4 Bromo 2 6 Difluorobenzoic Acid
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
4-bromo-2,6-difluorobenzoic acid
Chemical Formula C7H3BrF2O2
Molar Mass 239.00
Appearance Solid
Color White to off - white
Melting Point 145 - 149 °C
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
Acidity Weakly acidic, pKa value around 3 - 4
Odor Odorless or very faint odor
Stability Stable under normal conditions, but may react with strong oxidizing agents
Name 4-bromo-2,6-difluorobenzoic acid
Molecular Formula C7H3BrF2O2
Molecular Weight 237.00
Appearance White to off - white solid
Melting Point 138 - 142 °C
Boiling Point N/A (decomposes)
Solubility In Water Slightly soluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
Pka N/A
Density N/A
Flash Point N/A
Name 4-bromo-2,6-difluorobenzoic acid
Chemical Formula C7H3BrF2O2
Molar Mass 237.00 g/mol
Appearance Solid (usually white to off - white powder)
Melting Point 145 - 147 °C
Solubility In Water Poorly soluble in water
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
Acidity Weak acid (pKa value is characteristic of benzoic acid derivatives)
Hazard May cause skin, eye and respiratory irritation
FAQ

What are the chemical properties of 4-bromo-2,6-difluorobenzoic acid

4-Bromo-2,6-difluorobenzoic acid is an organic compound. Its physical and chemical properties are unique and are of great importance in the field of organic synthesis.

Looking at its physical properties, under normal temperature and pressure, this compound is mostly in solid form. Its melting point, boiling point and other parameters are of great significance in controlling its physical state under specific conditions. Due to the fact that the molecular structure contains halogen atoms such as bromine and fluorine, the intermolecular forces are unique, which in turn affect the melting point and boiling point.

In terms of chemical properties, the carboxyl group is one of its main functional groups, so it has the chemical properties of a typical carboxylic acid. It can neutralize with bases to form corresponding carboxylate and water. If reacted with sodium hydroxide, sodium 4-bromo-2,6-difluorobenzoate can be obtained with water.

Furthermore, the halogen atom on the benzene ring also participates in many chemical reactions. Bromine atoms are highly active and can be replaced by other nucleophilic reagents through nucleophilic substitution. For example, under appropriate conditions, they can be replaced by hydroxyl groups, amino groups, etc., thereby deriving a series of new compounds. The existence of fluorine atoms, due to the high electronegativity of fluorine, can change the electron cloud density distribution of the benzene ring, affecting the activity and selectivity of the electrophilic substitution reaction on the benzene ring.

In organic synthesis, 4-bromo-2,6-difluorobenzoic acid is often used as a key intermediate. Due to its combination of carboxyl and halogen atoms, complex organic molecular structures can be constructed through various chemical reactions, which are widely used in the fields of medicine, pesticides and materials science. For example, when creating new drug molecules, their structures can be modified and modified to meet specific biological activity requirements.

What are the main uses of 4-bromo-2,6-difluorobenzoic acid

4-Bromo-2,6-difluorobenzoic acid, which has a wide range of uses. In the field of medicinal chemistry, it is often a key intermediate for the synthesis of specific drugs. Taking the development of anti-cancer drugs as an example, its unique chemical structure can be ingeniously designed and reacted to be introduced into the molecular structure of the drug, giving the drug the ability to precisely target cancer cells, and can enhance the affinity of the drug with specific targets, thereby enhancing the anti-cancer efficacy.

In the field of materials science, it also has important functions. It can be used as a starting material for the construction of special-performance polymer materials. After polymerization, its structural units are integrated into the polymer chain, thereby giving the material unique properties such as excellent thermal stability, chemical stability and optical properties. These materials have potential applications in electronic devices, optical coatings and other fields. For example, in the optical coating materials of high-end electronic display screens, the coating's anti-wear and anti-corrosion properties are improved by its special structure, and the optical transmittance is optimized.

In agricultural chemistry, 4-bromo-2,6-difluorobenzoic acid can be used to create new pesticides. It can participate in the synthesis of highly efficient, low-toxic and environmentally friendly insecticides or fungicides. By precisely acting on the specific physiological processes of pests or pathogens, good control effects are achieved, and the impact on the environment and non-target organisms is small, which helps to achieve sustainable agricultural development.

What is the synthesis method of 4-bromo-2,6-difluorobenzoic acid?

The synthesis of 4-bromo-2,6-difluorobenzoic acid is an important task in the field of organic synthesis. There are various methods, each with its own advantages and disadvantages, and the choice of method depends on the actual situation.

First, 2,6-difluorobenzoic acid can be started and the target product can be obtained by bromination reaction. In this path, brominating reagents such as liquid bromine, N-bromosuccinimide (NBS), etc. are commonly used. If liquid bromine is used, a suitable catalyst, such as iron powder or iron tribromide, should be used in a suitable reaction temperature and solvent. Using dichloromethane as a solvent and adding liquid bromine dropwise at low temperature can make the reaction occur smoothly and reduce side reactions. However, liquid bromine is highly corrosive and volatile, and the operation must be cautious.

Second, using 4-bromo-2,6-difluorotoluene as raw material, 4-bromo-2,6-difluorobenzoic acid is oxidized to obtain 4-bromo-2,6-difluorobenzoic acid. Common oxidants include potassium permanganate, potassium dichromate, etc. The potassium permanganate oxidation method is mild and easy to operate, and can be carried out in aqueous or organic-aqueous mixed systems. However, the post-reaction treatment is more cumbersome, and the resulting manganese dioxide precipitation needs to be removed.

Third, it is prepared from suitable halogenated aromatics by metal-catalyzed carboxylation. For example, palladium catalysis is used to react halogenated aromatics with carbon monoxide, bases and suitable ligands at a certain temperature and pressure. This method has high atomic economy and good selectivity, but the catalyst cost is high and the reaction conditions are strict.

To synthesize 4-bromo-2,6-difluorobenzoic acid, the appropriate synthesis path should be carefully selected after considering the factors such as raw material availability, cost, reaction conditions and product purity requirements, so as to achieve the purpose of efficient, economical and environmentally friendly synthesis.

What is the price range of 4-bromo-2,6-difluorobenzoic acid in the market?

4-Bromo-2,6-difluorobenzoic acid is on the market, and its price range is difficult to determine. The price of this compound often changes due to many factors.

First, the price of raw materials is the main factor. If the price of bromine, fluoride and other raw materials required for the preparation of this acid fluctuates due to market supply and demand, the distance of origin, and the change of seasons, the price of 4-bromo-2,6-difluorobenzoic acid also fluctuates.

Second, the simplicity of the preparation process has a great impact. If the preparation method requires exquisite equipment, harsh conditions, multiple processes, or rare catalysts, the cost will increase greatly, and its price in the market will also be high.

Third, the market supply and demand relationship is the key. If many industries have strong demand for it, such as medicine, pesticides, materials and other fields, and the supply is limited, the price will rise; conversely, if the demand is weak and the supply is full, the price will fall.

Fourth, the production scale is also related. In large-scale production, due to the scale effect, the unit cost may be reduced, and the price will also be lower; in small-scale production, the unit cost is high, and the price will be high.

Based on past market conditions, the price of this compound may range from hundreds to thousands of yuan per kilogram. However, this is only a rough estimate. To know the exact price, you need to consult chemical raw material suppliers, traders, or refer to recent market transaction records to obtain a more accurate price.

What are the storage conditions for 4-bromo-2,6-difluorobenzoic acid?

4-Bromo-2,6-difluorobenzoic acid is an organic compound, and its storage conditions are quite critical, which is related to the stability and quality of the substance. This compound should be stored in a cool, dry and well-ventilated place.

A cool environment can avoid chemical reactions or decomposition caused by high temperature. High temperature often promotes a large increase in molecular activity and causes the compound to deteriorate. Therefore, a slightly lower room temperature, such as an environment of 15-25 degrees Celsius, is more suitable.

Dry conditions are also indispensable. Because of its hygroscopicity, if it exists in a humid place, it is easy to absorb water, which affects the purity and chemical properties. In a dry environment, it can prevent reactions such as hydrolysis caused by moisture intervention.

Good ventilation is also crucial. If stored in a closed, airless place, volatile gases will accumulate, or increase the risk of explosion, poisoning, etc. And ventilation can keep the environment dry and help prevent moisture.

Furthermore, 4-bromo-2,6-difluorobenzoic acid should be stored separately from oxidants, bases and other substances. Because of its acidic nature, it is easy to neutralize when in contact with bases; while oxidants are strong oxidizing, coexisting with them or causing violent reactions, endangering safety.

When storing, make sure that the container is well sealed. To prevent the compound from coming into contact with air and causing oxidation and other reactions. It is also important to choose the right storage container, which should be corrosion-resistant, such as glass or specific plastic containers, to avoid the reaction between the container and the compound and ensure the purity and stability of the material.