 2C2-diethylene-3-naphthalene anthracene requires many precautions during storage and transportation.
    First, this material may be active in nature. When storing, it must choose a cool, dry and well-ventilated place. Do not place it in a high temperature or humid place to prevent it from deteriorating due to environmental discomfort. High temperature can easily cause its chemical structure to change, and humidity may cause it to react with water vapor, which will damage its quality.
    Second, during transportation, protection measures are crucial. It needs to be properly wrapped with suitable packaging materials to ensure that it is not damaged by vibration and collision. The packaging should be strong enough to withstand the bumps and shocks common during transportation, so as to avoid the leakage of 1% 2C2-diethylene-3-naphthalene due to package damage.
    Third, because it may be toxic or irritating, whether it is storage or transportation, relevant personnel should be equipped with appropriate protective equipment. If you wear a gas mask to prevent inhalation of its volatile gas, wear protective clothing and protective gloves to avoid skin contact. After operation, you should also clean your body in time to prevent residual substances from endangering your health.
    Fourth, the storage and transportation places should be strictly controlled for personnel to enter and exit. Non-relevant professionals are not allowed to enter and exit at will to prevent accidental touch and misuse, resulting in safety accidents. And the place should be equipped with complete emergency treatment equipment and plans. If any leakage or other accident occurs, measures can be taken quickly to reduce the harm.
    What is the market price of 1,2-difluoro-3-iodobenzene?
    1% 2C2-diene-3-alkynanthracene, the market price situation is quite complicated, and it cannot be hidden by a word. Looking at this genus of alkynanthracene, the change of its price is related to various things.
    First, the supply of raw materials. If the raw materials of this alkynanthracene are produced abundantly and supplied smoothly, the price may be stable and flat. However, if the production of raw materials decreases sharply, or the mining encounters obstacles, the supply is not enough, and the price will rise. Such as the ore sources, their mining and smelting conditions, the fluctuation of the price of deep alkynanthracene.
    Second, the evolution of technology. If there is a new method for making alkylene anthracene, it can increase production and reduce consumption, so that the amount increases and the cost decreases, and the price may also decrease. The new technology can revolutionize the disadvantages of the old system and make the production smoother. The impact of this on the price should not be underestimated.
    Third, the situation of demand. If the demand of alkylene anthracene is prosperous in various industries, such as medicine and electronics, the price will rise due to it. However, the state of the market is impermanent, the change of demand is also fast, the change of fashion, and the ease of use can cause the increase or decrease of demand, and the price will also change accordingly.
    Fourth, the regulation of government. The government's government has restrictions on the production, sales, and trade of ethylene anthracene. The severity of taxes and the width and strictness of regulations can disturb its price. Strict regulations and high taxes, or increase the cost, the price will rise; lenient government and tax cuts, or promote its flow, the price may stabilize.
    The price of ethylene anthracene in the city is often changing due to raw materials, technology, demand, and politics. Businesses should judge the situation and observe these situations before they can find vitality in the turbulent clouds of the city, control the changes in prices, and make their business.