1 Bromo 4 Fluorobenzene
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
1-bromo-4-fluorobenzene
Chemical Formula C6H4BrF
Molar Mass 175.00 g/mol
Appearance Colorless to light yellow liquid
Boiling Point 150 - 152 °C
Melting Point -28 °C
Density 1.579 g/mL at 25 °C
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
Flash Point 48 °C
Refractive Index 1.5335 - 1.5355 (20 °C)
Chemical Formula C6H4BrF
Molecular Weight 175.00
Appearance Colorless to light yellow liquid
Boiling Point 150 - 153 °C
Melting Point -32 °C
Density 1.57 g/cm³
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
Flash Point 46 °C
Refractive Index 1.533 - 1.535
Vapor Pressure 1.33 kPa (39.4 °C)
Chemical Formula C6H4BrF
Molar Mass 175.00 g/mol
Appearance Colorless to light yellow liquid
Density 1.57 g/cm³ (at 25 °C)
Boiling Point 154 - 156 °C
Melting Point -27 °C
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
Flash Point 49 °C
Refractive Index 1.525 (at 20 °C)
Odor Characteristic aromatic odor
Name 1 - bromo - 4 - fluorobenzene
Molecular Formula C6H4BrF
Molar Mass 175.00 g/mol
Appearance Colorless to pale yellow liquid
Density 1.574 g/mL at 25 °C
Boiling Point 154 - 156 °C
Melting Point -27 °C
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in many organic solvents like ethanol, ether
Flash Point 49 °C
Odor Aromatic odor
FAQ

What is the main use of 1 - bromo - 4 - fluorobenzene

1-Bromo-4-fluorobenzene is also an organic compound. It has a wide range of uses and is important in the fields of chemical industry and medicine.

In the chemical industry, 1-bromo-4-fluorobenzene is a key organic synthesis intermediate. It can react with different reagents through various chemical reactions to construct various complex organic molecular structures. For example, through nucleophilic substitution reactions, its bromine or fluorine atoms can be replaced by other functional groups to prepare organic compounds with specific properties and structures, such as new polymer monomers, functional materials, etc., to help develop novel functional materials in the field of materials science and improve the special properties of materials, such as electrical conductivity and optical properties.

In the field of medicine, 1-bromo-4-fluorobenzene also has a significant effect. The synthesis of many drugs depends on it as a starting material. Because the bromine and fluorine atoms on the benzene ring can participate in the design and construction of drug molecules, affecting the activity, selectivity and pharmacokinetic properties of drugs. Based on it, drug molecules with specific pharmacological activities can be synthesized through multi-step reactions, such as antibacterial, anti-inflammatory, anti-tumor and other drugs, which can help the treatment of diseases and the progress of pharmaceutical research and development.

Furthermore, in the study of organic synthetic chemistry, 1-bromo-4-fluorobenzene is also a commonly used model compound. Through the study of its reactivity and reaction mechanism, researchers can deeply explore the laws and characteristics of organic chemical reactions, provide theoretical basis and practical experience for the development and optimization of new synthetic methods, and promote the development of organic synthetic chemistry. In short, 1-bromo-4-fluorobenzene plays an indispensable role in the fields of chemical industry, medicine and scientific research, and makes great contributions to the progress and development of related industries.

What are the physical properties of 1 - bromo - 4 - fluorobenzene

1-Bromo-4-fluorobenzene is also an organic compound. It has unique physical properties, let me tell you one by one.

First of all, its appearance, at room temperature, 1-bromo-4-fluorobenzene is colorless to light yellow liquid, clear and has a special smell. Looking at it, you can feel its clear state.

When it comes to boiling point, the boiling point of this compound is about 154 ° C. The boiling point is the critical temperature at which a substance changes from liquid to gaseous state. At this temperature, the molecule of 1-bromo-4-fluorobenzene obtains enough energy to break free from the liquid phase and turn into a gaseous state. The value of its boiling point is a key parameter in chemical operations such as separation and purification.

In terms of melting point, the melting point of 1-bromo-4-fluorobenzene is about -27 ° C. The melting point is the temperature limit for solid to liquid state. Below this temperature, it is in a solid state, and above it is in a liquid state. The characteristics of the melting point are of great significance in the control of storage, transportation and related reaction conditions.

Furthermore, the density of 1-bromo-4-fluorobenzene is about 1.57 g/cm ³. The density is also the mass per unit volume of the substance. This value indicates that its density is higher than that of water. If mixed with water, it will sink underwater. This property can be used as an important basis for processes involving liquid-liquid separation.

Solubility is also an important physical property. 1-Bromo-4-fluorobenzene is slightly soluble in water, but soluble in many organic solvents, such as ethanol, ether, acetone, etc. This difference in solubility is due to the characteristics of its molecular structure, which is different from the interaction between water molecules and organic solvent molecules. In the field of organic synthesis, its solubility characteristics determine the choice of reaction solvent, which is related to the process and efficiency of the reaction.

In summary, the physical properties of 1-bromo-4-fluorobenzene, such as appearance, boiling point, melting point, density, and solubility, each have their own uses, and are indispensable factors for chemical industry, scientific research, and many other aspects.

Chemical properties of 1 - bromo - 4 - fluorobenzene

The chemical properties of 1-bromo-4-fluorobenzene are worthy of in-depth investigation. In this compound, both bromine and fluorine are halogen elements, each of which has unique properties and has a great impact on the overall properties of the molecule.

As far as the nucleophilic substitution reaction is concerned, due to the strong electronegativity of fluorine, the electron cloud density of the benzene ring decreases, making it easier for nucleophiles to attack. At the same time, the fluorocarbon bond energy is quite high, and the substitution reaction requires more severe conditions. In contrast, the bromine-carbon bond is easier to break, so the bromine atom is more likely to be replaced by nucleophilic reagents. If encountering nucleophilic reagents such as hydroxyl negative ions, the bromine atom may be replaced by

In the electrophilic substitution reaction, although the halogen atom is an ortho-and para-localization group, the electron cloud density of the benzene ring decreases due to the electron-absorbing induction effect, so that the electrophilic substitution reaction activity is lower than that of benzene. Although both bromine and fluorine have localization effects, fluorine has strong electronegativity, and its para-localization ability may be more significant. In case of nitrification, nitro groups or more are introduced into the para-site of fluorine atoms.

In addition, 1-bromo-4-fluorobenzene can participate in the coupling reaction of metal catalysis. In the presence of suitable metal catalysts and ligands, its bromine atoms can be coupled with carbon-containing nucleophiles to form carbon-carbon bonds, which are widely used in the field of organic synthesis and can be used to prepare complex organic molecules.

Because of its halogen-containing atoms, under specific conditions, it may undergo elimination reactions to dehalide hydrogen and generate products containing unsaturated bonds. And because of its aromatic ring structure, it has certain stability and can withstand many reaction conditions, providing a convenient basis for organic synthesis.

What are the synthesis methods of 1 - bromo - 4 - fluorobenzene

1-Bromo-4-fluorobenzene is an important intermediate in organic synthesis. The synthesis method has the following numbers.

First, benzene is used as the starting material. First, benzene is brominated to obtain bromobenzene. The bromination process often involves bromine and benzene, catalyzed by iron powder or iron tribromide, slowly reacting. In this reaction, bromine atoms replace hydrogen atoms on the benzene ring to obtain bromobenzene. Then, bromobenzene and fluoride undergo a nucleophilic substitution reaction. In general, potassium fluoride can be used to heat the reaction in the presence of an appropriate solvent and catalyst, so that the fluorine atom replaces the position of the bromine atom in bromobenzene, and then 1-bromo-4-fluorobenzene is obtained.

Second, p-bromoaniline is used as the raw material. First, p-bromoaniline is reacted by diazotization, and the amino group is converted into a diazonium salt at low temperature with reagents such as sodium nitrite and hydrochloric acid. Later, fluoroboric acid is added to convert the diazonium salt into a fluoroborate salt. This salt is heated and decomposed, and nitrogen is released. At the same time, p-bromofluorobenzene is formed, which is 1-bromo-4-fluorobenzene.
< b First, p-fluorobenzoic acid is reduced to obtain p-fluorobenzyl alcohol. Then p-fluorobenzyl alcohol reacts with brominating agents, such as phosphorus tribromide, and the hydroxyl group is replaced by bromine atoms to synthesize 1-bromo-4-fluorobenzene.

These synthesis methods have their own advantages and disadvantages. It is necessary to choose carefully according to the specific experimental conditions, the availability of raw materials and costs, etc., in order to achieve the best synthetic effect.

Precautions for 1 - bromo - 4 - fluorobenzene during storage and transportation

1 + -Bromo-4 -fluorobenzene is an organic compound. When storing and transporting, many matters need to be paid attention to.

First, storage, because it has a certain chemical activity, should be stored in a cool and ventilated warehouse. If the temperature of the warehouse is too high, it may cause changes in its chemical properties, or even cause danger. Keep away from fire and heat sources. Open flames and hot topics can easily trigger reactions. It should be stored separately from oxidants, edible chemicals, etc., and must not be mixed to prevent interaction and adverse consequences. The warehouse should also be equipped with suitable materials to contain leaks. If there is a leak, it can be dealt with in time to prevent its spread from causing greater harm.

As for transportation, this compound must be carried out in accordance with the rules for the transportation of hazardous chemicals. The transportation vehicle should ensure that the vehicle is in good condition and has corresponding safety facilities and protective equipment. During transportation, the driver and the escort must pay close attention to avoid violent vibration and collision of the vehicle to prevent material leakage due to damaged packaging. Summer transportation should be selected in the morning and evening to avoid high temperature and hot sun, because it is sensitive to temperature, high temperature or increased risk. When loading and unloading, the operation must also be cautious, light loading and unloading, so as not to damage the container. And the transportation personnel should be familiar with the characteristics of this compound and emergency treatment methods. In case of leakage and other accidents, they can respond quickly and correctly to reduce the damage hazard.