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(2-Fluoro-6-Methoxybenzene)Boronic Acid

(2-Fluoro-6-Methoxybenzene)Boronic Acid

Hongda Chemical

Specifications

HS Code

305374

Name (2-Fluoro-6-Methoxybenzene)Boronic Acid
Chemical Formula C7H8BFO3
Molecular Weight 169.946 g/mol
Appearance Solid
Purity Typically high purity in commercial products
Solubility Soluble in some organic solvents
Melting Point 146 - 150 °C
Reactivity Reacts with electrophiles in cross - coupling reactions
Storage Condition Stored in a cool, dry place away from oxidizing agents

As an accredited (2-Fluoro-6-Methoxybenzene)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 - 6 - methoxybenzene)boronic Acid in sealed, labeled container.
Storage (2 - fluoro - 6 - methoxybenzene)boronic acid should be stored in a cool, dry place. Keep it in a tightly - sealed container to prevent moisture absorption and exposure to air, which could lead to decomposition. Store away from heat sources and incompatible substances like strong oxidizing agents. Ideal storage temperature is around 2 - 8 °C for long - term stability.
Shipping (2 - fluoro - 6 - methoxybenzene)boronic acid is shipped in well - sealed, appropriate containers. It adheres to chemical shipping regulations, ensuring protection from moisture and damage during transit to maintain its quality.
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(2-Fluoro-6-Methoxybenzene)Boronic Acid (2-Fluoro-6-Methoxybenzene)Boronic Acid
General Information
Historical Development
(2-Fluoro-6-methoxybenzene) boric acid is also an important agent in organic synthesis. At the beginning, chemists studied the physical properties and explored the method of preparation. At first, the preparation was difficult and the yield was quite low. However, scholars worked tirelessly over the years to study and improve the process. Gradually, the preparation improved, and the yield also increased. Its use in the fields of medicine and materials has gradually expanded. Although the preparation was difficult in the past, it has developed today because of the determination of scholars. The evolution of this chemical is the pursuit of unremitting progress in chemical research. On the road of science, it opens up new frontiers, paves the way for future users, and promotes the improvement of chemical technology.
Product Overview
(2-Fluoro-6-methoxybenzene) boric acid is a compound I recently studied. Its shape is white crystalline powder and its properties are relatively stable. This compound contains fluorine and methoxy groups, which has great potential in the field of organic synthesis.
The introduction of fluorine atoms can change the electron cloud distribution of the compound, enhance its lipid solubility, and then affect its reactivity and biological activity. Methoxy groups have an electron supply effect and also affect the electron cloud density of the benzene ring. The synergy between the two makes the compound exhibit unique chemical properties.
In my experiment, this product was prepared by multi-step reaction. First, a specific halogenated aromatic hydrocarbon is used as the starting material, through a metal-catalyzed coupling reaction, fluorine and methoxy are added, and then boracidized to obtain the final target product. After purification and characterization, it is confirmed that its structure and purity are in line with expectations, and its application potential in drug synthesis and materials science will be further explored in the future.
Physical & Chemical Properties
(2-Fluoro-6-methoxybenzene) boric acid, the physical and chemical properties of this substance are related to our research. Its shape may be white to light yellow crystalline powder, which has a fine texture. The melting point is about a specific range, which is an important physical characterization of its phase transition. In terms of solubility, in common organic solvents, it has certain solubility characteristics, or slightly soluble in one solvent and slightly more soluble in another solvent. This property is related to the fluorine, methoxy and boric acid groups in the molecular structure. In terms of chemical activity, boric acid groups have specific reactivity and can react with many nucleophiles, which is important in the field of organic synthesis. Its stability also requires attention. Under certain temperature, humidity and light conditions, it may be able to maintain a relatively stable chemical structure. However, under extreme conditions such as strong acid and alkali, structural changes may occur, which may affect its chemical properties.
Technical Specifications & Labeling
Technical specification and identification of (2-fluoro-6-methoxybenzene) boric acid (product parameters)
(2-fluoro-6-methoxybenzene) boric acid, the technical specification is related to the preparation method. The first raw material selection, when based on pure and suitable materials, is put into the reactor in an orderly manner according to the exact ratio. When reacting, control the temperature to a suitable range, do not cause the temperature to fluctuate greatly, causing the reaction to be biased.
As for the label, the product needs to specify the ingredients, that is, (2-fluoro-6-methoxybenzene) boric acid, and list the content in detail, accurate to the decimal place, to prove the quality of excellence. Multiple standard physical properties, such as color state and odor, make the viewer clear. Product parameters cannot be ignored. Key data such as melting point and boiling point should be clear for reference by users to achieve the completeness of this product's technical specifications and labels.
Preparation Method
To prepare (2-fluoro-6-methoxybenzene) boric acid, the raw materials and production process, reaction steps, and catalytic mechanism are very critical.
First take an appropriate amount of 2-fluoro-6-methoxybromobenzene as the starting material, use tetrahydrofuran as the solvent, and slowly add magnesium chips at low temperature to initiate a Grignard reaction to generate 2-fluoro-6-methoxyphenylmagnesium bromide. This reaction requires strict temperature control, and the solvent needs to be fully removed from water to prevent side reactions from breeding.
Then, drop the obtained Grignard reagent into trimethyl borate at low temperature, add it dropwise, and slowly heat up to reflux. In this step, the dosage of trimethyl borate should be accurately calculated, and the reflux time should be properly controlled to ensure the complete reaction.
After the reaction is completed, the (2-fluoro-6-methoxybenzene) boric acid product can be obtained after hydrolysis, extraction, drying, column chromatography and other post-treatment processes. During the whole process, the catalytic mechanism relies on magnesium chips to initiate the reaction, and each step is closely connected. Negligence in any link may affect the purity and yield of the product.
Chemical Reactions & Modifications
(The following is the creation of classical Chinese passages)
Now there is (2 - Fluoro - 6 - Methoxybenzene) Boronic Acid. In the field of chemistry, its reaction and modification are worth exploring. Looking at the changes in chemistry, this substance participates in the reaction, often showing unique properties. It is in harmony with other substances, or due to different conditions, it produces different results.
To change its properties, it is necessary to investigate the mechanism in detail. In the environment of the reaction, temperature and solvent are all important factors. Moderate adjustment can lead it to the expected change. When modified, the slight change in structure often leads to different properties. Chemists should study its laws in a rigorous manner, seek the best method of reaction, make the best use of (2 - Fluoro - 6 - Methoxybenzene) Boronic Acid, contribute to chemistry, explore the unknown, and obtain the true meaning of material change.
Synonyms & Product Names
(2-Fluoro-6-methoxybenzene) boric acid, this product also has many other names and trade names. Its other names are: 2-fluoro-6-methoxyphenylboronic acid.
Ancient scholars have studied the name of the substance in detail. (2-fluoro-6-methoxybenzene) boric acid, in the field of chemical industry, is an important raw material. Although its names are different, they actually refer to the same thing. In various classics, it is also known as the convenience of seeking the source of reason, and the trade name is related to the easy circulation of the market. When we study this thing, we should carefully identify its name and clarify its essence, so that we can proceed unimpeded in the way of chemical research and application, just as the ancients sought knowledge and studied the changes in the name and reality, in order to achieve the realm of application.
Safety & Operational Standards
(2-Fluoro-6-methoxybenzene) boric acid is an important chemical product, which is very important for its safety and operating practices.
When preparing and handling this chemical, the first thing to pay attention to is the ventilation of the environment. Because of its volatility, good ventilation can avoid the accumulation of harmful gases and ensure the health of the operator. Furthermore, the operator must wear appropriate protective equipment, such as protective gloves, goggles and protective clothing. Protective gloves can prevent skin contact, prevent skin irritation or absorb harmful substances; goggles can protect the eyes and avoid chemical splashing; protective clothing can protect the body in all aspects.
For storage, (2-fluoro-6-methoxybenzene) boric acid should be stored in a dry, cool and ventilated place. Keep away from fire and heat sources to prevent chemical properties from changing due to temperature rise, or even cause danger. At the same time, it should be stored separately from oxidants, acids, alkalis and other substances. Because of its active chemical properties, it can mix with other chemicals or react chemically, causing safety accidents.
During use, the operation must be accurate and standardized. Take an appropriate amount of chemicals and do not exceed the required amount to avoid waste and increase danger. After operation, clean and return the equipment used, such as reactors, measuring tools, etc. Residual chemicals should be properly disposed of in accordance with relevant regulations and should not be dumped at will to prevent environmental pollution.
In short, the safety and operation specifications of (2-fluoro-6-methoxybenzene) boric acid need to be strictly controlled from the preparation, storage, use and other links to ensure personnel safety and smooth production.
Application Area
(2-Fluoro-6-methoxybenzene) boronic acid is useful in many fields. In the development of medicine, it can be used as a key intermediate to help synthesize specific drugs, which is of great benefit to the treatment of specific diseases. In the field of materials science, it can participate in the preparation of materials with specific properties, such as those with unique optical and electrical properties, or for the manufacture of advanced electronic components. In the field of organic synthesis, it is often used as an important reagent to promote various organic reactions and synthesize complex and delicate organic compounds. It is widely used, just like the stars in the vast night sky, contributing to the development of various fields, leading researchers to explore its endless potential and achieve more innovative breakthroughs.
Research & Development
Today, there is (2 - Fluoro - 6 - Methoxybenzene) Boronic Acid. Our chemical researchers have struggled with its research and development.
Initially, analyze its structure, explore its characteristics, and clarify the law of its reaction. In the process of synthesis, it has been tried and tested many times to find the best method to find a high yield.
Then, looking at its application field, thinking about medicine and materials, we can do something. Or help the production of new drugs, or benefit the properties of materials.
The process of research, although it is difficult, we will not stop. With time, we can expand its use, increase its value, add a touch of bright color to the field of chemistry, and promote the progress of this industry. This is the wish of our researchers.
Toxicity Research
The toxicity of (2-fluoro-6-methoxybenzene) boric acid is studied now. The toxicity of this substance is related to the safety of living beings and cannot be careless.
First look at its chemical properties, (2-fluoro-6-methoxybenzene) boric acid has a specific molecular structure, and the substitution of fluorine and methoxy groups may cause it to exhibit different reactivity. With this activity, it can react in the environment or with other substances to change its toxicity.
To explore its biological effects for the second time. Test it with various organisms to observe its impact on cell growth and metabolism. Observe the changes in cell morphology, measure the changes in enzyme activity, and understand its disturbance to physiological processes in organisms. And look at its characterization in animals, such as differences in behavior and organ functions, and investigate how this substance, after entering the body, follows the route, where it gathers, and how it affects the balance of the body.
In summary, a detailed study of the toxicity of (2-fluoro-6-methoxybenzene) boric acid can provide evidence for its safe use and proper disposal, and ensure ecological and human safety.
Future Prospects
In the future, it is related to (2-fluoro-6-methoxybenzene) boric acid. Although it is currently in various research, it may only emerge. Looking at the road of chemical industry, the field of organic synthesis, its potential cannot be underestimated.
In the path of pharmaceutical creation, because of its unique structure, it may be able to develop new agents, open up new paths, and help overcome difficult diseases. In the field of material innovation, it may be able to use its characteristics to breed extraordinary materials to meet the needs of future diversity.
There may be thorns in the road ahead, but with the heart of research, over time, we will be able to explore its secrets, display its brilliant brilliance, and contribute to the prosperity of chemical industry and scientific research.
Where to Buy (2-Fluoro-6-Methoxybenzene)Boronic Acid in China?
As a trusted (2-Fluoro-6-Methoxybenzene)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-6-Methoxybenzene)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-6-methoxybenzene) boronic acid
(2-Hydroxy-6-methoxybenzyl) boric acid, which has important applications in medicinal chemistry, materials science, organic synthesis and other fields.
In the field of medicinal chemistry, it is often involved in drug synthesis as a key intermediate. Gein boric acid groups have unique chemical properties, which can interact with a variety of targets in organisms, and can be used for precise chemical modification and connection when constructing complex drug molecular structures. For example, when developing new anti-cancer drugs, (2-hydroxy-6-methoxybenzyl) boric acid can participate in the formation of pharmacopharmaceuticals with specific activities, which helps to improve the targeting and efficacy of drugs on cancer cells.
In terms of material science, it can be used to prepare functional materials. Because the boric acid group can react with the surface or internal components of a specific material, thereby improving the material properties. For example, when preparing optical materials, the introduction of this boric acid compound can optimize the light absorption and emission characteristics of the material, making it suitable for optoelectronic devices. When preparing polymer materials, it can be used as a crosslinking agent or functional additive to enhance the mechanical properties and stability of the material.
In the field of organic synthesis, it is an extremely useful synthesizer. Due to the unique activity of boric acid groups in many organic reactions, such as Suzuki-Miyaura coupling reaction, (2-hydroxy- 6-methoxybenzyl) boric acid can react efficiently with substrates such as halogenated aromatics or olefins to form carbon-carbon bonds and realize the synthesis of complex organic molecules. This reaction condition is relatively mild and highly selective, and is widely used in the total synthesis of natural products and the creation of new organic functional molecules, which greatly promotes the development of organic synthesis chemistry.
What are the synthesis methods of (2-fluoro-6-methoxybenzene) boronic acid?
The synthesis of (2-hydroxy- 6-methoxybenzene) boric acid is an important topic in organic synthetic chemistry. To prepare this substance, there are several common methods.
One is to use halogenated aromatics as the starting material. First, take a benzene derivative containing a halogen atom, which can be bromine or iodine. It interacts with magnesium metal to form a Grignard reagent. Grignard reagent has high activity and can react with borate esters. After the reaction is completed, (2-hydroxy- 6-methoxybenzene) boric acid can be obtained through the hydrolysis step. In this process, the preparation of Grignard reagent needs to be carried out in an anhydrous and oxygen-free environment to prevent it from side-reacting with water and oxygen, which affects the yield and purity of the product.
Second, palladium-catalyzed coupling reaction can be used. Halogenated benzene or phenylboronic acid derivatives are used as substrates, and under the action of palladium catalyst, they are coupled with the corresponding boric acid or borate ester. This reaction condition is relatively mild and has good selectivity. However, palladium catalysts are expensive, and specific ligands are required to coordinate the reaction to promote the reaction and improve the selectivity. The choice of ligands is crucial, and different ligands have significant effects on the reaction rate, yield and selectivity.
Third, phenolic compounds are also used as starters. The phenolic hydroxyl group is properly protected first, and then the methoxy group is introduced. After that, the boric acid group is introduced by a suitable method, and the protective group is finally removed to obtain the target product. The key to this route lies in the selection of the protective group and the optimization of the removal conditions. The protective group must be stable during the reaction process and can be removed smoothly under appropriate conditions without affecting the structure of other parts of the molecule.
The above synthesis methods have their own advantages and disadvantages. In practical application, it is necessary to comprehensively consider factors such as raw material availability, cost, reaction conditions and product purity requirements to choose the most suitable method.
What are the physical properties of (2-fluoro-6-methoxybenzene) boronic acid?
(2-Hydroxy-6-methoxybenzene) boric acid is an organic compound with a wide range of uses in the field of organic synthesis. Its physical properties are as follows:
Viewed at room temperature and pressure, (2-hydroxy-6-methoxybenzene) boric acid is in the form of a white to off-white crystalline powder, which is easy to store and use, and the characteristics of the powder enable it to fully contact with other reactants during reaction, speeding up the reaction process.
Smell, the substance has no special and obvious odor, which does not cause discomfort to the environment or users due to strong odor during experimental operation and practical application.
When it comes to the melting point, the melting point of (2-hydroxy- 6-methoxybenzene) boric acid is within a certain range, and the specific value varies slightly due to factors such as purity, which is roughly within the range of melting points of common organic compounds. The existence of the melting point indicates that the transformation from solid to liquid requires specific temperature conditions. This property is of great significance in the process of separation, purification and identification, and can be used to judge its purity and material characteristics.
In terms of solubility, (2-hydroxy- 6-methoxybenzene) boric acid exhibits a certain solubility in organic solvents such as ethanol and dichloromethane, and also has slightly soluble properties in water. This solubility characteristic provides convenience for its application in different reaction systems, and suitable solvents can be selected according to the reaction requirements to make the reaction proceed smoothly.
In addition, the stability of the substance is good, and it can maintain its own chemical structure and properties for a certain period of time under conventional storage conditions. When encountering specific chemicals such as strong oxidizing agents, strong acids, and strong bases, or due to chemical reactions that change their original properties, it is necessary to avoid contact with such substances when storing and using.
What are the precautions for (2-fluoro-6-methoxybenzene) boric acid in storage and transportation?
When storing and transporting (2-hydroxy- 6-methoxybenzene) boric acid, there are a number of important precautions that need to be paid attention to.
In terms of storage, the first choice of environment. When looking for a cool, dry and well-ventilated place, this is because (2-hydroxy- 6-methoxybenzene) boric acid is prone to chemical changes in a humid and warm environment, which will damage its quality. If placed in a humid place, it may absorb moisture and deliquescence; if placed in a warm place, it may cause decomposition to accelerate. Furthermore, the storage place should be away from fire and heat sources, because it has certain chemical activity, it is dangerous to encounter open flames, hot topics or brewing. And it needs to be stored separately from oxidants, acids, alkalis, etc. Because (2-hydroxy- 6-methoxybenzene) boric acid and other such substances are prone to chemical reactions, and even cause disasters such as combustion and explosion.
As for transportation, the packaging must be tight and stable. Appropriate packaging materials need to be selected to ensure that (2-hydroxy- 6-methoxybenzene) boric acid does not leak or dissipate during transportation. Transportation vehicles should also be properly selected, clean, dry and free of residual other chemicals to prevent cross-contamination. During transportation, it is necessary to drive safely to avoid violent vibration and collision. This is due to excessive vibration, collision or package damage, which will expose (2-hydroxy- 6-methoxybenzene) boric acid and cause accidents. At the same time, transportation personnel must be familiar with relevant safety knowledge, know the characteristics of (2-hydroxy- 6-methoxybenzene) boric acid and emergency treatment methods, and in case of leakage, can be properly disposed of immediately to ensure the safety of transportation.
What is the market price and trend of (2-fluoro-6-methoxybenzene) boronic acid?
What is the market price and trend of (di-hydroxy-6-methoxynaphthalene) sulfonic acid? In the current market, the price of this drug is influenced by many factors. In terms of raw materials, if the supply of basic raw materials such as dinaphthol and methanol required for the synthesis of this sulfonic acid is sufficient and the price is stable, the cost of producing the sulfonic acid can be controlled, and the price may be relatively stable. On the contrary, if the supply of raw materials is tight due to reduced production and blocked transportation, the price will rise, which in turn will drive up the price of sulfonic acid.
From the perspective of market demand, if this sulfonic acid is in strong demand in key application fields such as medicine and dyes, such as the development of new drugs in the pharmaceutical industry, the demand for it as an intermediate increases greatly, or dye companies increase the amount of sulfonic acid due to market demand for specific color dyes, demand growth will pull up prices. And if the development of related industries is sluggish and demand is sluggish, prices will be under downward pressure.
As for the price trend, if technological progress gives birth to new synthetic processes, greatly reduce production costs, or there are substitutes with similar performance, the price of sulfonic acid may decline. If environmental protection policies become stricter, the compliance cost of manufacturers will increase, and the superimposed market demand will be stable, and the price may rise slightly.
Looking at its past market, the price of sulfonic acid fluctuated significantly due to the sharp fluctuations in the price of raw material methanol. Later, due to the expansion of new applications in the pharmaceutical field, demand increased, and prices rebounded. Now the market is gradually maturing, and in the absence of major changes in raw materials, sudden changes in demand or policy shocks, prices may remain relatively stable and adjusted slightly. But in the long run, with the technological innovation of the industry and the reshaping of the market structure, its price trend remains uncertain.