Hongda Chemical
Products
Home  /  Products  / 

2,3,4,5-Tetrafluorobenzeneboronic Acid

2,3,4,5-Tetrafluorobenzeneboronic Acid

Hongda Chemical

    Specifications

    HS Code

    693645

    Name 2,3,4,5-Tetrafluorobenzeneboronic Acid
    Molecular Formula C6H3BF4O2
    Molecular Weight 193.9
    Appearance White to off-white solid
    Cas Number 139404-44-9
    Purity Typically high purity for synthesis use
    Solubility Soluble in some organic solvents like DMSO
    Melting Point 142 - 146 °C
    Stability Air and moisture sensitive
    Application Used in organic synthesis for C-C bond formation

    As an accredited 2,3,4,5-Tetrafluorobenzeneboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of 2,3,4,5 - tetrafluorobenzeneboronic Acid in a sealed, chemical - resistant bottle.
    Storage 2,3,4,5 - Tetrafluorobenzeneboronic acid should be stored in a cool, dry place. Keep it in a tightly - sealed container to prevent moisture absorption, as boronic acids can react with water. Avoid storing near heat sources or incompatible substances. Store it in a well - ventilated area away from direct sunlight to maintain its stability and prevent decomposition.
    Shipping 2,3,4,5 - tetrafluorobenzeneboronic acid is shipped in well - sealed containers, compliant with chemical transportation regulations. Packaging safeguards the product from moisture and damage during transit to ensure safe delivery.
    Free Quote

    Competitive 2,3,4,5-Tetrafluorobenzeneboronic Acid prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615365186327 or mail to info@alchemist-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615365186327

    Email: info@alchemist-chem.com

    2,3,4,5-Tetrafluorobenzeneboronic Acid 2,3,4,5-Tetrafluorobenzeneboronic Acid
    General Information
    Historical Development
    "On the Development of 2,3,4,5-Tetrafluorophenylboronic Acid"
    The husband of 2,3,4,5-tetrafluorophenylboronic acid is also an important product of chemistry. Its origin originated from the study of various sages. At the beginning, the road of exploration was long, and it was not easy to obtain this product. The public worked hard and went through countless experiments before they achieved small success.
    Years have passed, and the technology has become more and more exquisite. The method of preparation in the past was cumbersome and inefficient, but after being improved by the wise, it became more and more simple. With the deepening of research, its application has also become more and more extensive, and it has emerged in the fields of medicine and materials.
    Looking at its development path, it is like a boat going against the water. If you don't advance, you will retreat. All the scientific researchers have worked hard to break through many difficulties with fearless courage, so that this product has been little known to the chemical industry. In fact, everyone has worked together to promote its evolution, so that it has today's grand scene.
    Product Overview
    2,3,4,5-tetrafluorophenylboronic acid is also an important agent in organic synthesis. Its color is pure and good quality, and it is widely used in medicine, electronics and other fields. Looking at its structure, fluorine atoms on the benzene ring are arranged in an orderly manner, and boric acid groups are connected to it, giving it unique chemical activity.
    Preparation of this product follows a specific method and goes through several delicate processes to meet the requirements of high purity. The reaction conditions need to be precisely controlled, and the temperature and reagent ratio are all about success or failure.
    In pharmaceutical research and development, it can be used as a key intermediate to help create new drugs and cure various diseases. In the electronics industry, it is also necessary for the manufacture of high-end materials to improve the performance of electronic components.
    This 2,3,4,5-tetrafluorophenylboronic acid, with its outstanding characteristics, is exhibiting an extraordinary posture on the stage of the modern chemical industry, contributing to the progress of science and technology and the development of the industry.
    Physical & Chemical Properties
    The physicochemical properties of 2,3,4,5-tetrafluorophenylboronic acid are worth exploring. Looking at its properties, it may be a white to off-white solid at room temperature, with a certain crystalline form. In terms of its melting point, or in a specific temperature range, this temperature characteristic is crucial for the identification and purification process. In terms of solubility, it may have a certain solubility in some organic solvents, but it may vary in water, which is related to its dispersion in different reaction systems and the degree of participation in the reaction. Its chemical stability cannot be ignored. Under common chemical environments, it may be able to maintain its own structure relatively stable. When encountering specific reagents or conditions, corresponding chemical reactions will occur, or new compounds will be formed, providing various possibilities for the field of chemical synthesis.
    Technical Specifications & Labeling
    "Technical Specifications and Labeling (Product Parameters) of 2,3,4,5-Tetrafluorophenylboronic Acid"
    There are currently 2,3,4,5-Tetrafluorophenylboronic Acid, and its technical specifications are related to many things. The synthesis method requires precise steps, temperature control, timing control and selection of appropriate raw materials and reagents, and follow a specific process to obtain products with good purity.
    In terms of identification, product parameters must be clear. Purity needs to meet specific standards, and impurity content is strictly limited. On the packaging, key information such as the name, chemical formula, purity, batch number, etc. of the product should be clearly stated for identification and traceability.
    Only in this way can 2,3,4,5-tetrafluorophenylboronic acid be guaranteed in quality when applied, and it is also convenient for all links to follow the specifications.
    Preparation Method
    The method of preparing 2,3,4,5-tetrafluorobenzene boronic acid is related to the raw materials and production process, reaction steps and catalytic mechanism. First, an appropriate amount of fluorobenzene is taken as the starting material, and after halogenation, halogen atoms are introduced to precisely regulate the reaction conditions, such as temperature, pressure and catalyst dosage. This is a key step.
    Next, the Grignard reagent method is used to react halogenated fluorobenzene with magnesium to make Grignard reagent. It needs to be operated in an anhydrous and anaerobic environment to prevent side reactions. After that, the Grignard reagent meets the borate ester, and through a series of reactions, the crude product of 2,3,4,5-tetrafluorobenzene boronic acid is obtained.
    Purified by recrystallization and other methods to obtain high-purity In this process, the proportion of raw materials, reaction time, and temperature changes need to be carefully controlled to ensure the smooth operation of each step. The catalyst accelerates and directs the key reaction, promoting the reaction to proceed efficiently towards the target product.
    Chemical Reactions & Modifications
    In recent times, chemical refinement has led to the frequent emergence of various new compounds. In this article, the chemical reactions and modifications of 2,3,4,5-Tetrafluorobenzeneboronic Acid are worth exploring.
    To understand its reaction, its structure needs to be investigated. This compound contains a fluorobenzene ring and a boric acid group. Fluorine has strong electronegativity, which reduces the electron cloud density of the benzene ring and affects the electrophilic substitution reaction. Its boric acid group is nucleophilic and can participate in many coupling reactions, such as Suzuki-Miyaura coupling, bonding with halogenated aromatics catalyzed by palladium. This reaction has mild conditions and high selectivity, and is widely used in the field of organic synthesis.
    As for modification, different substituents can be introduced. Modification with alkyl groups can modify its solubility and steric resistance, affecting its reactivity. The introduction of nitrogen-containing heterocycles may endow it with special electronic properties and coordination capabilities. The purpose of modification is to optimize its properties and make it better in the fields of materials science, drug research and development. Chemistry is constantly exploring such reactions and modifications to expand the boundaries of material applications.
    Synonyms & Product Names
    I heard that there is a thing, the name is 2, 3, 4, 5 - Tetrafluorobenzeneboronic Acid. This is a chemical thing, which is quite important in the industry. Its synonyms and trade names are also elegant.
    covers all things in the world, and the title often has similarities and differences. The synonyms of this chemical product are based on the chemical structure, properties and other reasons. There are different appellations, all of which refer to this thing accurately. As for the trade name, it is mostly due to market, use, promotion, etc. Businesses give it a unique name to distinguish it from others, to recognize its characteristics and facilitate its sales.
    Although the names are different, they all refer to this 2,3,4,5 - Tetrafluorobenzeneboronic Acid. For chemical researchers, only by clarifying their synonyms and trade names can they be accurate and not confused when researching and applying, thus promoting the progress of chemical research and making it better serve various industries in society.
    Safety & Operational Standards
    2,3,4,5-Tetrafluorophenylboronic acid is also used in chemical research. Its safe operation is essential, and it cannot be ignored.
    This object has certain chemical properties, and the operation must follow the rules. In order to survive, it is advisable to use dry, dry, and well-connected places to avoid fire and smoke sources. The package should also be in good condition to prevent leakage.
    During the operation process, the operator should take appropriate precautions, such as anti-clothing, gloves, and eyes, to ensure their own safety. If the skin is accidentally connected, it should be washed with a lot of water immediately, and it is necessary to seek medical treatment. If it is in the eyes, it is even more necessary to wash with water immediately and quickly.
    Furthermore, the place where this object is used must be cleared to prevent harmful gatherings. After finishing, the objects and utensils used should be properly handled and should not be disposed of.
    Therefore, the safe operation of 2,3,4,5-tetrafluorophenylboronic acid is the cornerstone of ensuring human safety and safety. It must not be ignored, and it must be followed to avoid danger.
    Application Area
    2,3,4,5 - tetrafluorophenylboronic acid, which is useful in many fields. In the field of pharmaceutical synthesis, it can pave the way for the creation of novel drugs. With its unique reaction mechanism, it helps to build key molecular structures and contributes to the research and development of good drugs to overcome difficult diseases.
    In the field of materials science, it can participate in the preparation of special performance materials. Through ingenious chemical reactions, materials such as excellent photoelectric properties can be applied to advanced display technologies in the future to improve display effects.
    In the field of organic synthesis, it is like a precise key to open the door to the construction of complex organic molecules. With its unique chemical activity, it can precisely introduce functional groups at specific locations and synthesize organic compounds with exquisite structures, injecting vitality into the development of the fine chemical industry.
    Research & Development
    I am committed to the research of 2,3,4,5 - Tetrafluorobenzeneboronic Acid. This compound has unique properties and great potential in the field of organic synthesis. Initial research, exploring its structure and characteristics, scrutinizing the reaction mechanism, and unremitting experiments, striving to accurately grasp.
    After repeated research, the synthesis process has been improved, and the yield and purity have been improved. This achievement lays the foundation for its wide application. Looking to the future, it is expected to expand its application in drug research and development, materials science and other fields, and promote the development of related industries. I will uphold the spirit of research and continue to explore, hoping to contribute to the progress of this product, promote its continuous development, and bloom more brilliance.
    Toxicity Research
    Study on the toxicity of 2,3,4,5-tetrafluorophenylboronic acid
    In the study of chemical products, the study of heavy toxicity of pigments. Now looking at 2,3,4,5-tetrafluorophenylboronic acid, it is necessary to investigate its toxicity in detail.
    First, explore its chemical properties. The structure of 2,3,4,5-tetrafluorophenylboronic acid is unique, and the position of the fluorine atom and the state of the boron atom are related to its toxicity. Fluoride is very active, or it may cause the compound to play a specific reaction in the body.
    Times, investigate its effect on the organism. After testing, observe its effect on cells. In vitro cell culture, observe its effect on cell proliferation and morphological changes. If the cell growth is inhibited and the morphology is aberrant, it is proved that it is toxic. Review its effect on the animal body, and observe the behavior and physiological indicators of the animals. If the animal is sluggish and has signs of organ damage, it is also clear that it is toxic.
    Furthermore, investigate the mechanism of toxicity. Or because it interferes with cell metabolism, hinders the activity of enzymes; or damages the structure of cell membranes and disrupts the transportation of substances. To clarify its mechanism, we can find ways to prevent it.
    In summary, the toxicity of 2,3,4,5-tetrafluorophenylboronic acid is studied in detail, which is the key to its safe use and harm avoidance.
    Future Prospects
    I have tried to study chemical things, and now I think and 2, 3, 4, 5 - Tetrafluorobenzeneboronic Acid this product. Although it is not widely known at the moment, I look at its nature, it has a special quality and contains infinite possibilities.
    The future development of
    may emerge in the field of pharmaceutical creation. With its wonderful structure, it may be able to accurately target the source of disease, help the formation of new drugs, and eliminate diseases for the world. Or shine in the research and development of materials, improve the material properties, and make the utensils more tough and durable.
    This product is like uncut jade. Over time, after my generation's research, it will be able to glow with brilliance, seek well-being for the world, and open up a new world.
    Where to Buy 2,3,4,5-Tetrafluorobenzeneboronic Acid in China?
    As a trusted 2,3,4,5-Tetrafluorobenzeneboronic Acid manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
    Frequently Asked Questions

    As a leading 2,3,4,5-Tetrafluorobenzeneboronic Acid 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 application fields of 2,3,4,5-tetrafluorophenylboronic acid
    2% 2C3% 2C4% 2C5-tetraethylenestronic acid is an important organic compound. Its main application fields are quite extensive, as follows:
    In the field of medicine, this compound has a wide range of uses. Due to its unique chemical structure and physiological activity, it plays a significant role in the development of steroid hormone drugs. It can be used as a key intermediate for the synthesis of a variety of steroid drugs with specific physiological functions, such as some drugs with endocrine regulation effect, which can help the human body maintain hormone balance and have good therapeutic and conditioning effects on many diseases caused by hormone imbalance, such as irregular menstruation and menopausal syndrome.
    In the field of biological science research, 2% 2C3% 2C4% 2C5-tetraethylenestronic acid also plays an important role. Scientists often use it as a bioactive probe. By studying its interaction with various receptors in organisms, they can gain in-depth insight into important biological processes such as hormone regulation mechanisms and cell signaling pathways in organisms, providing key clues and theoretical basis for basic research in life sciences.
    In the field of agriculture, this acid is also used. Some studies have shown that the rational use of preparations containing this ingredient may have a positive impact on the growth and development of some crops. Or it can regulate plant hormone levels, promote plant growth, enhance plant stress resistance, such as improving plant resistance to drought, diseases and pests and other adverse environments, thereby helping to increase agricultural production and income.
    In summary, 2% 2C3% 2C4% 2C5-tetraethylenestronic acid has shown important application value in the fields of medicine, biological science research and agriculture. With the continuous progress of science and technology, its potential application field may be broader.
    What are the synthesis methods of 2,3,4,5-tetrafluorophenylboronic acid?
    The synthesis method of 2% 2C3% 2C4% 2C5-tetraene succinic acid covers various routes. We can start from the basic organic raw material and obtain it through a multi-step reaction.
    First, a suitable olefin compound can be selected as the starting material. First, the olefin undergoes an addition reaction and a specific functional group is introduced. For example, an olefin with a suitable carbon chain structure is selected and added to a halogen-containing reagent to form a halogenated hydrocarbon. This halogenated hydrocarbon can then react with a nucleophilic reagent to introduce a carboxyl-related group.
    Next, the introduced group can be modified and converted by means of esterification reaction. The reaction conditions, such as temperature and the use of catalysts, are carefully adjusted to promote the reaction to proceed in the desired direction.
    In addition, the cyclization reaction can also be considered to construct the basic skeleton of tetraethylsuccinic acid. For example, a compound containing a polyene structure is used as a substrate, and it is cyclized within the molecule to form a product with a specific ring system. Subsequently, the substituents on the ring are appropriately modified to achieve the purpose of generating tetraethylsuccinic acid.
    Or it is obtained from natural products and chemically modified. Some naturally occurring compounds have structures similar to tetraethylsuccinic acid, and their structures can be adjusted by chemical reactions such as hydrolysis, oxidation, and reduction to convert them into target products.
    During the synthesis process, it is crucial to control the reaction conditions. Temperature, pressure, reaction time, proportion of reactants and other factors will have a significant impact on the yield and selectivity of the reaction. After each step of the reaction, the product needs to be separated and purified to ensure the smooth progress of the next step. In this way, after many exquisite designs and careful operations, the effective synthesis of 2% 2C3% 2C4% 2C5-tetraene succinic acid can be achieved.
    What are the physical and chemical properties of 2,3,4,5-tetrafluorophenylboronic acid?
    2% 2C3% 2C4% 2C5-tetraethylenestronic acid is a genus of organic compounds. Its physical and chemical properties are quite specific, and this is what you are talking about in detail.
    In terms of its physical properties, this substance is in the shape of a solid state at room temperature. Looking at its appearance, it is usually white to light yellow crystalline powder, which is fine and uniform. Smell, the smell is very small, almost invisible. Its melting point is fixed, about within a certain temperature range. This property is quite crucial when identifying and purifying. And its solubility varies in common solvents. In organic solvents such as ethanol and acetone, it can have a certain solubility. However, in water, the solubility is very small, which is due to the characteristics of its molecular structure.
    As for the chemical properties, 2% 2C3% 2C4% 2C5-tetraethylenestronic acid has functional groups such as ethylenic bonds and carboxyl groups. The existence of ethylenic bonds allows it to participate in many addition reactions, such as with halogens, hydrogen halides and other electrophilic reagents, which can be successfully added to generate corresponding derivatives. The carboxyl group is active and can neutralize with bases to form carboxylic salts. In case of alcohols, under suitable catalytic conditions, esterification can occur to produce ester compounds. And because of its conjugated ethylene bond system, it may exhibit unique optical properties under light irradiation of a certain wavelength, which may have potential applications in the field of photochemistry. Its chemical stability also needs attention. In a specific temperature, humidity and pH environment, decomposition or other chemical reactions may occur, so when stored, it needs to be properly disposed of according to its characteristics.
    The physical and chemical properties of this substance are of great significance in many fields such as medicine and chemical industry, affecting its preparation, application and storage.
    What are the precautions for storing and transporting 2,3,4,5-tetrafluorophenylboronic acid?
    When storing and transporting 2% 2C3% 2C4% 2C5-tetraethylenestrone acid, many things need to be paid attention to.
    First of all, it is quite sensitive to temperature and humidity. This acid is suitable for storage in a cool and dry place, and the temperature should be controlled within a specific range to prevent high temperature from causing its properties to mutate, or the risk of deliquescence due to excessive humidity. If the temperature is too high, the molecular movement will intensify, or the chemical structure will be changed, resulting in damage to its quality. If the humidity is large, the water will be immersed, which will easily cause deterioration and affect its efficacy and stability.
    Second, light is also the key. 2% 2C3% 2C4% 2C5-tetraethylenestronic acid should be protected from direct light and stored in a container that is shaded from light. Light has energy, or induces luminescent chemical reactions, causing the acid to decompose or undergo other adverse changes, thereby reducing its active ingredients.
    Furthermore, during transportation, it is necessary to ensure that the packaging is intact. The packaging should be solid and reliable to prevent the container from being damaged due to bumps and collisions, causing 2% 2C3% 2C4% 2C5-tetraethylenestronic acid to leak. Once leaked, it will not only waste raw materials, but also cause pollution to the surrounding environment. What's more, if it comes into contact with the human body, it may endanger health.
    In addition, this acid may be contraindicated in compatibility with certain substances. In storage and transportation, do not mix with other substances. Otherwise, it may cause chemical reactions, cause its failure, or even generate harmful products.
    In addition, the storage place should be well ventilated. If the ventilation is poor, harmful gases will accumulate, or have adverse effects on 2% 2C3% 2C4% 2C5-tetraethylenestronic acid, and can reduce safety hazards and prevent accidents caused by high gas concentration.
    In short, 2% 2C3% 2C4% 2C5-tetraethylenestronic acid needs to be treated with caution in terms of temperature, humidity, light, packaging, compatibility and ventilation during storage and transportation to ensure its quality and safety.
    What is the market price range of 2,3,4,5-tetrafluorophenylboronic acid?
    2% 2C3% 2C4% 2C5-tetrahydrofuran butyric acid, which is an important organic compound in the field of fine chemicals, is widely used in medicine, coatings, adhesives and other industries. Its market price range often fluctuates due to factors such as quality, purity, market supply and demand.
    Under the heading, for general industrial-grade purity products, the price is roughly between several thousand yuan and more than 10,000 yuan per ton. If it is high purity, such as used in pharmaceutical research and development or high-end electronics, the price will rise sharply, up to tens of thousands of yuan per ton or even higher.
    Due to the vagaries of the chemical product market, the price of raw materials, the innovation of production processes, and the impact of policies and regulations will all cause price fluctuations. Therefore, if you want to know the exact price, you should consult professional chemical product suppliers and traders for details, or refer to the real-time quotation of professional chemical information platforms, in order to obtain the latest and accurate price information to meet the needs of commercial activities such as procurement or sales.