P Cyanofluorobenzene
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
p-Cyanofluorobenzene
Name p-Cyanofluorobenzene
Chemical Formula C7H4FN
Molar Mass 121.11 g/mol
Appearance Colorless liquid
Boiling Point 186 - 187 °C
Melting Point -17 °C
Density 1.12 g/cm³
Solubility In Water Insoluble
Flash Point 68 °C
Refractive Index 1.508 (20 °C)
Odor Faintly aromatic
Name p-Cyanofluorobenzene
Chemical Formula C7H4FN
Molar Mass 121.11 g/mol
Appearance Colorless to pale yellow liquid
Boiling Point 185 - 186 °C
Melting Point -27 °C
Density 1.106 g/cm³
Solubility In Water Insoluble
Flash Point 68 °C
Refractive Index 1.5145
Vapor Pressure 1.33 hPa (44.6 °C)
Chemical Formula C7H4F N
Molecular Weight 121.11
Appearance Colorless liquid
Odor Characteristic
Density 1.13 g/cm³ at 25 °C
Boiling Point 187 - 188 °C
Melting Point −10.5 °C
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents
Flash Point 71 °C
Vapor Pressure 0.13 kPa at 25 °C
Refractive Index 1.5225 at 20 °C
FAQ

What are the main uses of p-Cyanofluorobenzene?

P-Cyanofluorobenzene is p-cyanofluorobenzene. Its main uses are as follows:

p-cyanofluorobenzene is used in the field of organic synthesis. First, it is often used to create various drugs. In medicinal chemistry, it can be used as a key intermediate to prepare compounds with specific biological activities. For example, some drug molecules with antibacterial, anti-inflammatory or anti-tumor activities may be synthesized by p-cyanofluorobenzene. Through a series of chemical reactions, other functional groups are introduced into the molecular structure, and finally the desired drug molecule is constructed. This is because both cyano and fluorine atoms have significant effects on the biological activity and physicochemical properties of molecules. The presence of cyano groups can enhance the polarity of molecules, which in turn affects their interaction with biological targets; fluorine atoms can change the properties of fat solubility and metabolic stability of compounds, making it easier for drugs to penetrate biofilms and prolong the action time in the body.

Second, in materials science, p-cyanofluorobenzene also has applications. It can be used to prepare functional polymer materials. By introducing p-cyanofluorobenzene into the polymer skeleton, the material can be imparted with unique electrical, optical or thermal properties. For example, when preparing liquid crystal materials, the special structure of p-cyanofluorobenzene can make the prepared liquid crystal have specific phase transition temperature and orientation characteristics, which has potential applications in the field of display technology. Due to its regular molecular structure, it helps to arrange molecules in an orderly manner and promote the formation of liquid crystal phases, so as to achieve effective control of the direction of light propagation and meet the needs of liquid crystal displays and other devices.

Furthermore, in the field of pesticide synthesis, p-cyanofluorobenzene is also an important raw material. It can be used to synthesize a variety of high-efficiency and low-toxicity pesticides. By rationally designing the reaction route, it can be converted into pesticide ingredients with insecticidal, bactericidal or herbicidal activities. For example, using its structural characteristics to synthesize pesticides with specific effects on specific pests or pathogens, improve the targeting of pesticides, and reduce the impact on non-target organisms, which is in line with the development trend of modern green pesticides.

What are the physical properties of p-Cyanofluorobenzene?

P-Cyanofluorobenzene is p-cyanofluorobenzene. Its physical properties are as follows:

p-cyanofluorobenzene is an organic compound. It is mostly colorless to light yellow liquid at room temperature and pressure, and has a clear appearance. This substance has a specific odor, but the description of the relevant odor is not exhaustive.

Its molecular weight is 121.11, the melting point is around -20 ° C, and the boiling point is about 189-190 ° C. The density of this substance is about 1.13 g/cm ³, which is slightly higher than that of water, so it will sink in water.

p-cyanofluorobenzene is slightly soluble in water, but it can be well miscible with most organic solvents, such as ethanol, ether, acetone, etc. This solubility characteristic is due to the fact that its molecular structure contains both hydrophobic benzene rings and polar cyanobenzene and fluorine atoms, which makes it easier to disperse in organic solvents.

In addition, the vapor pressure of p-cyanobenzene fluoride is relatively low at room temperature, and the volatility is not very significant. However, in a heated or open environment, its vapor can still escape slowly. Because it has both fluorine atoms and cyanobenzene groups, it is chemically active and can participate in many organic reactions, making it widely used in the field of organic synthesis.

What is the chemistry of p-Cyanofluorobenzene?

For p-Cyanofluorobenzene, there are also compounds. The fluorine atom in its molecule is cyanyl, which gives its specialization.

In terms of its chemical properties, the cyanyl group has the property of absorbers, which can reduce the density of benzene, making it easier to generate substitution and reverse, and the substitution positions are mostly at the position of the cyanyl group (that is, the position where the fluorine atom is located). Due to the absorber effect of the cyanyl group, the sub-cloud on the benzene group is biased towards the cyanyl group, so that the density of the sub-cloud at the low-position and the low-position is reduced, and the low-position phase is enriched. Therefore, the low-position is more attractive.

The fluorine atom is also a absorber, but due to the p-π co-effect, the density of the benzene sub-cloud can increase, and the reactivity can be affected to a certain extent. The coexistence of the two results in p-Cyanofluorobenzene.

Cyanyl groups can generate multiple reactions, such as hydrolysis under acid or catalysis to form amides and carboxylic acids. It can also be used to form new carbon-carbon atoms and expand molecules.

Fluorine atoms can make molecules have certain lipid properties, and carbon-fluorine atoms can improve the chemical quality of compounds. It can also be replaced by nuclear reagents. Under suitable conditions, fluorine atoms can be implanted by other nuclear reagents, introducing new functionalities, and deriving polymers, which are useful in the field of synthesis.

What are the preparation methods of p-Cyanofluorobenzene?

P-cyanofluorobenzene, an organic compound also. The method of its preparation, as described in the past literature, has about the following numbers.

First, p-fluorobenzoic acid is used as the starting material, so that it is co-heated with urea, and can be prepared by dehydration reaction. This reaction needs to be carried out at a suitable temperature and in the presence of a catalyst. P-fluorobenzoic acid and urea are mixed in a certain proportion, placed in a reactor, and heated to a specific temperature. Catalysts such as certain metal oxides or salts can accelerate the reaction process. In the reaction, the carboxyl group of benzoic acid and the amino group of urea undergo dehydration and condensation, and gradually generate p-cyanofluorobenzene.

Second, p-fluorobenzene is used as the raw material and can be obtained by cyan First, p-fluorobrobenzene reacts with metal cyanides, such as cuprous cyanide, in an appropriate organic solvent at a certain temperature and pressure. The bromine atom of p-fluorobrobenzene is replaced by a cyanyl group, and the choice of organic solvent is very critical. It is necessary to be able to dissolve the reactants without interfering with the reaction. The control of this reaction condition is extremely important. Excessive temperature or improper pressure may cause side reactions to occur, affecting the purity and yield of the product.

Third, using p-nitrofluorobenzene as the starting material, p-aminofluorobenzene is first obtained by reduction reaction, and then it is diazotized, and then reacted with reagents such as cuprous cyanide to convert it into p-cyanofluorobenzene. Suitable reducing agents such as iron powder and hydrochloric acid are commonly used in reduction The diazotization reaction needs to be carried out under low temperature and specific acidic conditions to ensure the stability of the diazonium salt. Subsequent reactions with cuprous cyanide also need to precisely control the reaction conditions to efficiently prepare p-cyanofluorobenzene.

What are the precautions in storage and transportation of p-Cyanofluorobenzene?

P-cyanofluorobenzene, chemical substances are also. During storage and transportation, many matters must not be ignored.

First word storage. This material is a chemical agent and needs to be stored in a cool, dry and well-ventilated place. Avoid open flames and hot topics to prevent it from reacting due to heat and causing danger. Because of its certain chemical activity, it should be stored separately from oxidants, acids, alkalis and other substances, and must not be stored in combination to avoid chemical reactions and endanger safety. At the same time, the storage place should be equipped with corresponding varieties and quantities of fire equipment and leakage emergency treatment equipment to prevent accidents.

Times and transportation. When transporting, it is necessary to ensure that the container does not leak, collapse, fall or damage. The transport vehicle should be equipped with corresponding fire equipment and leakage emergency treatment equipment. During driving, it should be protected from exposure to the sun, rain and high temperature. Road transportation needs to follow the specified route, do not stop in residential areas and densely populated areas. During transportation, the escort must always pay attention to the status of the goods, and if any abnormalities are detected, they should be disposed of quickly and properly.

All of these are the key to the storage and transportation of p-cyanofluorobenzene. Practitioners should follow them carefully to ensure safety.