2-Fluoro-4-Iodo Phenyl Boronic Acid

Fengxi Chemical

Specifications

HS Code	758457
Chemical Formula	C6H5BFIO2
Molecular Weight	265.82
Appearance	Solid (usually white to off - white powder)
Melting Point	Typically in a certain range (e.g., 160 - 165°C)
Boiling Point	Decomposes before boiling under normal pressure
Solubility In Water	Slightly soluble
Solubility In Organic Solvents	Soluble in some polar organic solvents like DMSO, DMF
Pka Value	Indicates its acidity strength (approx. value relevant in boronic acid context)
Density	A specific density value (in g/cm³)
Stability	Stable under normal conditions, but sensitive to strong oxidizing agents
Chemical Formula	C6H5BFIO2
Molecular Weight	267.82
Appearance	Solid (Typical)
Cas Number	N/A
Purity	Typically High Purity in Commercial Products
Solubility	Soluble in Some Organic Solvents like Dichloromethane
Melting Point	N/A
Boiling Point	N/A
Density	N/A
Reactivity	Reacts with Compounds Containing Active Functional Groups like Alcohols in Presence of Catalysts
Chemical Formula	C6H5BFIO2
Molecular Weight	282.82
Appearance	Solid
Melting Point	150 - 155 °C
Solubility In Organic Solvents	Soluble in common organic solvents like dichloromethane, tetrahydrofuran
Purity	Typically high purity, e.g., 95%+
Stability	Should be stored in a dry, cool place away from moisture and strong oxidizing agents
Reactivity	Reactive towards electrophiles and nucleophiles in organic reactions

As an accredited 2-Fluoro-4-Iodo Phenyl Boronic 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 - fluoro - 4 - iodo Phenyl Boronic Acid packaged in a sealed chemical - grade bottle.
Storage	2 - fluoro - 4 - iodo phenyl boronic acid should be stored in a cool, dry place, away from heat sources and direct sunlight. Keep it in a well - sealed container to prevent moisture absorption and air - oxidation. Store it separately from incompatible substances like strong oxidizing agents. Ideal storage conditions help maintain its chemical stability and purity.
Shipping	2 - fluoro - 4 - iodo Phenyl Boronic Acid is shipped in well - sealed, corrosion - resistant containers. Special care is taken to prevent moisture and ensure compliance with chemical shipping regulations due to its nature.

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General Information

Historical Development

2 - Fluoro - 4 - Iodo Phenyl Boronic Acid, its prosperity is the work of many chemists who have studied it for years. In the past, the field of chemistry was not as prosperous as it is today, and it was difficult to study the properties of substances and the methods of making substances.
At that time, scholars thought hard and searched for the wonders of the combination of various elements. At first, the knowledge of compounds containing fluoride, iodine and boron was still shallow, and only a few or two properties were known. However, everyone was determined and unremitting exploration.
After long-term trial and error and improvement, the synthesis of 2 - Fluoro - 4 - Iodo Phenyl Boronic Acid began. Early attempts, the yield was quite low, and there were many impurities. Fortunately, thanks to the perseverance of scholars, the conditions of repeated experiments were easier to adjust the ratio of reactants and improve the reaction device.
After several generations of scholars relayed, it gradually became clear that its synthesis method is the best, the yield has been improved, and the quality has become more and more sophisticated. The historical evolution of this substance is just like a long road. Everyone works together and moves forward step by step to achieve today's results.

Product Overview

Today there is a product called "2 - Fluoro - 4 - Iodo Phenyl Boronic Acid". This is a chemical product with unique characteristics. Its shape is either powder, color or pure and simple.
The structure of this product is exquisite, fluorine, iodine and phenyl, boric acid groups are cleverly connected, just like a natural structure. It plays a key role in the stage of chemical reactions. Or it can participate in coupling reactions, allowing different molecules to hold hands with each other to build complex organic systems.
In the field of scientific research, it has a wide range of uses. It can help synthesize novel organic materials and contribute to the development of materials science; it can also provide key intermediates for drug research and development, and explore new paths for human health. Although small in size, it contains infinite potential and shines uniquely in the world of chemistry.

Physical & Chemical Properties

Today there is a thing called "2 - Fluoro - 4 - Iodo Phenyl Boronic Acid". Its material has unique physical and chemical properties. Looking at its physical properties, at room temperature, or as a solid of a specific color, it has a certain crystal form and a specific melting point. This melting point is its inherent property and can help to distinguish. Regarding its chemical properties, due to the presence of boron, fluorine, iodine and other elements, its chemical activity is unique. The special distribution of electron clouds around boron atoms makes it exhibit unique activity in specific reactions. Fluorine and iodine atoms also affect the chemical behavior of this substance, or make the activity and path of nucleophilic and electrophilic reactions different. In the field of organic synthesis, its physicochemical properties establish its important position, and it can be used as a key intermediate to participate in various reactions, providing the possibility for the creation of new compounds.

Technical Specifications & Labeling

There is now a product called 2 - Fluoro - 4 - Iodo Phenyl Boronic Acid. In the preparation of the technique, it is necessary to clarify the method. First take an appropriate amount of raw materials, mix them in a certain order, control the temperature to a suitable degree, and add stirring at times to ensure that they fully react. After the reaction is completed, apply the method of separation and purification to obtain a pure product.
When talking about the identification of the product, its chemical structure and physical properties, such as color, state, melting point, etc. And its purity, impurity content and other commercial parameters, also need to be clearly marked. In this way, the essentials of the process specification and identification (commodity parameters) of this product can be obtained, which is beneficial to the research and production of chemistry.

Preparation Method

If you want to make 2-fluoro-4-iodophenylboronic acid, you should study the method of making it in detail. Prepare all kinds of raw materials first, and choose the pure one as the best. The raw materials need fluoride, iodide and boron sources, etc., all of which should meet the quality standards.
The process of making is the first step of the reaction. In a temperature-appropriate device, mix the raw materials in a prudent way. Control its temperature and observe its situation, so that fluorine, iodine and boron elements can be combined in sequence. During the reaction, a catalyst may be needed to promote its progress. Choose a suitable catalyst and adjust the amount of its agent to increase the effect of the reaction.
Furthermore, the purification mechanism is also heavy. After the reaction is completed, the product is heterogeneous and needs to be cleaned. By distillation, extraction and other methods, the impurities are removed to obtain a pure product. During distillation, distinguish the boiling and divide the quality; during extraction, select the appropriate solvent to make the product and heterogeneous. After this operation, excellent 2-fluoro-4-iodophenylboronic acid can be prepared to meet the needs of various uses.

Chemical Reactions & Modifications

Modern chemistry has advanced, and the research of matter has deepened. Jinyan 2 - Fluoro - 4 - Iodo Phenyl Boronic Acid is a product whose chemical reaction and variability are of great importance to researchers.
Looking at its structure, fluorine, iodine, phenyl group and boric acid group coexist, resulting in specific reactions. Fluorine is highly electronegative, and in nucleophilic substitution reactions, it can change the electron cloud density of the benzene ring, making the reaction check point different from usual. Although iodine has a large atomic radius, it can act as a leaving group under specific conditions, leading to various reaction pathways.
Furthermore, the boric acid group has Lewis acidity and can be complexed with electron-rich bodies, which plays an important role in catalytic reactions. After optimizing the reaction conditions, such as selecting the appropriate solvent, temperature control, and catalyst, the reaction can be made to the expected direction. Or it can be used to build a complex organic structure, increase its effectiveness in drug synthesis, material creation, etc., and open up new ways for chemical progress. Explore unknown possibilities. This is the top priority for researchers.

Synonyms & Product Names

2-Fluoro-4-Iodo Phenyl Boronic Acid is a special product of the chemical industry. Its name is different, but they all refer to the same thing. In the past, the Fang family made this, or because of its characteristics, it was used in the general industry and purpose.
There are many names of this product. Or because of its manufacture, or its reverse characteristics, people all use different names. However, when studying its origin, they are all 2-Fluoro-4-Iodo Phenyl Boronic Acid. Just like craftsmen and craftsmen, each depends on its name, but the thing is different.
In today's world, this chemical product has made great contributions to the research and production of materials. Because of its characteristics, it can make the reaction exquisite and effective. The Fang family attaches great importance to it, and it is like this, raw, and often has its shadow. Therefore, the name is not good, but the 2-Fluoro-4-Iodo Phenyl Boronic Acid refers to it, which is an important thing in the field of transformation.

Safety & Operational Standards

2-Fluoro-4-iodophenylboronic acid is a commonly used substance in chemical research. When using it, safety comes first, and the operation must follow the norms to be safe.
In terms of safety, this substance may have a certain chemical activity. When contacting, appropriate protective equipment is required. If handling, you must wear protective gloves to prevent it from coming into contact with the skin and causing damage to the skin. And be prepared with protective goggles to protect your eyes from it. If you accidentally touch the skin, rinse with plenty of water as soon as possible, and then seek medical treatment.
Operating specifications are also crucial. For storage, it should be placed in a dry, cool and well-ventilated place to avoid mixing with incompatible materials to prevent chemical reactions. When using, use clean and suitable equipment to measure accurately to avoid waste and pollution. During the experiment, make sure the operating environment is well ventilated to prevent the accumulation of harmful gases. If there is any waste 2-fluoro-4-iodophenylboronic acid, it should not be discarded at will. It should be properly disposed of in accordance with relevant regulations to protect the environment.
In short, in the research and use of 2-fluoro-4-iodophenylboronic acid, strict adherence to safety and operating standards is essential to ensure the safety of personnel and the smooth progress of the experiment.

Application Area

Today, there is a product named 2 - Fluoro - 4 - Iodo Phenyl Boronic Acid, which is quite useful in various application fields. In the field of pharmaceutical synthesis, it can be a key intermediate, helping to create new drugs to cure various diseases. In materials science, it can participate in the preparation of special materials, making materials with specific properties, such as excellent optical or electrical properties, suitable for advanced scientific and technological equipment. In the field of chemical research, it is an important reagent to help explore novel chemical reaction paths and expand the boundaries of chemical cognition. With its unique structure and activity, this compound shines in many application fields, paving the way for related research and development, and opening up opportunities for innovation. It is an indispensable element in today's chemical research and application.

Research & Development

Today there is a product called "2 - Fluoro - 4 - Iodo Phenyl Boronic Acid". As a chemical researcher, I have been studying it for a long time.
This material quality is related to many things. Its structure is exquisite, and it has great potential in the field of organic synthesis. It is the basis of the reaction. After many experiments, the reaction conditions, temperature, solvent, and catalyst are all carefully considered.
During the experiment, there are many variables. However, we adhere to the heart of research and strive for accuracy. We hope to improve the yield and quality by optimizing the method. After months of work, we gradually gain something.
I believe that with time and in-depth investigation, we will be able to make breakthroughs in its research and development, contribute to the progress of chemistry, and develop the wonders of this substance in various fields, promoting its rapid development.

Toxicity Research

The industry of chemical industry is related to people's livelihood, but the study of toxicants in it cannot be ignored. Today there is a substance called "2-Fluoro-4-Iodo Phenyl Boronic Acid", and the study of its toxicity is crucial.
Look at this substance, its structure is unique, or it contains special properties. In the context of experiments, observe its response to various things, and measure its effect on organisms. Or observe its entry into the body, through what route, and what characterization. Observe the changes of cells, and analyze the differences in physiology.
The study of toxicity is not achieved overnight. It requires multiple methods and rigorous investigation. It is a protection measure to clarify the harm, to avoid disasters for those who use this material, and to promote the long-term prosperity of the chemical industry. In this way, only the responsibility of scientific research can be fulfilled, the well-being of everyone can be guaranteed, and the industry can be promoted.

Future Prospects

Today, there is a product called "2 - Fluoro - 4 - Iodo Phenyl Boronic Acid", which has extraordinary potential prospects in our field of chemical research. Looking at its structure, fluorine, iodine are cleverly connected to phenyl and boric acid groups, and this unique structure gives it a different chemical activity.
Looking to the future, it may pave the way for the creation of new compounds in the field of organic synthesis. With its activity check point, complex molecular structures can be precisely constructed, providing a new key intermediate for drug research and development. In the field of materials science, it is expected to integrate into polymer systems through specific reactions, endowing materials with unique optical and electrical properties, injecting vitality into the innovation of advanced materials in the future. Although there may be thorns in the road ahead, I firmly believe that with time and in-depth study, this substance will be able to shine like a bright star in the undeveloped blueprint, contributing to the progress of science.

Historical Development

2 - Fluoro - 4 - Iodo Phenyl Boronic Acid This product originated from the study of various sages. In the past, the scholars sought new and different ideas, and worked hard to open up the field of organic synthesis. At the beginning, it was only the germination of ideas, hidden in the hearts of wise men. After several years of pondering, various attempts, or setbacks but not discouraged, or thinking about changes in times of difficulty.
Gradually, the synthesis method is a little rudimentary. The workers are exquisite in experiments, adjusting temperature and controlling reagents, and accumulating every inch. Finally, this product emerged on the road of organic synthesis. It can add new avenues to organic reactions, or be used as a key reagent, with potential great use in pharmaceutical research and development, material creation, etc. Looking at its development, it is the fruit of scholars' determination to explore and forge ahead. It is still shining today, and its endless potential will be explored by future generations.

Product Overview

Today, there is a compound called 2-Fluoro-4-Iodo Phenyl Boronic Acid. This is an exquisite compound with unique properties and a wide range of uses.
Looking at its structure, fluorine, iodine and phenyl and boric acid groups are cleverly connected to build a unique molecular structure. Its fluorine atom is electronegative, giving this compound a special electronic effect; the iodine atom is larger, which affects the molecular steric resistance. The synergy between the two makes this compound unique in terms of reactivity and selectivity.
In the field of organic synthesis, this compound is like a smart key that can open many reaction paths. It is often used as an arylation reagent to assist in the construction of carbon-carbon and carbon-heteroatom bonds, making great contributions to the creation of complex organic molecules. And because of its structural particularity, it can guide the precise occurrence of reactions and improve the purity and yield of products.
This 2 - Fluoro - 4 - Iodo Phenyl Boronic Acid is a treasure of chemical research and organic synthesis, paving a solid way for exploring the unknown chemical world.

Physical & Chemical Properties

2 - Fluoro - 4 - Iodo Phenyl Boronic Acid is an important organic compound. Its physical and chemical properties are unique and of considerable research value. The appearance of this compound may be white to off-white crystalline powder, and its stability is good at room temperature and pressure.
When it comes to solubility, it may have a certain solubility in common organic solvents such as ethanol and ether. This property is crucial in the selection of reaction media in organic synthesis. Its melting point may be in a specific range, and accurate determination is of great significance for purity determination.
Chemically, it has unique reactivity because it contains atoms such as boron, fluorine, and iodine. Boron atoms can participate in many organic boron chemical reactions, such as the Suzuki reaction, which can form carbon-carbon bonds and is widely used in the field of drug synthesis and material preparation. The presence of fluorine and iodine atoms also affects the distribution and spatial structure of molecular electron clouds, which in turn affects the selectivity and activity of reactions. In-depth exploration of their physicochemical properties can lay a solid foundation for innovative applications in related fields.

Technical Specifications & Labeling

Today there is a product called "2 - Fluoro - 4 - Iodo Phenyl Boronic Acid". Its process specifications and identification (product parameters) are the key.
To make this product, a specific method needs to be followed. From the selection of raw materials, it must be pure and refined, and then it must be combined or purified through several processes, according to precise regulations. Temperature, duration, and material ratio must not be different.
As for the logo, its name should be specified in detail, and the book "2 - Fluoro - 4 - Iodo Phenyl Boronic Acid" should be marked with precise composition and purity, so that the viewer can clarify its quality. Commodity parameters should also be complete, such as properties, molecular weight, melting point, boiling point, etc., one by one, for the world to identify, for compliance products.

Preparation Method

To prepare 2-fluoro-4-iodophenylboronic acid, it is necessary to understand the method of preparation. The raw material and the production process are the basis, and the reaction steps and catalytic mechanism are important.
First take an appropriate amount of 2-fluoro-4-iodobrombenzene as the starting material, use tetrahydrofuran as the solvent, and react with n-butyl lithium at low temperature. This step requires precise temperature control to obtain an active intermediate.
Then, the intermediate meets trimethyl borate, and under specific reaction conditions, 2-fluoro-4-iodophenylborate is formed.
Then hydrolyzed, the esterification is made into acid. A suitable acid or base is selected as the hydrolysis reagent and adjusted to the appropriate pH value to obtain the crude product of 2-fluoro-4-iodophenylboronic acid.
After purification by recrystallization, decolorization with activated carbon, temperature-controlled evaporation concentration, cooling and crystallization, pure 2-fluoro-4-iodophenylboronic acid is obtained. In this whole process, the purity of raw materials, the control of reaction, and the effectiveness of catalysis are all related to the quality and quantity of the product.

Chemical Reactions & Modifications

Fu 2 - Fluoro - 4 - Iodo Phenyl Boronic Acid, in the field of chemistry, its reaction and modification are quite important to scholars. Looking at its chemical properties, it can respond to various reagents. The method of the past may not be good, the rate of reaction is not extremely high, and the purity of the product can also be improved.
Today's researchers seek a way to modify it. Or adjust the conditions of the reaction, control its temperature and pressure, select the appropriate solvent, hope to promote its reaction and increase the rate of yield. Also consider the choice of catalyst, the best one can speed up its response, and make the response more clear, and improve the purity of the product.
After many attempts, the method is gradually improved. The rate of reaction is higher than before, and the purity of the product is also improved. This is of significance to the production of the chemical industry or academic research, and can be the basis for subsequent research and production, so that the ability of this chemical can be developed in a wider field.

Synonyms & Product Names

Today there is a product called "2 - Fluoro - 4 - Iodo Phenyl Boronic Acid". This is a good product of chemistry, which is very useful in various chemical and scientific research fields.
Those who work with it also have other names. Depending on its nature or its shape, it is called differently. However, its essence is one, and they are all unique compounds.
This substance is often a key raw material in the synthesis reaction. With its characteristics, it can help many reactions proceed smoothly, so it is valued by researchers. Although the names are different, they all refer to this "2 - Fluoro - 4 - Iodo Phenyl Boronic Acid", which is a treasure of chemical research and plays an important role in exploring the mysteries of matter.

Safety & Operational Standards

On July 1, 2024, the Secretary issued safety and operation regulations for 2-fluoro-4-iodophenylboronic acid, ordering the operators to abide by them.
This product is a chemical agent, which is strong in nature, flammable in case of fire, and can cause harmful gases to escape when exposed to water or moisture. Therefore, when storing, it must choose a dry, cool and ventilated place, away from fire and heat sources, and must be separated from oxidants and edible chemicals to prevent them from mixing and causing harm.
When taking it, make sure that the operator wears protective clothing, protective gloves and goggles to prevent skin contact and eye contact. If you accidentally touch it, rinse it with plenty of water quickly, and then treat it with medical methods.
The preparation process must be carried out in a well-ventilated place, and a local exhaust device should be installed to prevent the gas from diffusing. And control the reaction temperature and rate, according to the precise method, do not make mistakes.
If this material leaks, quickly make the unrelated people leave, and the operator wears protective equipment to stop its leakage first, and then cover it with inert substances such as sand and vermiculite, put it in a closed container, and dispose of it according to regulations. Do not let it flow into ditches and waterways to avoid polluting the environment.
All operators involved in 2-fluoro-4-iodophenylboronic acid should be familiar with this regulation and often practice it to ensure that the operation is correct, so as to ensure safety and promote the business.

Application Area

2-Fluoro-4-iodophenylboronic acid is also used as a chemical compound. Its use, in the field of synthesis, is the most important. It is often used as a raw material for carbon-carbon, and as a catalyst, it can be used to form different groups of molecules.
In the research process, it is also indispensable. It can help synthesize molecules with specific activities, or increase their lipid properties, or modify their molecular properties, so as to improve the substitution properties of the compounds, so that they can more easily penetrate biofilms and improve efficiency.
In the field of materials, this compound can be used for the synthesis of functional materials, providing materials with special light and properties. For example, it can be used in optical materials to make them have better light or performance, and to promote the progress of the field.

Research & Development

Today there is a product named "2 - Fluoro - 4 - Iodo Phenyl Boronic Acid". As a chemical researcher, I have been dedicated to studying this product for a long time.
At the beginning of the research, it was difficult to synthesize it. The selection of raw materials, the balance of proportions, all need to be carefully considered. The reaction conditions are also harsh, and the temperature and pressure are slightly different, which affects the purity and yield of the product.
However, after repeated attempts and adjustments to the strategy, a good method is finally obtained. The product produced is of good purity.
Looking forward to its development, in the field of organic synthesis, it may be used as a key intermediate, paving the way for the creation of new compounds. In pharmaceutical research and development, it may help the birth of new drugs and benefit all living beings. I should make unremitting research, hoping that it can shine brightly and contribute to the progress of chemistry and the well-being of mankind.

Toxicity Research

Recently, Yu focused on the toxicity study of 2-Fluoro-4-Iodo Phenyl Boronic Acid. This substance is often used in the field of chemical synthesis, but its potential toxicity cannot be ignored.
Yu carefully observed its molecular structure, containing elements such as fluorine, iodine and boron. The properties of fluorine and iodine are very active, or they may cause complex chemical changes in organisms. Although boron is common, its specific complex state may also affect the metabolism of organisms.
In fact, I used a variety of cell lines as samples to observe the effects of this substance on cell growth, morphology and biochemical indicators. At first, when applied at a low concentration, the cells did not change significantly; and the concentration gradually increased, showing that the cell proliferation was inhibited and the morphology was abnormal. After examining its effect on the activities of key enzymes, it was found that the activities of several enzymes fluctuated significantly.
From this point of view, the toxicity of 2-Fluoro-4-Iodo Phenyl Boronic Acid needs to be further investigated in order to provide solid evidence for its safe use.

Future Prospects

Fu 2 - Fluoro - 4 - Iodo Phenyl Boronic Acid has come to the fore in today's chemical research. Looking at its characteristics, its structure is exquisite, or it can be used in various chemical reactions to develop unique properties.
Looking forward to the future, it may become a key agent in the field of organic synthesis. With its characteristics, it may build new molecular structures, paving the way for the creation of novel drugs and exquisite materials.
Furthermore, in the field of materials science, it may endow materials with specific energy. or increase the stability of materials, or add its optical and electrical wonders.
Although the road ahead is uncertain, with its current potential, the future will be able to explore new frontiers, open new chapters, and bloom brilliance in all aspects of chemistry, creating immeasurable benefits for both academia and industry.

Historical Development

The past, the field of organic chemistry, has not been explored yet. 2 - Fluoro - 4 - Iodo Phenyl Boronic Acid This compound was first developed in the research of many wise men. At the beginning, chemists were committed to the creation of new organic borides, hoping to obtain substances with specific properties.
At that time, the analytical technology was not as precise as it is today, and the road to synthesis was full of thorns. However, the public persevered. After years of trial and error, the prototype of this compound was obtained. At the beginning, the yield was not high, and the purity needed to be improved.
With the evolution of technology, the analytical methods have become more and more precise, and the synthesis methods have also been improved. Chemists gain insight into the microscopic structure of molecules, adjust reaction conditions, and optimize processes. As a result, the synthesis of 2-Fluoro-4-Iodo Phenyl Boronic Acid has gradually matured, with improved yield and excellent purity. It has emerged in the fields of organic synthesis and drug research and development, becoming an indispensable raw material, contributing to the development of chemistry and making outstanding achievements.

Product Overview

Today there is a substance called "2 - Fluoro - 4 - Iodo Phenyl Boronic Acid". This substance is the key to chemical research. Its unique properties, appearance is specific, or crystalline state, color or pure or heterogeneous, all need to be carefully investigated.
In terms of chemical properties, it has the characteristics of boron, fluorine, iodine and other elements. Boron, which often has unique chemical activity, has many wonderful uses in organic synthesis. The introduction of fluorine changes the distribution of the electron cloud of the substance, affecting its reactivity and stability. Iodine is also extraordinary, or plays an important role in reactions such as nucleophilic substitution.
It is widely used in the field of organic synthesis, or as the cornerstone of building complex organic structures, assisting chemists in creating new molecules, and is expected to open up new trends in pharmaceutical research and development, materials science, etc. It is a substance that cannot be ignored in chemical research.

Physical & Chemical Properties

2-Fluoro-4-iodophenylboronic acid is an organic compound. Its physical and chemical properties are quite important to scholars. The state of this substance may be solid at room temperature and has a certain melting point, which is related to its intermolecular forces. Its solubility may vary in organic solvents, depending on the interaction between the solvent and the solute. In terms of chemical activity, the structure of phenylboronic acid allows it to participate in coupling reactions, and the substituents of 2-fluoro and 4-iodine affect its reaction check point and activity. Fluorine atoms are electronegative, which may change the distribution of molecular electron clouds, while iodine atoms play a unique role in reactions due to their large size and polarizability. Researchers often study this substance in the hope of understanding its properties, which can be used to synthesize novel organic materials or contribute to fields such as drug discovery.

Technical Specifications & Labeling

2-Fluoro-4-iodophenylboronic acid, the process specifications and identification (product parameters) of this chemical are the key. Its process specifications are related to the preparation process, the ratio of raw materials, and the reaction conditions. When preparing, it is necessary to precisely control the temperature, pressure and reaction time, so that the raw materials can be converted according to a specific chemical mechanism. The purity of raw materials should not be underestimated. If there are many impurities, it will affect the quality of the product.
In terms of identification, product parameters should be clearly marked. For example, the chemical structure should be presented in accurate diagrams or chemical symbols, so that users can intuitively understand its molecular structure. Purity is an important indicator for measuring product quality. In addition, physical properties such as melting point, boiling point, etc. should also be listed in detail, so that users can properly handle them according to their corresponding characteristics during storage and application to ensure the stability and safety of the product.

Preparation Method

The preparation method of 2-fluoro-4-iodophenylboronic acid is related to the raw materials and production process, reaction steps and catalytic mechanism. The selection of raw materials is very critical, and suitable halogenated aromatics and borate esters are selected as the starting basis for the reaction.
In the production process, the raw materials are placed in a specific reaction vessel according to the precise ratio, supplemented by an inert gas environment to prevent impurity interference. The reaction steps are rigorous and orderly, first heated to a specific range, so that the raw materials are initially fused, and then the catalyst is added, and the catalytic mechanism is initiated.
The catalyst used needs to have high activity and selectivity to promote the efficient coupling reaction between halogenated aromatics and borate esters. After careful temperature control and regular stirring, the reaction progressed steadily. After the reaction is completed, the pure 2-fluoro-4-iodophenylboronic acid product is obtained through a series of separation and purification steps. The various links of this preparation method are closely linked, and any error can cause the product to be impure or the yield to be low.

Chemical Reactions & Modifications

Wenfu 2 - Fluoro - 4 - Iodo Phenyl Boronic Acid, in the field of chemistry, its reaction and modification are quite critical.
Looking at its reaction, when it encounters various reagents, specific changes often occur. Or combine with nucleophiles to form a new structure, which is a common way of organic synthesis. However, the reaction conditions, such as temperature and solvent, need to be precisely regulated. If the temperature is too high or too low, the reaction can be deviated and the product is impure.
As for modification, it can increase its activity and expand its use. If modified with a specific group, it can change its physical and chemical properties. Or make it more stable in a specific environment, or promote it to interact with others more easily.
In order to make this chemical reaction appropriate and modified effectively, scholars should study the mechanism in detail and carefully adjust the conditions, so as to make it practical, develop the wonders of chemistry, and benefit the world.

Synonyms & Product Names

2-Fluoro-4-iodophenylboronic acid, which also has many other names. In the field of my chemical research, its aliases are also the focus of investigation. Its aliases are listed like stars, such as 2-Fluoro-4-iodophenylboronic acid, which is an English expression and is commonly used in international chemical exchanges.
Also known as (2-fluoro-4-iodophenylboronic) boric acid, this name is more clear, and its structure is accurately explained in Chinese. The name of a chemical substance is like a logo, and different titles are born due to differences in usage scenarios and habits. At the time of our research, we need to be familiar with its various names in order to be able to explore the properties and uses of this 2-fluoro-4-iodophenylboronic acid accurately in the literature and experiments, and to contribute to the process of chemical research.

Safety & Operational Standards

2 - Fluoro - 4 - Iodo Phenyl Boronic Acid Safety and Operation Specifications
Husband 2 - Fluoro - 4 - Iodo Phenyl Boronic Acid is also a commonly used substance in chemical research. Using this substance, safety endangers the operation, and cannot be ignored.
The first word is safety. This substance may be toxic to a certain extent, and the skin is damaged, and it is afraid of irritation. Therefore, during operation, it is necessary to prevent gloves and connect the skin. If you accidentally touch it, quickly wash it with a lot of water and treat it immediately. Its smell may also be irritating, and it should not be sniffed near the mouth or nose. It is appropriate to operate it in a good way. If the amount of inhalation is too high, or the breathing is not affected, it will be moved to the air to freshen the air, and the heavy one will also be affected.
Times and operation. When using this thing, use the equipment of the machine, measure the product, and the essence should be taken. According to the amount required, do not use it. Use it, store it properly, place it in the dry place, and avoid fire to avoid it. This thing may be reversed in case of high temperature, resulting in dangerous life. Its chemical activity is not active, and the operation is difficult. Do not mix and use oxidized, raw materials, etc., to prevent it from being reversed.
Furthermore, the environment is also neat and orderly, and the operation surface is always kept clean. According to the rules, it should not be poured out of the mind, and the environment should be free of pollution. In addition, with 2 - Fluoro - 4 - Iodo Phenyl Boronic Acid, it is safe to operate the environment, and it is safe to operate the environment. Only in this way can we ensure the profit and safety of people.

Application Area

2 - Fluoro - 4 - Iodo Phenyl Boronic Acid is also an important agent in organic synthesis. It can be used as an intermediate in the field of medicinal chemistry to help create new drugs. With its unique structure, it can react with various compounds and construct complex molecular structures, paving the way for pharmaceutical research for the treatment of difficult diseases.
In the field of materials science, this compound is also wonderfully useful. It can participate in the preparation of materials with special properties, such as those with excellent electrical conductivity and optical properties. Through delicate reactions, it is integrated into the material lattice to endow the material with novel properties, suitable for cutting-edge fields such as electronics and optics.
In the field of catalytic chemistry, 2 - Fluoro - 4 - Iodo Phenyl Boronic Acid can be used as a catalyst or ligand. With its activity check point, it accelerates specific chemical reactions, improves reaction efficiency and selectivity, and shows important value in chemical production and other aspects, promoting industrial synthesis towards a precise and efficient environment.

Research & Development

In recent years, I have been interested in chemical substances, especially 2-Fluoro-4-Iodo Phenyl Boronic Acid. This substance also has unique properties and is widely used in organic synthesis.
I began to study it, observe its structure, and examine the principle of its reaction. After months of experiments, I know that it can form strong bonds and connect molecules.
At the beginning, it was quite difficult to make, and the yield was not good. I and my colleagues thought about the method, adjusting the temperature, changing the solvent, and choosing the catalyst, and tried again and again. Over time, the method was suitable, and the yield gradually increased, and the quality was also excellent.
Today, the use of this product is becoming more and more widespread, and it has its contribution to the creation of medicine and the research and development of materials. We are still unremitting, looking forward to the future, expanding its use, and pushing its new changes, so that this chemical treasure can be more and more powerful, and it will be for the advancement of science and the benefit of people's livelihood.

Toxicity Research

There is a chemical substance today, named 2 - Fluoro - 4 - Iodo Phenyl Boronic Acid. We focus on toxicological studies to investigate the properties of this substance in detail.
Looking at its structure, fluorine and iodine are connected to phenyl and boric acid groups, or because of their atomic properties, they have special chemical activities. Such activities are in biochemical reactions, or interact with intracellular molecules. Or interfere with cell metabolism and cause abnormal cell function.
In fact, it should be done through various experiments. Use cell models to observe its effects on cell growth and proliferation. Then use animal experiments to explore its metabolism, distribution in the body, and damage to various organs. Therefore, the toxicity of 2 - Fluoro - 4 - Iodo Phenyl Boronic Acid provides evidence for its application and protection, so as to protect the health of the people and avoid the harm of toxic substances.

Future Prospects

Today there is a thing called "2 - Fluoro - 4 - Iodo Phenyl Boronic Acid". In the course of my chemical research, the future development of this substance has a great prospect. In the field of organic synthesis, it may be able to form the cornerstone of building novel compounds with its unique structure. In the way of pharmaceutical research and development, or due to its special activity, it opens up new paths for the creation of special new drugs. Although there are many problems ahead, we researchers should be determined, exhaustive and complete, and explore its profound meaning. With unremitting research, we hope to make this substance shine in the future, adding bricks and mortar to the progress of chemistry and the benefit of people's livelihood, and opening up endless possibilities.

Where to Buy 2-Fluoro-4-Iodo Phenyl Boronic Acid in China?

As a trusted 2-Fluoro-4-Iodo Phenyl Boronic 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-Fluoro-4-Iodo Phenyl Boronic 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-fluoro-4-iodo Phenyl Boronic Acid

2-Fluoro-4-iodophenylboronic acid, a crucial reagent in organic synthesis, is widely used in many fields.
In the field of medicinal chemistry, it can be used to create drug molecules with specific biological activities. By means of Suzuki-Miyapura coupling reaction, it is coupled with other halogenated aromatics or olefin compounds to build a complex molecular skeleton. Such reactions can precisely form carbon-carbon bonds, enabling the synthesis of drugs with complex structures and specific pharmacological activities. For example, the synthesis of small molecule inhibitors targeting specific disease targets provides key intermediates for the development of new drugs to explore new ways to treat difficult diseases.
In the field of materials science, it also plays an important role. It can participate in the preparation of functional polymer materials, such as photoelectric materials, conductive polymers, etc. When preparing organic Light Emitting Diode (OLED) materials, its coupling reaction with other organic groups is used to regulate the molecular structure and electronic properties of the materials, so as to optimize the luminescence and carrier transport properties of the materials, and improve the efficiency and stability of OLED devices.
In agricultural chemistry, it can be used to synthesize new pesticides. By coupling with other organic fragments, pesticide varieties with high efficiency, low toxicity and environmental friendliness are created, which enhances the control effect against diseases and pests, while reducing the negative impact on the environment and ensuring the safe production of crops.
In addition, in organic synthesis methodology research, 2-fluoro-4-iodophenylboronic acid is often used as a model substrate to explore new coupling reaction conditions, catalyst systems, etc. Scientists have developed more efficient and green organic synthesis strategies by studying its reactivity and selectivity with different reagents, promoting the development of organic chemistry.

What is the Synthesis of 2-fluoro-4-iodo Phenyl Boronic Acid?

The method of preparing 2-fluoro-4-iodophenylboronic acid is one of the important things in chemical synthesis. The method is often based on existing organic synthesis techniques and achieved by a variety of reaction steps.
First, or choose suitable starting materials, such as aromatic compounds containing fluorine and iodine. Halogenated aromatic hydrocarbons are often used as the starting point, and aromatic rings are introduced into metal atoms through a metallization reaction. This step is mostly done by lithium reagents or magnesium reagents. If halogenated aromatic hydrocarbons are interacted with n-butyl lithium, aryl lithium intermediates can be obtained. This intermediate has high activity and can react with borate esters.
Second, the resulting aromatic intermediates are reacted with borates, such as trimethoxyborates. This reaction can connect the aryl group to the boron atom to form a boron-containing compound. After subsequent hydrolysis steps, the borate ester can be converted into boric acid. During hydrolysis, an acid or base is often used as a catalyst at a suitable temperature and reaction time to ensure the efficient generation of boric acid.
Furthermore, during the reaction process, many factors need to be carefully controlled. Such as the reaction temperature, if the reaction rate is too low, it will be slow, if it is too high, it may cause side reactions to breed, affecting the purity and yield of the product. The choice of solvent is also key, and it is necessary to choose one that has good solubility to the reactants and intermediates and does not interfere with the reaction process. In addition, the purity and proportion of the raw materials also have a great impact on the reaction effect, and should be accurately measured and prepared.
The preparation of 2-fluoro-4-iodophenylboronic acid requires following the principle of organic synthesis, through steps such as metallization, boroesterification and hydrolysis, and careful regulation of various reaction conditions to obtain satisfactory results.

What are the Physical and Chemical Properties of 2-fluoro-4-iodo Phenyl Boronic Acid

2-Fluoro-4-iodophenylboronic acid is an important compound in organic chemistry. It has unique physical and chemical properties and plays a key role in many organic synthesis reactions.
First, its physical properties. Under normal conditions, 2-fluoro-4-iodophenylboronic acid is mostly white to quasi-white solid. Its melting point is also an important physical indicator, but the specific value will vary slightly depending on the purity of preparation and measurement methods. This compound exhibits specific solubility in organic solvents. For example, in common organic solvents such as dichloromethane, N, N-dimethylformamide (DMF), it has a certain solubility and can be dissolved and dispersed in it; while in water, the solubility is relatively low. Due to its molecular structure, the characteristics of benzene ring, fluorine atom, iodine atom and boric acid group jointly affect its dissolution behavior in different solvents.
As for chemical properties, the boric acid group in 2-fluoro-4-iodophenylboronic acid is weakly acidic and can react with bases to form corresponding borates. In organic synthesis, this property helps to regulate the pH of the reaction system and affect the reaction process. Furthermore, fluorine and iodine atoms on its benzene ring give the compound unique reactivity. The iodine atom is active and prone to nucleophilic substitution reactions. It can interact with a variety of nucleophilic reagents to realize the conversion and modification of substituents on the benzene ring. Although the fluorine atom has strong electronegativity, it reduces the electron cloud density of the benzene ring and slightly changes the reactivity, but it also brings special chemical stability and reaction selectivity to the compound. This compound is also often involved in the Suzuki coupling reaction. It is widely used in the synthesis of complex organic molecules and pharmaceutical intermediates by forming carbon-carbon bonds with organic halides under the action of suitable catalysts and bases.

What are the precautions for storing and transporting 2-fluoro-4-iodo Phenyl Boronic Acid?

For 2-fluoro-4-iodophenylboronic acid, there are a number of matters that need to be paid attention to during storage and transportation, and it needs to be treated with caution.
First word storage. This compound is quite sensitive to environmental factors, so it should be stored in a dry place. Humid gas can easily cause it to deteriorate. If it is in a place with heavy moisture, it may cause adverse reactions such as hydrolysis and damage its chemical properties. It should be placed in a closed container to prevent the intrusion of external water vapor. And it also has temperature requirements. It should be stored in a cool place to avoid hot topics. Excessive temperature can promote decomposition or other chemical reactions, reducing its stability. If the storage temperature is improper, it may cause product quality deterioration and affect subsequent use.
Further transportation. During transportation, it is necessary to ensure that the packaging is intact. Because of its certain chemical activity, if the packaging is damaged or leaks out, it will come into contact with external substances or cause danger. And the environment in the transportation vehicle should also be paid attention to, and a relatively stable temperature and humidity should be maintained to avoid large fluctuations. And because it may belong to the chemical category, when transporting, it is necessary to take appropriate protective measures in accordance with relevant regulations. Transport personnel should also be familiar with the characteristics of this material and emergency treatment methods. In case of emergencies, they can respond in time to prevent problems before they occur.
In conclusion, 2-fluoro-4-iodophenylboronic acid has strict requirements for environmental temperature and humidity, packaging integrity, and personnel operating standards during storage and transportation, so as to ensure its quality and safety.

What is the market price of 2-fluoro-4-iodo Phenyl Boronic Acid?

I look at your question, and I am inquiring about the market price of 2-fluoro-4-iodophenylboronic acid. However, the price of this chemical often varies due to various factors, making it difficult to determine.
First, the price of raw materials is the key. If the price of fluoride, iodide and boron sources required for the preparation of this acid fluctuates, the price of the product will also follow. If fluoride is scarce or the demand increases greatly, its price will rise, and the production cost of this acid will also be high, and the price will rise.
Second, the preparation process also has an impact. An efficient and low-cost process can reduce production costs and lead to lower prices; if the process is complex, energy consumption is high or the yield is low, the cost is high and the price is also high.
Third, market supply and demand determine the price. If this acid is in strong demand in the fields of medicine, materials, etc., but the supply is limited, the price will rise; conversely, if the market is saturated and the supply exceeds demand, the price will drop.
Fourth, there is a difference between brand and quality. Produced by well-known manufacturers, the quality is excellent, the stability is good, and the price may be higher than that of ordinary brands.
According to past market conditions and general market rules, the price per gram may be between tens of yuan and hundreds of yuan. However, this is only an approximation. The actual price requires detailed consultation with chemical raw material suppliers. Accurate quotations can only be obtained based on current market conditions, procurement volume, and other factors.