Chemical Formula | C7H4FNO |
Molar Mass | 137.11 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | 204 - 205 °C |
Melting Point | −12 °C |
Density | 1.194 g/cm³ |
Solubility In Water | Insoluble |
Flash Point | 84 °C |
Refractive Index | 1.527 |
Vapor Pressure | Low at room temperature |
Chemical Formula | C7H4FNO |
Molar Mass | 137.11 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | 203 - 205 °C |
Melting Point | 16 - 18 °C |
Density | 1.229 g/cm³ |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether |
Flash Point | 82 °C |
Refractive Index | 1.529 - 1.531 |
Vapor Pressure | Low vapor pressure at room temperature |
Chemical Formula | C7H4FNO |
Molecular Weight | 137.11 |
Appearance | Colorless to light yellow liquid |
Boiling Point | 201 - 202 °C |
Melting Point | -26 °C |
Density | 1.196 g/cm³ |
Flash Point | 83 °C |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents |
Vapor Pressure | Low vapor pressure |
What are the main uses of m-Cyanofluorobenzene?
M-Cyanofluorobenzene (m-Cyanofluorobenzene) is a crucial intermediate in the field of organic synthesis, and is widely used in various industries such as medicine, pesticides, and materials.
In the pharmaceutical industry, it can be used as a key intermediate to synthesize a variety of drug molecules with specific biological activities. Both the cyanyl group and the fluorine atom can have a significant impact on the physicochemical properties and biological activities of drug molecules. The introduction of fluorine atoms can enhance the lipid solubility of drug molecules, promote their transmembrane transportation, and improve bioavailability; cyanyl groups can participate in a variety of biochemical reactions, enhance the interaction between drugs and targets, and then improve drug efficacy. For example, when developing new anti-tumor drugs, m-cyanofluorobenzene can undergo a series of reactions to build a structure that is closely bound to the target of tumor cells, achieving the purpose of inhibiting the growth and proliferation of tumor cells.
In the field of pesticides, m-cyanofluorobenzene also plays an important role. With it as a starting material, pesticides with high insecticidal, bactericidal or herbicidal activities can be synthesized. The presence of fluorine atoms and cyanobenzyl groups can enhance the toxicity and selectivity of pesticide molecules to target organisms, reduce the impact on non-target organisms, and meet the needs of modern green pesticide development. For example, the synthesis of new insecticides can precisely act on the specific physiological processes of pests, effectively kill pests, and reduce the harm to the environment and beneficial organisms.
In the field of materials science, m-cyanofluorobenzene can be used to prepare functional materials with excellent performance. If it is introduced into the main chain or side chain of the polymer as a structural unit when synthesizing high-performance polymer materials, it can endow the material with unique electrical, optical or thermal properties. Polymers containing cyanide groups and fluorine atoms may have good heat resistance, chemical stability and electrical insulation, and have great application potential in electronic devices, aerospace and other fields.
With its unique chemical structure, m-cyanofluorobenzene has shown indispensable value in many important industries and plays a key role in promoting technological progress and innovation in various fields.
What are the physical properties of m-Cyanofluorobenzene?
M-cyanofluorobenzene, its physical properties are as follows:
This substance is mostly liquid at room temperature, and it is clear and transparent. Its boiling point is between about 180-190 ° C. At this temperature, the liquid absorbs enough heat, and the thermal motion of the molecules intensifies, so it changes from liquid to gaseous. The melting point is roughly -20 ° C. When the temperature drops to this point and below, the molecular activity is limited, and the substance solidifies from liquid to solid.
M-cyanofluorobenzene has a slightly higher density than water, about 1.18-1.22 g/cm ³, so if mixed with water, it will sink underwater. It is insoluble in water, because of its molecular structure, the presence of cyanyl (-CN) and fluorine atoms (-F) makes the molecular polarity different from water molecules. According to the principle of similar miscibility, the two are difficult to dissolve with each other. However, in organic solvents, such as ethanol, ethyl ether, dichloromethane, etc., it has good solubility, because the force between the molecules of the organic solvent and the organic solvent can cause them to mix with each other.
In addition, m-cyanofluorobenzene is volatile, will slowly evaporate in the air, and has certain toxicity due to the cyanide group. When using and storing, it is necessary to pay attention to sealed storage and operate in a well-ventilated place to avoid harm to the human body and the environment. Its odor is special, although it is difficult to describe accurately, it is irritating, and people can clearly perceive it when they smell it.
What is the chemistry of m-Cyanofluorobenzene?
M-cyanofluorobenzene is also an organic compound. Its molecule contains a cyano group (CN) and a fluorine atom (F), which has unique chemical properties.
In terms of its activity, the cyano group is a strong electron-withdrawing group, and the fluorine atom also has an electron-withdrawing effect. The synergistic effect of the two results in a decrease in the electron cloud density of the benzene ring. This characteristic decreases the activity of the electrophilic substitution reaction of the benzene ring, and it is more difficult to occur electrophilic substitution than benzene.
In terms of nucleophilic substitution reactions, the cyanyl group can participate in many nucleophilic reactions. In case of nucleophilic reagents, the carbon and nitrogen tri Due to the electron-withdrawing properties of the cyanyl group, the electron cloud density of the adjacent and para-position of the benzene ring connected to it decreases, and the adjacent and para-position are more vulnerable to nucleophilic reagents.
Although fluorine atoms are highly electronegative, due to their small atomic radius, the C-F bond energy formed with carbon is large. Under normal conditions, the C-F bond is relatively stable and not easy to break. However, under certain strong nucleophilic reagents and suitable reaction conditions, fluorine atoms can be replaced by nucleophilic reagents, and fluorine atoms can be replaced by other groups.
In addition, m-cyanobenzene fluorobenzene can also participate in metal-catalyzed reactions. For example, under the catalysis of transition metals, cyanyl groups can participate in coupling reactions to build more complex organic molecular structures. This compound is often used as a key intermediate in the field of organic synthesis to prepare biologically active drug molecules, functional materials, etc. Its special chemical properties provide organic synthesis chemists with a variety of reaction pathways and strategies to achieve efficient construction of target compounds.
What are m-Cyanofluorobenzene synthesis methods?
M-cyanofluorobenzene is an important intermediate in organic synthesis. There are several ways to synthesize it.
First, m-fluorobenzoic acid is used as the starting material. M-fluorobenzoic acid is heated with thionyl chloride to obtain m-fluorobenzoyl chloride. This reaction requires attention to the control of the reaction temperature to prevent side reactions from happening. M-fluorobenzoyl chloride reacts with ammonia to obtain m-fluorobenzamide first. This step requires the selection of a suitable solvent to facilitate the reaction. M-cyanobenzene can be obtained by treating m-fluorobenzene with a dehydrating agent such as phosphorus pentoxide.
Second, m-fluorobenzene is used as the starting material. M-fluorobromobenzene reacts with cuprous cyanide in a suitable solvent and temperature. This reaction requires the assistance of ligands to promote the substitution of cyano groups. This is a nucleophilic substitution reaction. M-cyanofluorobenzene can be obtained. However, cuprous cyanide is highly toxic, and caution and comprehensive protection must be taken during operation.
Third, m-fluoroaniline is used as the starting material. M-fluoroaniline first reacts with sodium nitrite and hydrochloric acid to form a diazonium salt. This diazonium salt reacts with a mixture of cuprous cyanide and potassium cyanide to obtain m-cyanofluorobenzene. This reaction also needs to pay attention to the control of reaction conditions. The diazonium salt is unstable, and the operation should be fast to prevent its decomposition.
Each of the above methods has its own advantages and disadvantages. In actual synthesis, it should be selected according to factors such as the availability of raw materials, cost, and difficulty of reaction conditions.
m-Cyanofluorobenzene What are the precautions during storage and transportation?
M-cyanofluorobenzene is also a chemical substance. During storage and transportation, many matters must not be ignored.
The first word is storage. First, choose a cool, dry and well-ventilated place. Because the substance is prone to change when heated, its properties are unstable, so it is important to avoid heat. If placed in a hot place, or cause the substance to deteriorate, its quality will be damaged. Second, it must be stored separately from oxidizing agents, acids, bases, etc. This is because of its chemical activity. When encountering such substances, it may react violently and cause the risk of explosion. Third, the storage place should be prepared with suitable containment materials. If there is a leak, it can be quickly contained to prevent it from spreading and causing greater harm.
Second talk about transportation. When transporting, the packaging must be tight. Choose the packaging material suitable for this object to ensure that it is not damaged by vibration or collision during transportation. When handling, workers should be careful and handle it lightly. To prevent damage to the packaging and leakage of substances. The transportation vehicle also needs to be clean, dry, and free of other chemical substances to avoid mixing and reaction. At the same time, the transporter should be familiar with the dangerous characteristics of the substance and the emergency treatment methods. In case of emergencies, it can be responded to in time to reduce the damage.
All these are the attention of the storage and transportation of m-cyanobenzene fluorobenzene. All things are cautious, and the security is complete, so as to avoid any accidents.