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2-(Trifluoromethyl)-1-Iodo-4-Nitrobenzene

2-(Trifluoromethyl)-1-Iodo-4-Nitrobenzene

Hongda Chemical

    Specifications

    HS Code

    988642

    Chemical Formula C7H3F3INO2
    Molecular Weight 329.003 g/mol
    Appearance Typically a solid, color may vary (usually off - white to yellowish)
    Melting Point Specific value would need experimental determination, expected to be in the range of organic solid melting points
    Solubility In Water Low solubility in water as it is an aromatic compound with non - polar groups
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform, etc.
    Vapor Pressure Low vapor pressure due to its relatively high molecular weight and solid nature

    As an accredited 2-(Trifluoromethyl)-1-Iodo-4-Nitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of 2-(trifluoromethyl)-1-iodo-4-nitrobenzene in sealed, labeled chemical - grade vial.
    Storage 2-(Trifluoromethyl)-1-iodo-4-nitrobenzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, flames, and incompatible substances like strong oxidizers. Store it in a tightly - sealed container to prevent leakage and exposure to air and moisture, which could potentially lead to decomposition or reaction.
    Shipping 2-(Trifluoromethyl)-1-iodo-4 -nitrobenzene is shipped in sealed, corrosion - resistant containers. Special handling precautions are taken due to its chemical nature, ensuring safe transport in compliance with hazardous materials regulations.
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    2-(Trifluoromethyl)-1-Iodo-4-Nitrobenzene 2-(Trifluoromethyl)-1-Iodo-4-Nitrobenzene
    General Information
    Historical Development
    At the beginning of the 20th century, Western chemistry was on the rise, and many novel compounds appeared in the world. Among them was a substance called 2- (trifluoromethyl) -1-iodine-4-nitrobenzene. At that time, chemical research was in the ascendant, and the exploration of this compound began.
    Scientists worked hard with simple equipment and exquisite techniques to analyze its composition and explore its characteristics. Although the conditions are difficult, their enthusiasm has not diminished. With the passage of time, science and technology have advanced day by day, and instruments have become more refined. The understanding of 2- (trifluoromethyl) -1-iodine-4-nitrobenzene has deepened. Knowing its unique use in the field of organic synthesis can pave the way for the creation of new compounds. The historical evolution of this compound is just like a page in a long volume of chemical exploration, witnessing the unremitting pursuit and innovation of researchers.
    Product Overview
    2- (trifluoromethyl) -1-iodine-4-nitrobenzene
    Fu2- (trifluoromethyl) -1-iodine-4-nitrobenzene is a valuable compound in the field of organic synthesis. Its structure is unique. It is based on a benzene ring and is side-chained with trifluoromethyl, iodine atoms and nitro groups. This structure endows the substance with specific chemical properties.
    From the perspective of reactivity, the iodine atom has high activity and can be used as a leaving group in many nucleophilic substitution reactions to facilitate the introduction of other functional groups. Nitro has strong electron-absorbing properties, which can reduce the electron cloud density of the benzene ring, affect the reactivity of other substituents on the benzene ring, and can also participate in a series of reactions such as reduction. The existence of trifluoromethyl can significantly change the physical and chemical properties of molecules due to its strong electronegativity and unique spatial effects, such as improving the fat solubility of compounds.
    In the process of organic synthesis, 2- (trifluoromethyl) -1-iodine-4-nitrobenzene is often a key intermediate. Through various reaction pathways, complex and functional organic molecules can be constructed, which have potential application value in pharmaceutical chemistry, materials science and other fields.
    Physical & Chemical Properties
    There is now a substance called 2- (trifluoromethyl) -1-iodine-4-nitrobenzene. The physical and chemical properties of this substance are quite important to our chemical researchers.
    Looking at its physical properties, it may be a solid state at room temperature, and its color and state may be unique. The values of its melting point and boiling point are related to its state changes in different temperature environments. Furthermore, the solubility of this substance in common solvents is also regular, or soluble in some organic solvents, or insoluble in water, which is determined by its molecular structure.
    In terms of its chemical properties, its chemical activity should not be underestimated because it contains functional groups such as nitro groups, iodine atoms and trifluoromethyl groups. Nitro groups are highly oxidizing or can participate in many redox reactions. Iodine atoms are active and prone to substitution reactions, providing the possibility for organic synthesis. The existence of trifluoromethyl groups gives molecules unique electronic and spatial effects, which affect their reactivity and selectivity. These properties are of great significance in the fields of organic synthesis and drug development, and should be further explored.
    Technical Specifications & Labeling
    Today there is a product named 2- (trifluoromethyl) -1-iodine-4-nitrobenzene. In terms of process specifications and identification (product parameters), our generation should pay attention to it in detail.
    The preparation of this product requires precise methods. From the selection of raw materials to the control of reaction conditions, there should be no difference. The temperature and pressure of the reaction, as well as the ratio of the reactants, are all key. And when operating, adhere to the standardized process to ensure the purity and quality of the product.
    As for the identification, the product parameters should be detailed. Its chemical composition, physical properties, hazardous characteristics, etc. should be clearly marked one by one. In this way, the user can understand its properties, make good use of it, and ensure the safety of production, storage and transportation. Process specifications and labels are crucial to the quality of products.
    Preparation Method
    The method of preparing 2 - (trifluoromethyl) -1 - iodine - 4 - nitrobenzene is essential for raw materials and processes. First, take suitable aromatic hydrocarbons, combine them with fluorine-containing reagents in a specific ratio, control the temperature within a certain range, and then react with substitution to obtain aromatic hydrocarbons containing trifluoromethyl.
    Then, based on this product, prepare with an iodizing agent, and under the condition of catalysis, perform the step of iodization to make the iodine atom just fit into the specified position. At the same time, pay attention to the rate and process of the reaction, and adjust the temperature and pressure in a timely manner.
    As for the nitrification stage, the aforementioned product is co-placed with the nitrifying reagent in a precise temperature control environment, so that the nitro group is introduced, and then 2- (trifluoromethyl) -1-iodine-4-nitrobenzene is formed. During this preparation process, the reaction steps are closely linked, and the reaction conditions must be strictly controlled to obtain high-quality products.
    Chemical Reactions & Modifications
    The chemical reaction and modification of (2 - (trifluoromethyl) - 1 - iodine - 4 - nitrobenzene) are particularly crucial.
    The chemical reaction of the husband is the way of material transformation. (2 - (trifluoromethyl) - 1 - iodine - 4 - nitrobenzene) has a unique structure and can be changed depending on the reaction conditions. Or at a suitable temperature and pressure, accompanied by a specific catalyst, the iodine group, nitro group or trifluoromethyl group can be substituted and added. The delicacy of this reaction lies in precise control to achieve the desired product.
    As for modification, in order to optimize its performance. The structure can be adjusted by reaction to make its physical and chemical properties more suitable. Such as enhancing stability, or changing its solubility, for special purposes.
    Looking at the reaction and modification of this chemical product, it is like exploring the unknown territory. Although the road is long and difficult, every new gain adds to the chemical palace, which is of great significance in industry, scientific research and other aspects.
    Synonyms & Product Names
    The name "2- (trifluoromethyl) -1-iodine-4-nitrobenzene" in the chemical industry today has a wide range of uses. However, its title may have similarities and differences.
    Although there is no such precise chemical naming in ancient times, it has long been related to material exploration. Today's material is an important material in chemical synthesis, pharmaceutical research and development, etc. Its similarities and differences are related to industry inheritance and regional differences.
    In the way of synthesis, this material is the key material, which can lead to various reactions and form various products. The aliases of its different names also change slightly due to the differences used by craftsmen and Fang families. Either according to its nature or according to its shape, the titles have their own wonders. And the name of the merchant also wants to recognize its uniqueness, which is different from other things, so there are many people with the same thing and different names. Although the names are different, the nature is the same, all of which are indispensable for promoting the progress of chemistry and the prosperity of industry.
    Safety & Operational Standards
    2 - (trifluoromethyl) -1 - iodine - 4 - nitrobenzene, this chemical substance is related to safety and operating standards, and is extremely important. It should be discussed in detail.
    In terms of safety, this substance is dangerous. It contains trifluoromethyl, nitro and other groups, or it may be toxic, irritating and corrosive. If you accidentally come into contact with the skin, rinse with plenty of water as soon as possible, and seek medical treatment to prevent skin damage and ulceration. If splashed into the eyes, you need to immediately open the eyelids, rinse with flowing water or normal saline, and then rush to the doctor to avoid serious eye injury. If its volatile gas is inhaled, it can cause respiratory discomfort or even poisoning. Therefore, it is necessary to ensure good ventilation during operation, or wear effective protective equipment.
    When talking about the operation specifications, the first storage should be cautious. It should be placed in a cool, dry and ventilated place, away from fire and heat sources, and avoid direct sunlight. Because of its active chemical properties, it needs to be stored separately from oxidants, reducing agents, acids, alkalis, etc., and must not be mixed to prevent dangerous chemical reactions.
    The operation process also has strict requirements. Experimental personnel must be professionally trained and familiar with the operation process and emergency treatment methods. Protective clothing, gloves, goggles and other protective equipment should be worn during operation. When taking this substance, a precise measuring tool should be used, and it should be accurately measured according to the experimental requirements to avoid waste and danger caused by excess. During the reaction process, the temperature, pressure, reaction time and other conditions should be strictly controlled, and the reaction process should be closely monitored to prevent runaway.
    In short, for 2- (trifluoromethyl) -1-iodine-4-nitrobenzene, safety and operation standards must not be ignored, which is the key to ensuring the safety of personnel and the smooth progress of the experiment.
    Application Area
    Fu2- (trifluoromethyl) -1-iodine-4-nitrobenzene is also a chemical substance. Its use, in the field of, can be used to make special effects, to
    With its characteristics, it can prevent pests and diseases, increase the prosperity of crops, and ensure the harvest of food. This is the use of 2- (trifluoromethyl) -1-iodine-4-nitrobenzene, which involves multiple fields, and is a step in promoting development, benefiting people's livelihood.
    Research & Development
    Today there is a thing called 2- (trifluoromethyl) -1-iodine-4-nitrobenzene, and I have gained something from its research. The properties of this thing are unique, and in the field of chemical research, it is quite valuable to explore.
    At the beginning of the research, its structure was carefully observed to clarify its chemical properties. After various experiments, its reaction mechanism was analyzed, and a better synthesis path was desired. Although the initial synthesis method is available, the yield is not ideal, and the steps are cumbersome.
    So I tried my best to improve it. Adjust the reaction conditions and select suitable reagents, so that the yield is finally increased and the process is simplified. In this process, we can gain insight into many influencing factors, such as temperature, pressure, and the proportion of reactants, which are all related to the quality and quantity of the product.
    Looking to the future, this product may shine in the fields of medicine, materials, etc. I should continue to study and expand its application scope, hoping to contribute to the development of the chemical industry, and promote it to a new realm, so as to achieve a perfect realm.
    Toxicity Research
    In this world, those who study chemicals should carefully examine their toxicity to ensure the safety of all living beings. Today, there is 2- (trifluoromethyl) -1-iodine-4-nitrobenzene, and our generation should carefully explore its toxicity.
    Look at its molecular structure, containing fluorine, iodine, and nitro groups. Fluorine is active, and its introduction or chemical activity changes; iodine atoms have specific electronic effects; nitro is also a strong electron-absorbing group, and the three are co-constructed, or have unique toxicological properties.
    To clarify its toxicity, a series of experiments should be conducted. First, cell experiments are used to observe its impact on cell growth and metabolism, and to see if it causes apoptosis and necrosis. Then animal experiments were used to explore the toxicity of its oral, percutaneous, inhalation and other routes, and to observe the damage to the functions of various organs in the body.
    Through these studies, the toxicity mystery of 2- (trifluoromethyl) -1-iodine-4-nitrobenzene can be known, providing a solid basis for the safety measures of its production, use and storage, and ensuring the safety of people and the environment.
    Future Prospects
    In the unfinished world, the way of chemical transformation is improving day by day. Today, there is a thing named 2- (trifluoromethyl) -1-iodine-4-nitrobenzene, which contains high energy. This compound is particularly special, or can be used in new research to cure the diseases of the world. In the field of materials, it is also expected to create amazing materials, create extraordinary materials, and increase their performance, resistance and other properties.
    Let's wait for our experts, diligently research, and sweat with wisdom to dig its deep secrets. In the next few days, we will definitely be able to use it to the best, promote the progress of world science and technology, and promote the well-being of the people, so that the unseen scene will be more successful in the present day, and we will go to the world of glory together.
    Where to Buy 2-(Trifluoromethyl)-1-Iodo-4-Nitrobenzene in China?
    As a trusted 2-(Trifluoromethyl)-1-Iodo-4-Nitrobenzene 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-(Trifluoromethyl)-1-Iodo-4-Nitrobenzene 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- (trifluoromethyl) -1-iodine-4-nitrobenzene?
    Ugh! In the matter of using plants, the most important thing is to use them. Madder, especially the importance of people. The main use of madder, can be too much.
    The first one can enter the disease. The nature of madder is bitter, cold, and the liver. It can remove blood, remove blood stasis, stop bleeding, and pass. In ancient times, in case of hemoptysis, vomiting blood, blood, urine, blood in the stool, leakage, stasis, bruising and other symptoms, madder is often used. If the treatment of vomiting blood is not stopped, you can use one madder, and then disperse it. Take two, one medium in water, fry until seven minutes, let it cool, and take it.
    Second, madder can be used for dyeing. Its root contains pigments such as Alizarin, which can be used to dye natural dyes. In ancient times, people often dyed cloth with madder, and the color dyed lasted for a long time. "Official"

    "The color dyed by madder is very important for dyeing. The color dyed by madder is very special, and it is used by the world.
    Furthermore, madder also has special meaning in some cultures and folklore. Or used for sacrifice, or as auspicious things. It is used for tools, dyeing, but it also contains the feelings and beliefs of the ancients.
    Of course, madder has an important role in dyeing, dyeing, etc. Its function is to save people's suffering, beautiful clothes, and add a lot of color to the lives of the ancients, and to the plants of heaven and earth.
    What are the physical properties of 2- (trifluoromethyl) -1-iodine-4-nitrobenzene?
    The trialkyl group is also a chemical group. Tetracyanobenzene, its physical properties are quite specific.
    Tetracyanobenzene is in a solid state, and its color is often white to light yellow, like the purity of the first snow in winter or the elegance of the afterglow of the autumn sun. The melting point of this substance is quite high, about a certain temperature range, and it requires a specific amount of energy to make it from solid to liquid, just like a stubborn stone needs to be calcined by fire to melt.
    Its density also has a certain value, and it contains a specific mass in a unit volume, just like measuring the thickness of an object. In common organic solvents, tetracyanobenzene exhibits unique solubility, or solubility, or slightly solubility, depending on the type of solvent, just like people with different personalities have different adaptations to different environments.
    In addition, the crystal structure of tetracyanobenzene is unique, and its internal atoms are arranged in an orderly manner, like a delicate chess game. Each atom interacts at a specific position to form a stable structure. This structure also affects its many physical properties, such as optical properties. In terms of optics, tetracyanobenzene absorbs or reflects light of a specific wavelength, resulting in corresponding optical phenomena, or shines shimmer, or shows a different color, just like a gem blooming under the light. These are all important physical properties of tetracyanobenzene, which are indispensable in chemical research and related fields.
    What are the chemical properties of 2- (trifluoromethyl) -1-iodine-4-nitrobenzene?
    The chemical properties of triethyl-1-amine-4-guanidine indole are very unique. The appearance of this compound may be colorless to yellowish, and it is mostly liquid at room temperature, but it may vary slightly due to changes in the surrounding environment.
    In terms of solubility, it often shows good solubility in polar solvents, such as alcohols and ethers. Because of its molecular structure, there are nitrogen-containing groups, which can interact with polar solvent molecules through hydrogen bonds, etc., so they are soluble. And in organic solvents, it may participate in a variety of chemical reactions, such as the reaction of nucleophilic substitution, the lone pair of electrons on the nitrogen atom, which makes it nucleophilic and can attack the electrophilic reagent, and then form new compounds.
    In terms of thermal stability, the substance can be relatively stable within a moderate temperature range. However, if the temperature is too high, its structure may be affected and changes such as decomposition occur. The process of decomposition, or the breaking of chemical bonds, produces a variety of small molecule products.
    Its acidity and alkalinity are also worth noting. Due to the existence of guanidine groups, this substance may be weakly basic. In aqueous solutions, it can be combined with protons to exhibit alkali properties. This alkaline property can play a key role in many chemical reactions and biological processes. For example, in some acid-base catalyzed reactions, it can be used as a base catalyst to promote the reaction.
    In redox reactions, the compound may exhibit certain characteristics. Some chemical bonds within the molecule may be broken or formed under the action of appropriate oxidants or reducing agents, resulting in changes in the structure and properties of the compound.
    All these chemical properties are interrelated and contain potential application value in chemical synthesis, drug development and other fields, which is worthy of further investigation.
    What is the synthesis method of 2- (trifluoromethyl) -1-iodine-4-nitrobenzene?
    The synthesis of triethyl-1-alkynyl-4-cyanobenzene is an important matter in organic synthesis. There are many methods, and the following are all common methods.
    First, halobenzene can be used. First take halobenzene and make it undergo a nucleophilic substitution reaction with triethylacetynyl lithium. In this reaction, the carbon anion of triethylacetynyl lithium has strong nucleophilicity and can attack the carbon connected to the halogen atom of halobenzene. The halogen atom leaves, and then forms triethyl-substituted alkynylbenzene. Then, through the cyanylation step, a suitable cyanylation reagent, such as cuprous cyanide, works synergistically with the corresponding ligand to introduce a cyanyl group, and finally obtain triethyl-1-alkylene-4-cyanobenzene.
    Second, the phenylacetylene derivative is used as the starting material. First, the benzene ring of phenylacetylene is triethylated, and a suitable triethylation reagent, such as the combination of triethylborane and base, is selected. Triethyl is introduced into the benzene ring through electrophilic substitution or nucleophilic substitution. After that, the alkynyl group is cyanylated, or the addition reaction of the alkynyl group and the cyanylation reagent under catalytic conditions is used to achieve the purpose of introducing a cyanyl group, so as to synthesize the target product.
    Third, the coupling reaction strategy of transition metal catalysis is adopted. Using benzene derivatives containing halogen atoms, triethylacetylene derivatives and cyanylation reagents as raw materials, the target molecule is constructed through multi-step coupling reaction in the presence of transition metal catalysts such as palladium and nickel. For example, Sonogashira coupling reaction is performed first, so that halobenzene and triethylacetylene form triethylacetylbenzene intermediates, and then cyanylation coupling reaction is carried out to successfully prepare triethyl-1-ethylene-4-cyanobenzene. This method can precisely control the reaction check point and process with the help of the unique activity of transition metal catalysts, and improve the selectivity and yield of the reaction.
    What are the precautions for the storage and transportation of 2- (trifluoromethyl) -1-iodine-4-nitrobenzene?
    The seven orifices of the husband are the reasons for people's audio-visual food and rest, which are related to life, and should not be careless. In today's discussion of amber in storage and transportation, there are three important ones, which are detailed as follows.
    First, amber is brittle and afraid of bumping. Although its quality is strong, it is easy to crack and damage when it is hit or dropped. Therefore, when storing, it should be placed in a soft-padded container, such as a velvet brocade box, to prevent the objects from colliding with each other. During transportation, it should also be wrapped in soft layers and properly fixed, so that the road cannot be hurt even if it is bumpy.
    Second, amber is afraid of high temperature and strong light. Under high temperature, amber is easy to soften and deform, and the strong light shines for a long time, and its color fades easily, which damages its beauty and value. The storage place should be cool and dry, protected from direct sunlight, and the temperature should be kept moderate and not too high. When transporting, you should also choose a cool season. If it is hot in the summer, you must have a cooling strategy, such as accompanied by ice packs or placed in a cool place in the carriage, so as not to expose it to the hot sun.
    Third, amber should avoid chemicals. Perfume, cosmetics, detergents, etc. contain many chemicals. When in contact with amber, it is easy to cause chemical reactions, erode its surface, and lose its luster. When storing, do not store with such substances. During transportation, also prevent it from being contaminated with chemicals. If you accidentally touch it, wash it with water and dry it as soon as possible.
    To sum up, amber storage and transportation must be carefully cared for to prevent bumps, avoid high temperatures, strong light, and chemicals, so as to keep it intact, preserve its rare quality, and pass on its beauty through the ages.