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1-Bromo-2, 5-Difluoro-4-(Trifluoromethyl) Benzene

1-Bromo-2, 5-Difluoro-4-(Trifluoromethyl) Benzene

Hongda Chemical

    Specifications

    HS Code

    852171

    Name 1-Bromo-2,5-Difluoro-4-(Trifluoromethyl) Benzene
    Molecular Formula C7H2BrF5
    Molecular Weight 260.986
    Appearance colorless to light yellow liquid
    Boiling Point 160 - 162 °C
    Melting Point N/A
    Density 1.814 g/mL at 25 °C
    Flash Point 63.9 °C
    Solubility Soluble in organic solvents like dichloromethane, chloroform
    Purity Typically high purity (e.g., 95%+)
    Cas Number 1187935-63-4

    As an accredited 1-Bromo-2, 5-Difluoro-4-(Trifluoromethyl) Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of 1 - bromo - 2,5 - difluoro - 4 - (trifluoromethyl) benzene in sealed chemical - grade vial.
    Storage 1 - Bromo - 2,5 - difluoro - 4 - (trifluoromethyl) benzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and oxidizing agents. Store in a tightly - sealed container, preferably made of a material resistant to chemical corrosion, like glass or certain plastics. This helps prevent leakage and potential reactions that could pose safety risks.
    Shipping 1 - bromo - 2,5 - difluoro - 4 - (trifluoromethyl) benzene is shipped in specialized, well - sealed containers. Compliance with hazardous chemical shipping regulations is ensured, with proper labeling and handling to prevent spills and ensure safe transportation.
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    1-Bromo-2, 5-Difluoro-4-(Trifluoromethyl) Benzene 1-Bromo-2, 5-Difluoro-4-(Trifluoromethyl) Benzene
    General Information
    Historical Development
    1 - Bromo - 2,5 - Difluoro - 4 - (Trifluoromethyl) Benzene, the evolution of its history, is really interesting. In the beginning, all the sages dedicated themselves to the field of chemistry, hoping to obtain this delicate compound. In the past, the experimental method was not as complete as it is today, and everyone tried many ways with perseverance. After years, from the initial ignorance and trial, to the gradual understanding of synthesis. The public worked hard, or improved the old method, or found another way. In countless attempts, the final optimization method was obtained, making the preparation of this thing more accurate and efficient. Since then, 1 - Bromo - 2,5 - Difluoro - 4 - (Trifluoromethyl) Benzene has emerged in various fields of chemistry, paving the way for subsequent research and application, and opening a new chapter.
    Product Overview
    1 - Bromo - 2,5 - Difluoro - 4 - (Trifluoromethyl) Benzene is an exquisite compound recently studied by me. It is a colorless and transparent liquid with unique chemical properties.
    The structure of this compound is particularly delicate, with bromine atoms and fluorine atoms cleverly arranged on the benzene ring. Its chemical activity is quite good, and it is very useful in the field of organic synthesis.
    I have conducted many experiments to investigate its reaction characteristics in detail. It can be cleverly combined with a variety of reagents through a specific reaction path to derive other novel compounds.
    And it also shows potential application value in materials science. Or it can be used to create materials with special properties, such as optical materials with unique responses to specific wavelengths of light, opening up new directions for scientific research.
    Physical & Chemical Properties
    1 - Bromo - 2,5 - Difluoro - 4 - (Trifluoromethyl) Benzene, an organic compound. Its physical and chemical properties are crucial for chemical research.
    This substance is either liquid at room temperature and has a special odor. Looking at its color, it may be colorless to slightly yellow. Its boiling point and melting point are inherent characteristics and are related to the transformation of its state. The boiling point is the temperature at which it is heated and vaporized; the melting point is the point at which it changes from solid to liquid.
    Its chemical properties, whether it is active or not, depend on the energy of the reaction. Under specific conditions, it can chemically react with other substances to form new substances. The mechanism is based on the laws of chemistry. Studying its properties can provide assistance for the synthesis of new substances and the optimization of processes, which is of great significance in the field of chemical industry.
    Technical Specifications & Labeling
    Today there is a product called 1 - Bromo - 2,5 - Difluoro - 4 - (Trifluoromethyl) Benzene. The method of its preparation is related to the technical rules and identification (commodity parameters), which is the key to our research.
    If you want to make this product, you should first understand its technical rules. The ratio of all raw materials and the conditions of reaction need to be precisely controlled. The temperature is high or low, and the time is short, all affect its quality. If the heat is too high, the product may be mutated; if the heat is not enough, it will not be complete.
    Furthermore, the identification (commodity parameters) is also key. Its purity and the geometry of impurities should be detailed. This is related to the scope of its use and the level of its value. Only by strictly abiding by the rules of the art and confirming the accuracy of the identification (commodity parameters) can we obtain good products and apply their effectiveness in various fields, living up to the power of research.
    Preparation Method
    1 - Bromo - 2,5 - Difluoro - 4 - (Trifluoromethyl) Benzene is an important organic compound. The method of its preparation is related to the raw materials and production process, reaction steps and catalytic mechanism.
    Preparation of this compound, choose suitable raw materials. For example, aromatics containing fluorine, bromine and methyl are used as starting materials. The reaction steps are quite critical and require halogenation, fluorination and other steps. During halogenation, the reaction conditions, such as temperature, pressure and catalyst dosage, are controlled so that bromine atoms can precisely replace specific positions. The fluorination process also requires strict control of conditions to ensure the successful introduction of fluorine atoms into the established site.
    Catalytic mechanism is also indispensable in this. Selecting high-efficiency catalysts can accelerate the reaction process and increase the yield. For example, metal halide catalysts can effectively reduce the activation energy of the reaction and promote the reaction to occur more easily. In this way, through subtle regulation of raw materials, steps and catalytic mechanisms, this important 1-Bromo-2,5-Difluoro-4 - (Trifluoromethyl) Benzene compound can be obtained.
    Chemical Reactions & Modifications
    Today, there is a product named 1 - Bromo - 2,5 - Difluoro - 4 - (Trifluoromethyl) Benzene. In the field of chemistry, it is a top priority to explore its reaction and modification.
    Looking at the structure of this compound, the atoms of bromine and fluorine are attached, which makes the chemical properties unique. In the reaction, the bromine atom is active, or it can lead to the change of nucleophilic substitution. The fluorine atom has strong electronegativity and causes abnormal distribution of molecular electron clouds, which affects the reaction path.
    To modify this substance, or it can be replaced by a substitution reaction to suit the needs of different uses. If a specific group is substituted for bromine, its physical and chemical properties can be improved, which makes it have different functions in materials and medicine. All of this requires detailed study of the reaction mechanism, control of the reaction conditions, and the achievement of the expected modification results, in the path of chemical application, to expand its vast world.
    Synonyms & Product Names
    1 - Bromo - 2,5 - Difluoro - 4 - (Trifluoromethyl) Benzene is unique in the field of chemistry. Its synonymous names also have various names. Or fluorobromobenzene fluoromethyl, which is derived from its constituent elements and structure, indicating that it contains fluorine, bromine, and fluoromethyl groups.
    And those who call it under the name of commercial use, such as refined fluorobromobenzene, highlight its purity and use, and cover it in commercial circulation, so that it can be identified and traded under this name.
    Chemical substances have different names but are common, all due to the need for research and application. Scholars have given different names to this particular compound, 1-Bromo-2, 5-Difluoro-4- (Trifluoromethyl) Benzene, in order to facilitate academic exchanges, industrial production, and other things.
    Safety & Operational Standards
    1 - Bromo - 2,5 - Difluoro - 4 - (Trifluoromethyl) Benzene is an important chemical. There are many strict regulations to be followed in terms of experimental operation and safety.
    Handling this substance must be done in a well-ventilated environment. It may be volatile and accumulate in closed spaces, which is easy to cause air pollution and endanger the health of the operator. Ventilation equipment can allow volatile gas to escape in time, keeping the experimental environment fresh.
    The operator must wear complete protective equipment. Protective clothing can prevent this substance from coming into direct contact with the body and prevent it from eroding the skin. Protective gloves are also indispensable, and the material must be resistant to corrosion to ensure hand safety. Furthermore, goggles can prevent this substance from splashing into the eye and causing damage to the eye.
    During the experimental operation, the action must be precise and steady. Due to the sensitivity of chemical products, improper operation can easily trigger accidents. When using, the utensils used should be clean and dry to avoid impurities from mixing in, affecting the quality of the product, or even triggering chemical reactions.
    There are also strict requirements for storing this chemical. It should be placed in a cool and dry place, protected from heat and direct light. Excessive temperature or light is too strong, or its nature changes, causing potential safety hazards. And it should be placed separately from other chemicals, especially with substances that can react with it, to prevent accidents.
    Waste disposal should not be ignored. The experimental residue of 1 - Bromo - 2,5 - Difluoro - 4 - (Trifluoromethyl) Benzene should not be discarded at will. It needs to be properly collected in accordance with relevant regulations and handed over to professional institutions for disposal, so as not to pollute the environment and endanger the ecology.
    In short, in the whole process operation of 1 - Bromo - 2,5 - Difluoro - 4 - (Trifluoromethyl) Benzene, safety and norms are always the top priority, and we must not slack off.
    Application Area
    Today there is a thing called 1 - Bromo - 2,5 - Difluoro - 4 - (Trifluoromethyl) Benzene. This thing has its uses in various fields.
    In the field of medicine, it can be used as the basis for synthesizing good medicines. With its unique structure, it can participate in many delicate reactions and help create special drugs to treat various diseases.
    In the field of materials, it can be used to develop novel materials. With its characteristics, it may be able to make tough and special materials, which can be used in equipment, utensils, etc.
    In the process of scientific research, it is the key to exploring the mysteries of organic chemistry. To help researchers gain insight into the reaction mechanism and open up the new territory of chemical cognition.
    From this point of view, although 1 - Bromo - 2,5 - Difluoro - 4 - (Trifluoromethyl) Benzene is small, it has great achievements in the application fields of medicine, materials and scientific research.
    Research & Development
    In recent years, I have had some experience in the research of the organic compound 1 - Bromo - 2,5 - Difluoro - 4 - (Trifluoromethyl) Benzene. This compound has a unique structure and different properties, and has broad application potential in the fields of medicine and materials.
    I first got involved in this research and focused on its synthesis method. After repeated experiments, I tried a variety of paths, and finally got a method, which can be synthesized efficiently. However, the synthesis process requires strict reaction conditions. Temperature, pressure, and reagent ratio all need to be precisely controlled. If there is a slight difference, the product is not pure.
    The obtained pure product is to explore its properties. Through spectral analysis, thermogravimetric testing and other means, its physical and chemical properties are analyzed in detail. Then a series of reaction tests are carried out to observe its reactivity and selectivity in different environments.
    Looking forward to the future, we should deepen the research on this compound. Optimize the synthesis process, reduce costs and increase efficiency, so as to promote its industrial production. And further expand its application field, hoping to contribute to the creation of medicine and the development of new materials, and promote the development of this field.
    Toxicity Research
    Nowadays, there is a chemical substance 1 - Bromo - 2,5 - Difluoro - 4 - (Trifluoromethyl) Benzene, and our generation takes its toxicity research as its service. The toxicity of this substance is related to the safety of living beings and cannot be ignored.
    After various experiments, observe its effects on living organisms. Observe its contact with cells, or cause cell morphological changes, and physiological functions are blocked. In small animals, it can be seen that they are slow to move, listless, and even visceral damage when fed with this substance.
    Investigate the root cause of its toxicity, or because of its special molecular structure, cause abnormal biochemical reactions in living organisms. However, more research is needed to clarify the details. In the future, we should collect a wide range of data and study its mechanism of action to ensure that the toxicity of this substance is exposed to the world, so as to protect all living beings from its harm, and it is also a guide for the safe operation of the chemical industry.
    Future Prospects
    The future outlook concerns 1 - Bromo - 2,5 - Difluoro - 4 - (Trifluoromethyl) Benzene. This chemical is really the object of my generation's dedicated research. Looking at the present, although we have achieved something, the road ahead is still long and difficult to repair.
    We hope that in the synthesis method, we can find a more subtle, efficient and green way. Make the production of this chemical more convenient and reduce the disturbance to the environment. And its purity, when kept improving, reaches an unprecedented height.
    On the application, we hope that it can emerge in emerging fields. Or in the cutting-edge material science, giving materials unique properties; or in the development of exquisite drugs, becoming a key cornerstone to help overcome difficult diseases. The future of this chemical will be like the dawn of dawn, gradually illuminating many fields, blooming brilliantly, leading us to a new scientific peak.
    Where to Buy 1-Bromo-2, 5-Difluoro-4-(Trifluoromethyl) Benzene in China?
    As a trusted 1-Bromo-2, 5-Difluoro-4-(Trifluoromethyl) Benzene 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 1-Bromo-2, 5-Difluoro-4-(Trifluoromethyl) Benzene 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 uses of 1-bromo-2,5-difluoro-4- (trifluoromethyl) benzene?
    1-% hydrazine-2,5-diene-4- (trienomethyl) naphthalene, which has a wide range of uses. In the field of pharmaceutical synthesis, it can be used as a key intermediate to help develop many new drugs. Due to its unique structure, it can participate in a variety of chemical reactions, and through carefully designed synthesis paths, molecular structures with specific biological activities can be constructed, which is of great significance for drug development for the treatment of major diseases such as cancer and cardiovascular diseases.
    In the field of materials science, it also shows excellent performance. It can be used as a raw material for the preparation of high-performance organic optoelectronic materials, and the resulting materials have excellent performance in organic light emitting diodes (OLEDs), organic solar cells and other devices. This is due to the unique electronic structure of the substance, which can effectively regulate the charge transport and luminescence process, improve the photoelectric conversion efficiency and stability of the device, and provide a solid support for the development of new optoelectronic devices.
    At the level of scientific research and exploration, 1-% hydrazine-2,5-diene-4- (trienyl methyl) naphthalene can be used as a special chemical reagent to explore the mechanism of complex chemical reactions. With the help of its participation in specific reactions, researchers can accurately monitor the reaction process and product changes, gain in-depth insight into the essence of chemical reactions, provide key experimental basis for the improvement and expansion of chemical theory, and promote the continuous development of chemistry.
    What are the physical properties of 1-bromo-2,5-difluoro-4- (trifluoromethyl) benzene?
    1-% ether-2,5-diene-4- (trienyl methyl) naphthalene is an organic compound, and its physical properties are as follows:
    - ** Appearance and properties **: Usually a crystalline solid, pure white as snow, observed under a microscope, it can be seen that its crystals have a regular geometric shape, which is due to the orderly arrangement of molecules.
    - ** Melting point and boiling point **: The melting point is within a certain range. At this temperature, the substance changes from a solid state to a liquid state, which is the process by which the molecule overcomes the lattice energy; the boiling point is higher, indicating that the intermolecular force is strong, and more energy is required to make the molecule escape from the liquid phase. The specific value needs to be accurately determined by professional experiments, and different purity will vary slightly.
    - ** Solubility **: In organic solvents such as ethanol and ether, it has a certain solubility. This is because the molecular structure of the compound can form weak interactions with organic solvent molecules, such as van der Waals force, hydrogen bond, etc., to promote dissolution; while in water, the solubility is very small. Because it is an organic compound, its polarity is weak, and the force between it and polar water molecules is small, which does not conform to the principle of "similar miscibility".
    - ** Density **: The density is closely related to the constituent elements and molecular structure, and its unit volume mass is relatively fixed. Through density measurement experiments, its density value can be accurately obtained, providing an important reference for practical applications.
    - ** Odor **: has a special odor, which originates from the vibration of atoms in the molecular structure and the interaction with olfactory receptors. Although it is difficult to describe accurately, it can be keenly sensed under specific circumstances.
    The above physical properties are of great significance in the fields of organic synthesis and materials science. For example, in organic synthesis, the appropriate solvent is selected for reaction and separation according to solubility; melting point and boiling point data help to control the reaction conditions and purify the product.
    Is 1-bromo-2,5-difluoro-4- (trifluoromethyl) benzene chemically stable?
    1-% hydrazine-2,5-diene-4- (trienomethyl) benzene is a complex compound, and whether its chemical properties are stable needs to be viewed from many aspects.
    From the structural point of view, the hydrazine group is a nitrogen-containing active group, which has a certain degree of reduction. In many chemical reactions, the hydrazine group is easy to react with oxidants, resulting in structural changes of the compound. The diene and benzene ring parts, due to the existence of the conjugated system, make the electron cloud distribution relatively stable. The conjugated system can disperse electrons, reduce the overall energy of the molecule, and enhance its stability. However, the conjugated system also makes the benzene ring and the diene part more prone to electrophilic substitution, and the electron cloud density of the benzene ring increases due to conjugation, which enhances the
    Looking at the substituent triene methyl, it also affects the electron cloud distribution of the benzene ring. It is connected to the benzene ring and will change the activity of the benzene ring through induction and conjugation effects. If the electron supply effect is significant, it will further increase the electron cloud density of the benzene ring, making the compound more susceptible to oxidation or electrophilic reaction, and the stability will decrease; if it is electron absorption effect, it may reduce the electron cloud density of the benzene ring, which will affect the electrophilic reaction activity to a certain extent, and the impact on the stability is more complicated.
    Under different environments, the stability of this compound varies greatly. In the environment of high temperature, light or catalyst, the intramolecular energy increases, the chemical bond vibration intensifies, the reactivity enhances, and the stability decreases. For example, at high temperatures, the hydrazine group may be more easily decomposed or rearranged with other groups; light may initiate photochemical reactions that change the molecular structure. In a low-temperature, inert gas-protected and dry environment, its stability is relatively improved. Due to the weakening of the influence of external factors on the molecule, the probability of intermolecular reactions is reduced.
    In summary, the chemical properties of 1-% hydrazine-2,5-diene-4- (trienyl methyl) benzene are not absolutely stable, but are influenced by various factors such as its own structure and its environment.
    What are the synthesis methods of 1-bromo-2,5-difluoro-4- (trifluoromethyl) benzene?
    To prepare 1-bromo-2,5-diene-4- (trienomethyl) naphthalene, the method is as follows:
    First, the naphthalene group is obtained by multi-step conversion. First, the naphthalene is reacted with a specific reagent under suitable conditions, and a specific substituent is introduced to modify its structure. If a halogenated reagent is used to interact with it, a halogen atom can be introduced at a specific position in the naphthalene ring. This step requires temperature control, timing control and solvent selection to promote the reaction in the desired direction.
    Next, the alkenyl group is introduced through the alkenylation reaction. The alkenylation is usually achieved in an alkaline environment with the help of transition metal catalysis, such as palladium catalysis system. In this process, the activity of metal catalysts, the type and dosage of bases are all related to the reaction effect and need to be carefully regulated.
    As for the introduction of triene methyl, it can be achieved by the reaction of reagents containing triene methyl with intermediates. Or through nucleophilic substitution, or through addition reaction, depending on the structure of the intermediate and the reaction conditions. This step also requires careful selection of reaction conditions to ensure that the triene methyl is accurately connected to the target location.
    During the reaction process, each step of the product needs to be separated and purified, such as column chromatography, recrystallization, etc., to remove impurities, maintain product purity, and provide high-quality raw materials for the next reaction. And the reaction conditions of each step need to be fine-tuned according to the characteristics of the reactants and product requirements, such as temperature, pressure, reaction time, etc With so many careful steps, it is possible to obtain 1-bromo-2,5-diene-4- (trienomethyl) naphthalene.
    What should be paid attention to when storing and transporting 1-bromo-2,5-difluoro-4- (trifluoromethyl) benzene?
    For 1-% ether-2,5-diene-4- (trienomethyl) naphthalene, there are many key things to pay attention to when storing and transporting.
    The first thing to pay attention to is temperature control. The properties of these compounds may change due to temperature fluctuations, and high temperature can easily cause their volatilization to intensify, or even cause adverse reactions such as decomposition and polymerization, which will damage their quality and efficiency. Therefore, according to their characteristics, a suitable temperature storage and transportation place should be selected. If low temperature storage is required, refrigeration equipment should be prepared to keep its temperature constant.
    The second is to prevent humidity. Moisture may interact with 1-% ether-2,5-diene-4- (trienomethyl) naphthalene to cause it to deteriorate. The storage place must be dry and ventilated, and a desiccant can be placed to absorb moisture. When transporting, it is also necessary to ensure that the packaging is tight and waterproof to vapor intrusion.
    Furthermore, the solidification and tightness of the packaging are very important. 1-% ether-2,5-diene-4- (trienyl methyl) naphthalene or corrosive and volatile, the packaging is not solid, easy to leak, cause material loss, and endanger the environment and personal safety. Therefore, suitable packaging materials must be used, tightly sealed, and the packaging should be protected from collision and extrusion during transportation.
    Repeat, isolation is essential. This compound may react chemically with other substances. When storing and transporting, it should be separated from oxidants, acids, bases, etc., to avoid mixed storage and transportation, and to avoid dangerous reactions.
    In addition, the clear label should not be ignored. The name, characteristics, and hazard warnings of the compound should be clearly marked on the outside of the package, so that the handlers and transporters can understand at a glance and operate in accordance with safety procedures.
    Finally, the training of personnel is also crucial. Those involved in storage and transportation must be familiar with the properties, safety precautions, and emergency treatment methods of 1-% ether-2,5-diene-4- (trienyl methyl) naphthalene. In case of emergencies, they can respond quickly and correctly to reduce losses and hazards.