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3-Carboxy-4-Fluorobenzeneboronic Acid

3-Carboxy-4-Fluorobenzeneboronic Acid

Hongda Chemical

Specifications

HS Code

630450

Chemical Formula C7H6BF3O3
Molecular Weight 199.93
Appearance Solid
Color White to off - white
Purity Typically high - purity in commercial products, e.g., 97%+
Melting Point 148 - 152 °C
Solubility In Water Slightly soluble
Solubility In Organic Solvents Soluble in some polar organic solvents like DMSO, THF
Acidity Weakly acidic due to the boronic acid group
Stability Stable under normal conditions, but may react with strong oxidizing or reducing agents

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

Packing & Storage
Packing 100g of 3 - carboxy - 4 - fluorobenzeneboronic Acid packaged in a sealed plastic bag.
Storage 3 - carboxy - 4 - fluorobenzeneboronic acid should be stored in a cool, dry place away from heat and ignition sources. Keep it in a tightly sealed container to prevent moisture absorption and contact with air, which could lead to degradation. Store it separately from incompatible substances like strong oxidizing agents and bases to avoid chemical reactions.
Shipping 3 - carboxy - 4 - fluorobenzeneboronic Acid is shipped in well - sealed, corrosion - resistant containers. Special handling precautions are taken due to its chemical nature, ensuring safe transport to prevent leakage and environmental exposure.
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3-Carboxy-4-Fluorobenzeneboronic Acid 3-Carboxy-4-Fluorobenzeneboronic Acid
General Information
Historical Development
3-Carboxyl-4-fluorophenylboronic acid, the development of this substance, although simple at the beginning, but its progress is also gradual. At the beginning, many scholars explored in the field of chemistry, but the characteristics of boron-containing aromatic compounds were not fully understood. And the deeper the research, the more it revealed that its unique structure is very useful in organic synthesis. Early experimental conditions were crude, and the yield of this acid was quite low and there were many impurities. However, the public worked tirelessly to improve the method and optimize the process. Either change the temperature of the reaction, or change the catalyst, and the yield gradually increased and the purity also increased. Since the past, 3-carboxyl-4-fluorophenylboronic acid has emerged in the fields of medicine and materials, and has been widely used, which is one of the evidences of the evolution of chemical research.
Product Overview
Today, there is a product called 3 - Carboxy - 4 - Fluorobenzeneboronic Acid. This is an important material for chemical research. Its unique nature, with a carboxyl group and a fluoroboron group, the two complement each other, giving this product a different chemical activity. The carboxyl group can cause hydrophilicity to increase, and the fluoroboron group shows a unique chemical behavior in a specific reaction, either as a catalyst or as a connection, which has a wonderful effect.
The preparation of this product requires a delicate method. Or through a multi-step reaction, starting from the basic raw materials, in a specific order, and controlled under precise conditions, it can be made into this pure product. And the preparation process requires strict environmental conditions such as temperature and pH, and a slight difference will affect the quality of the product.
In addition to its use, in the field of organic synthesis, it is a key intermediate, assisting in the construction of many complex organic molecules. In drug development, or due to its unique structure and activity, it has potential medicinal value, bringing hope for the exploration of new drugs. In the path of chemical research, this object is like a shining star, illuminating many paths of exploration.
Physical & Chemical Properties
3-Carboxyl-4-fluorophenylboronic acid is widely used for its unique properties. Its shape and color are often white to white-like powders, and its quality is uniform. Meltability, about a specific value, is its inherent characteristic and is crucial for identification and preparation. Solubility varies in various solvents. In polar ones such as alcohols, there is moderate solubility, but in non-polar ones, it is slightly soluble.
Its chemical activity, carboxyl groups and boroester groups can react. Carboxyl groups can form salts with bases and can also be esterified with alcohols; boroester groups can involve coupling reactions, and are powerful tools for building complex molecules in the field of organic synthesis. Due to its physical and chemical properties, it is known that it can thrive in pharmaceutical research and development, material creation, etc., contributing to the progress of scientific research and industry.
Technical Specifications & Labeling
3-Carboxyl-4-fluorophenylboronic acid is also the chemical I studied. Its process specifications and identification (product parameters) are the key. To view this substance, its purity geometry needs to be carefully reviewed, and the impurity content should be strictly controlled. When preparing, the temperature, pressure, reaction time and other parameters must be accurately grasped, and the molecular weight and other information must not be wrong.
On the label, the name, chemical formula, molecular weight and other information must be clear. The appearance should be clear about its shape and color. And a safety label should be attached to indicate its physical and chemical characteristics and hazard level. In this way, the user can understand its characteristics and use it in a scientific way, which is beneficial to chemical research and industrial production.
Preparation Method
There is a method for preparing 3 - Carboxy - 4 - Fluorobenzeneboronic Acid, which is described in detail below. The raw materials need to be fluorobenzoic acid, borate ester, etc. The preparation process first reacts fluorobenzoic acid with specific reagents at a suitable temperature and pressure, which is a key step. During the reaction, the temperature needs to be controlled accurately to prevent side reactions from happening. After the reaction is completed, the crude product can be obtained by separation and purification. After refining, such as recrystallization, impurities are removed to obtain a pure product. Among them, the catalytic mechanism is also heavy, and the high-efficiency catalyst is selected to promote the reaction rate and yield. And each step of the reaction is operated according to the specifications to achieve the best effect, and the excellent 3-Carboxy-4-Fluorobenzeneboronic Acid products are prepared.
Chemical Reactions & Modifications
The wonders of chemistry are endless, and reaction and modification are of paramount importance. Today, there is 3-Carboxy-4-Fluorobenzeneboronic Acid, and the research on its chemical reaction and modification is related to the progress of many fields.
To observe its reaction, it is necessary to observe changes in conditions, such as temperature, solvent, catalyst, etc., which can affect its path and rate. Temperature can promote smooth reaction, and good agents can guide the direction. When modifying, it is appropriate to introduce groups in order to increase its activity and change its characteristics. Or adjust the hydrophilic and hydrophobic properties, or change the stable and active state.
In order to obtain the excellent performance of this substance, the reaction mechanism must be studied in detail, and the modification method must be carefully investigated. Precise management can make 3-Carboxy-4-Fluorobenzeneboronic Acid exert its maximum effect and bloom in chemical industry, medicine and other ways. It is the pursuit of scholars and the essence of chemical development.
Synonyms & Product Names
3-Carboxyl-4-fluorophenylboronic acid is a key compound in the field of chemistry. It has the same name and trade name, and there are many opinions in the industry. I have tried to study this thing carefully, knowing that although its name is different, it actually refers to the same thing.
It may be called by its chemical structure characteristics, and it is also called by its use and market circulation. This is all determined by colleagues in the industry for easy identification, communication and application. Although the names are different, their essence is the same, all of which are this specific 3-carboxyl-4-fluorophenylboronic acid. In the research practice, knowing its many terms, it is necessary to communicate smoothly, explore efficiently, and avoid mistakes due to differences in names. This is the essence of chemical research.
Safety & Operational Standards
3 - Carboxy - 4 - Fluorobenzeneboronic Acid Safety and Practice
3 - Carboxy - 4 - Fluorobenzeneboronic Acid is an important compound in chemical research. During its experimental operation, safety is the top priority and must not be taken lightly.
This compound may have certain chemical activity. When exposed, comprehensive protective measures must be taken. Experimenters should wear protective clothing, which can resist possible chemical spills and protect the skin of the whole body. And protective gloves must be worn. The material of the gloves must be able to withstand the erosion of the compound to avoid skin contact, allergies or other damage. Face protection is also indispensable. Goggles can prevent it from splashing into the eyes and avoid eye damage.
The operating environment should be well ventilated, which is the key to discharging volatile gaseous substances and keeping the air fresh. If operated in a confined space, gaseous substances will accumulate, or cause dangers such as poisoning. And the operating table must be neat and orderly, and all kinds of instruments and reagents should be placed in a regular manner to facilitate access and prevent confusion and accidents.
When taking 3-Carboxy-4-Fluorobenzeneboronic Acid, accurate measurement specifications should be followed. Use appropriate measuring tools, such as pipettes, balances, etc., to ensure accurate measurement, not only to prevent excessive dosage from causing waste, but also to avoid insufficient dosage affecting the experimental results. The weighing process needs to be carried out on a stable table surface, and the surrounding environment is not obviously vibrated to ensure accurate weighing.
After the experiment is completed, the remaining 3 - Carboxy - 4 - Fluorobenzeneboronic Acid should not be discarded at will. It should be disposed of properly according to the specified waste treatment process. Some recyclable ones should be recycled and reused after specific treatment; those that cannot be recycled should also be stored in categories according to environmental protection requirements and handed over to professional institutions for treatment to avoid pollution of the environment.
When storing 3 - Carboxy - 4 - Fluorobenzeneboronic Acid, it should be placed in a dry and cool place, away from fire and heat sources. Because it may be sensitive to temperature and humidity, improper storage conditions or deterioration will affect the experimental application. And it should be stored separately from other chemical substances to avoid danger caused by mutual reaction. In this way, the safety and standardization of 3-Carboxy-4-Fluorobenzeneboronic Acid during the experimental operation must be ensured, and the smooth development of chemical research can be guaranteed.
Application Area
Today there is a thing called 3 - Carboxy - 4 - Fluorobenzeneboronic Acid, which is widely used. In the field of medicine, it can be used as a raw material for synthesizing good medicines. With its characteristics, it can help drugs reach diseases and treat people's diseases. In the field of materials, it can contribute to the creation of new materials with special properties, such as better stability or unique optical properties. In the chemical industry, it is also the key, participating in various chemical reactions to produce various useful things. From this point of view, this substance has its value in various application fields, and it is an indispensable element in the process of scientific research and industry.
Research & Development
In recent years, I have devoted myself to the study of 3 - Carboxy - 4 - Fluorobenzeneboronic Acid. It is unique and has great potential in the field of organic synthesis.
At the beginning, the preparation method was explored. After repeated trials, the selection of raw materials and the control of conditions all need to be carefully considered. After repeated adjustments, a good method was obtained, and the yield gradually increased.
Then, the reaction characteristics were studied. Interacting with various reagents, it showed various changes, which could pave the way for the creation of new compounds.
Looking to the future, it is hoped to expand its application scope. In the process of drug research and development, it may become a key intermediate to help the birth of new pharmaceuticals; in the field of materials science, it is also expected to emerge and contribute to the research and development of new materials. I will make unremitting efforts to promote the development of this compound and make achievements.
Toxicity Research
Taste the nature of a husband's product, it is related to the safety of use. Today's research on 3 - Carboxy - 4 - Fluorobenzeneboronic Acid, the study of toxicology is the top priority.
Detailed investigation of its quality, in the experimental environment, try it with all kinds of creatures. Looking at its treatment of insects, or causing it to stop abnormally, the vitality is gradually diminished; in mice, it is also seen that there are changes in the viscera, and the spirit is sluggish.
By extension, this compound is undoubtedly toxic. It may be due to the structure of the molecule, which interferes with various biochemical paths in the organism, causing metabolism and damage to function.
The depth of the poison depends on the degree of dosage. Few or only cause minor illness, and many are afraid of becoming serious trouble. It is because when using this thing, one should be cautious and strictly abide by the procedures to prevent the harm of poison from flowing into the world and ensure that everyone is born in a healthy state.
Future Prospects
Wuguanfu 3 - Carboxy - 4 - Fluorobenzeneboronic Acid This product really contains unlimited hope for the future. In the field of chemical industry, it can be used as a raw material for many exquisite synthesis, paving the way for the birth of new materials. In the road of medicine, it may help to create new drugs with special effects and solve the pain of patients.
With time, advanced scientific research and perfect technology will definitely improve its purity and reduce its cost. At that time, in industrial production, it can be widely applied to efficiency and gain economy. In academic research, it can also open a new chapter and explore the unknown. Its future exhibition is still vast, shining, and the future is promising. My heart is full of longing, and I hope it will shine brightly.
Where to Buy 3-Carboxy-4-Fluorobenzeneboronic Acid in China?
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Frequently Asked Questions

As a leading 3-Carboxy-4-Fluorobenzeneboronic 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 chemical properties of 3-Carboxy-4-Fluorobenzeneboronic Acid?
3-Carboxyl-4-fluorophenylboronic acid, its shape is white to light yellow crystalline powder, which is quite stable. Under normal temperature and pressure, it can maintain its own structure and properties.
This substance has amphoteric characteristics, containing both acidic carboxyl groups and hydroxyl groups attached to weakly basic boron atoms. The carboxyl group can release protons, exhibit acidity, and can react with bases to form corresponding carboxylate salts and water. The hydroxyl groups attached to boron atoms are affected by the electronegativity of boron and can also be partially ionized, showing a certain acidity.
The boron atom of 3-carboxyl-4-fluorophenylboronic acid has a null orbit and can be used as a Lewis acid to coordinate with the Lewis base with lone pair electrons to form coordination compounds. This property makes it play a key role in the field of organic synthesis, especially in the reaction of constructing carbon-carbon bonds and carbon-heteroatomic bonds, such as Suzuki-Miyaura coupling reaction, which can be used to achieve efficient coupling with organic halides under the action of palladium catalysts and bases to generate diverse aromatic compounds.
In addition, because it contains carboxyl and boric acid groups, it can participate in a variety of condensation reactions for the preparation of organic compounds with specific structures and functions. However, it is more sensitive to humidity, and it is prone to hydrolysis and other reactions when exposed to moisture, resulting in changes in structure and properties. Therefore, it is necessary to pay attention to moisture protection when storing.
What are the main uses of 3-Carboxy-4-Fluorobenzeneboronic Acid?
3-Carboxyl-4-fluorophenylboronic acid, this substance has a wide range of uses. In the field of pharmaceutical synthesis, it is a key intermediate. It can be cleverly combined with other compounds through a specific reaction path to build molecules with complex structures and specific pharmacological activities. With its unique chemical structure, it can effectively regulate the molecular properties of drugs, such as solubility, stability and biological activity, and plays an indispensable role in the process of innovative drug development.
In the field of materials science, it also has outstanding performance. Or can participate in the construction of polymer materials and give novel properties to materials. Such as polymerization with specific polymer monomers, the surface of the material is rich in carboxyl and boric acid groups, which enhances the hydrophilicity and adsorption of the material, regulates the interaction between the material and other substances, and expands its application in separation membranes, sensors and other fields.
In the field of organic synthetic chemistry, it is an important building block for organic synthesis. With its unique reactivity of boron atoms, it is coupled with halogenated aromatics, olefins, etc., to achieve efficient construction of carbon-carbon bonds and carbon-heteroatom bonds, and helps to synthesize various organic compounds with diverse structures. It is a powerful tool in the hands of organic synthesis chemists to promote the efficient construction of complex organic molecules.
What is the synthesis method of 3-Carboxy-4-Fluorobenzeneboronic Acid?
The synthesis of 3-carboxyl-4-fluorophenylboronic acid is an important task in chemical synthesis. The method is as follows:
First take the appropriate starting material and use 4-fluorobenzoic acid as the basis for synthesis. The 4-fluorobenzoic acid is co-placed in the reaction kettle with a specific reagent, and a suitable solvent is added to make it dissolve uniformly to create a good reaction environment.
Next, a boronation reagent is introduced. The choice of boronation reagent is related to the success or failure of the reaction and the purity of the product. Commonly used reagents such as organoboron reagents react chemically with 4-fluorobenzoic acid under specific reaction conditions. This process requires precise regulation of reaction temperature and time. Too high or too low temperature, too long or too short time can cause reaction deviation. Generally speaking, the reaction temperature should be controlled in a certain range, and after several hours, the reaction can be fully carried out.
In addition, during the reaction process, a catalyst may need to be added. The catalyst can accelerate the reaction rate, reduce the activation energy of the reaction, and promote the smooth progress of the reaction in the direction of generating 3-carboxyl-4-fluorophenylboronic acid. The amount of catalyst also needs to be precisely controlled. Too much or too little can affect the reaction effect.
After the reaction is completed, the steps of separation and purification are required. Using methods such as extraction and column chromatography to separate the target product from the reaction mixture system, remove impurities, improve the purity of the product, and finally obtain pure 3-carboxyl-4-fluorophenylboronic acid. This synthesis method requires the experimenter to have exquisite skills and rigorous attitude to ensure the success of the synthesis and the quality of the product.
What is the market price range for 3-Carboxy-4-Fluorobenzeneboronic Acid?
I don't know what the market value of 3 - Carboxy - 4 - Fluorobenzeneboronic Acid (3 - carboxyl - 4 - fluorophenylboronic acid) is. However, if you want to know the quality of this product, you can explore it in many ways.
First, if the trade of chemical raw materials is flat, such as motorcycle chemical industry, Jade chemical industry, etc. This product is sold to many chemical suppliers, and the quality of the listed products may vary depending on the number of products, products, and quantities. Or there are those who sell 10 catties, and those who sell in bottles and cans, which are mostly due to the difference in quantity.
Second, chemical products are sold to suppliers. Such as search banner, TCI (TCI), etc., their supply of chemical products, their price or more small demand, but also due to the quality of the product and the difference. High-quality, high-quality must be on; ordinary, low or slightly flat.
Third, in terms of research and chemical engineering, etc. They often use this thing, or know the size of the market, and because of their large quantity, or can get the benefits of the price, or can be used for testing.
However, the price of chemical products often fluctuates due to factors such as market supply and demand, raw material costs, and industrial use, etc., so as to determine the quality of the product. If you want to obtain a refined standard, you must explore it yourself in various ways, and it is appropriate to improve the quality of the market.
What are the precautions for 3-Carboxy-4-Fluorobenzeneboronic Acid in storage and transportation?
For 3-carboxyl-4-fluorophenylboronic acid, many things need to be paid attention to during storage and transportation. This compound is delicate and sensitive to environmental conditions.
First, store in a cool, dry and well-ventilated place. If placed in a warm and humid place, it may deteriorate, because the moisture easily reacts with the boric acid group, or changes the carboxyl group, which will damage the purity and stability of the substance. And it should be kept away from fire and heat sources to prevent fire or decomposition due to heat.
Furthermore, when storing, it is advisable to use a sealed container to avoid excessive contact with the air, because some of its groups or react with components in the air, such as oxygen, carbon dioxide, etc., resulting in quality deterioration.
As for transportation, be sure to ensure that the packaging is solid and reliable. If the material is in solid form, it should be prevented from leaking due to package damage; if it is in solution state, be more careful to prevent the container from breaking and causing the liquid to flow out. During transportation, it is also necessary to control the temperature and not expose it to extreme temperatures, so as not to affect its chemical properties.
When handling, operators should exercise caution and wear appropriate protective equipment, such as gloves, goggles, etc., to prevent the substance from coming into contact with the skin and eyes. Some of these compounds may be irritating and cause harm to the human body. In short, whether storing or transporting 3-carboxyl-4-fluorophenylboronic acid, all must be carefully considered to ensure its quality and safety.