4 Cyano 1 2 Difluorobenzene
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
4-CYANO-1,2-DIFLUOROBENZENE
Chemical Formula C7H3F2N
Molecular Weight 139.10
Appearance Colorless to light yellow liquid
Boiling Point 190 - 192 °C
Melting Point N/A
Density 1.287 g/cm³
Solubility Slightly soluble in water, soluble in organic solvents
Flash Point 72 °C
Refractive Index 1.495 - 1.497
Purity Typically high purity available, e.g., 98%+
Chemical Formula C7H3F2N
Appearance Colorless to light yellow liquid
Boiling Point 183 - 185 °C
Density 1.27 g/cm³
Flash Point 69 °C
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
Stability Stable under normal conditions
Chemical Formula C7H3F2N
Molar Mass 139.102 g/mol
Appearance Liquid (usually)
Boiling Point Approximately 184 - 186 °C
Density Data varies, typically in range of 1.2 - 1.3 g/cm³
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Vapor Pressure Low at room temperature
FAQ

What is the main use of 4-CYANO-1,2-DIFLUOROBENZENE?

4-Cyano-1,2-difluorobenzene has a wide range of uses. In the field of organic synthesis, its position is pivotal. This compound is often a key starting material for the construction of complex organic molecules.

First, in pharmaceutical chemistry, it can be used as an important intermediate for the synthesis of new drugs. Many drug molecules with specific biological activities often involve structural modification and expansion based on this. The special electronic effects and spatial structure of cyano and difluorophenyl groups endow subsequent synthetic products with unique pharmacological properties, which may enhance the affinity between drugs and targets, or improve the metabolic stability of drugs, thus providing the possibility for the creation of new drugs with high efficiency and low toxicity.

Second, in the field of materials science, 4-cyano-1,2-difluorobenzene also has outstanding performance. It can be used to prepare functional materials with excellent performance, such as organic optoelectronic materials. Due to its molecular structure properties, it may exhibit good photoelectric conversion properties in optoelectronic devices, such as in organic Light Emitting Diode (OLED), organic solar cells and other fields, which is expected to improve the efficiency and stability of the device.

Furthermore, in the field of pesticide chemistry, this raw material can be used to synthesize pesticides with high insecticidal, bactericidal or herbicidal activities. The introduction of cyano and fluorine atoms can significantly enhance the effect of pesticide molecules on target organisms, and the special properties of fluorine atoms can enhance the environmental adaptability and residue characteristics of pesticides, making pesticides more in line with the requirements of modern green agriculture for high efficiency, low toxicity and low residue.

Therefore, 4-cyano-1,2-difluorobenzene plays an indispensable role in many fields such as organic synthesis, medicine, materials and pesticides, and is a widely used and crucial organic compound.

What are the physical properties of 4-CYANO-1,2-DIFLUOROBENZENE?

4-Cyano-1,2-difluorobenzene is one of the organic compounds. Its physical properties are quite unique, let me tell you one by one.

First of all, its appearance, at room temperature, 4-cyano-1,2-difluorobenzene is mostly colorless to light yellow liquid, clear and has a special appearance. Its color and shape are the first characteristics of identifying this substance.

Secondary and melting point and boiling point. The melting point is related to the transition temperature between the solid and liquid states of the substance. The melting point of 4-cyano-1,2-difluorobenzene is low, which makes it difficult for the substance to solidify at room temperature, and it usually remains liquid. As for the boiling point, its boiling point is moderate. When the external temperature rises to a certain level, the substance will transform from liquid to gaseous state. This boiling point value is of great significance for the separation and purification of substances.

Furthermore, when it comes to density. Its density is different from that of water, and this difference has a great impact on the distribution and behavior of substances in the liquid phase system. If mixed with water, its density characteristics can clearly show its floating or sinking situation in water, which helps the experimenter to judge and operate.

Solubility is also an important physical property. 4-Cyano-1,2-difluorobenzene exhibits good solubility in organic solvents, such as certain aromatics, halogenated hydrocarbons, etc., and can be miscible with it to form a uniform solution. However, in water, its solubility is very small, due to the difference between its molecular structure and the polarity of water.

In addition, 4-cyano-1,2-difluorobenzene also has a certain degree of volatility, which will slowly disperse into the air in an open environment. This volatility also affects its storage and use. It needs to be properly sealed and stored to prevent material loss and possible safety hazards.

And its unique smell, although it is difficult to describe accurately, but the smell can sense its special smell, this smell can also be used as the basis for preliminary identification.

In summary, the physical properties of 4-cyano-1,2-difluorobenzene are diverse, and the application in chemical industry, scientific research and other fields requires detailed knowledge of its various properties in order to achieve the purpose of safe and efficient use.

What are the chemical properties of 4-CYANO-1,2-DIFLUOROBENZENE?

4-Cyano-1,2-difluorobenzene is one of the organic compounds. It has unique chemical properties and has a wide range of uses in the field of organic synthesis.

In this compound, the cyano group (-CN) is connected to the difluorobenzene ring. The cyano group is active and can often participate in many chemical reactions. In nucleophilic substitution reactions, the cyano group can be used as a nucleophilic reagent to react with suitable substrates to form carbon-carbon bonds, which is crucial in the construction of complex organic molecular structures.

Furthermore, the two fluorine atoms on the benzene ring have an impact on the electron cloud distribution and spatial structure of the compound. Fluorine atoms have strong electronegativity, which can reduce the electron cloud density of the benzene ring, which in turn affects the electrophilic substitution reaction activity on the benzene ring. Compared with unfluorinated benzene derivatives, the electrophilic substitution reaction of 4-cyano-1,2-difluorobenzene has different check points and reactivity. Usually, the presence of fluorine atoms makes the electrophilic substitution reaction more likely to occur at a specific location, due to the combined effect of the induction effect of fluorine atoms and the conjugation effect.

In terms of stability, the presence of cyanyl and fluorine atoms makes the molecule stable to a certain extent. The carbon-nitrogen triple bond in the cyanyl group is quite high, and the carbon-fluorine bond between the fluorine atom and the benzene ring is also relatively strong. However, under certain conditions, such as high temperature, strong acid and base or the presence of specific catalysts, its structure can still change.

In terms of solubility, because of its polar cyanyl group and non-polar benzene ring structure, it has a certain solubility in organic solvents. It can be soluble in common organic solvents such as dichloromethane and tetrahydrofuran, but its solubility in water is relatively low, which is due to the hydrophobicity of the molecule as a whole.

The chemical properties of 4-cyano-1,2-difluorobenzene make it an important synthetic intermediate in the fields of medicine, pesticides and materials science. It can prepare many compounds with specific functions and properties through various reactions.

What are the synthesis methods of 4-CYANO-1,2-DIFLUOROBENZENE?

There are several common methods for the synthesis of 4-cyano-1,2-difluorobenzene.

First, it is obtained by cyanylation with 1,2-difluorobenzene as the starting material. Suitable cyanidation reagents, such as cuprous cyanide, can be selected. Under suitable reaction conditions, such as in a specific solvent, heating and stirring are used to promote the cyanyl group to replace the hydrogen atom on the benzene ring to form the target product. This method is relatively direct and the raw material is relatively easy to obtain.

Second, it is synthesized by molecular rearrangement or substitution of other compounds containing cyanide groups and fluorine atoms. For example, some fluorine-containing nitrile compounds, under the action of specific catalysts, undergo intramolecular rearrangement, so that the position of the cyano group and the fluorine atom conforms to the structural requirements of 4-cyano-1,2-difluorobenzene. This approach requires precise control of the reaction conditions to ensure that the reaction proceeds in the desired direction.

Third, it is prepared by cyanylation of halogenated aromatics. First, the benzene ring is introduced into the halogen atom, such as chlorine atom or bromine atom, to obtain 1-halo-2-fluorobenzene, and then the cyanide reagent reacts with it. The halogen atom is replaced by a cyano group, and finally 4-cyano-1,2-difluorobenzene is obtained In this process, the activity of halogen atoms has a great influence on the reaction, and suitable halogenated aromatics and reaction conditions need to be selected to improve the reaction yield.

Each synthesis method has its own advantages and disadvantages, and the most suitable synthesis route should be selected after comprehensive consideration according to the actual situation, such as the cost of raw materials, the difficulty of reaction, and the purity requirements of the product.

What are the precautions for 4-CYANO-1,2-DIFLUOROBENZENE in storage and transportation?

4-Cyano-1,2-difluorobenzene is an important compound in organic chemistry. During storage and transportation, many points must be observed.

First word storage. This compound is more active and needs to be placed in a cool, dry and well-ventilated place. Due to the characteristics of cyano and fluorine atoms, it is easy to chemically react when wet, so moisture avoidance is the most important. If the environment is humid, or the compound is deteriorated, it will lose its original chemical properties, which will affect subsequent use. And it must be kept away from fire and heat sources, because it is flammable to a certain extent, under high temperature or open flame, there is a risk of fire.

Furthermore, the storage place should be separated from oxidants, acids, bases, etc. The chemical structure of 4-cyano-1,2-difluorobenzene makes it prone to severe chemical reactions or serious consequences such as explosion when it encounters the above substances.

As for transportation, there are also many precautions. Transportation vehicles must ensure that they are in good condition and have corresponding fire and explosion-proof devices. When loading, they should be placed firmly to avoid collisions and vibrations to prevent package damage and compound leakage. During transportation, drivers and escorts should always pay attention and not leave their posts without authorization. In case of emergencies such as leakage, they should be dealt with quickly according to the established emergency plan. < Br >
During transportation and storage, relevant personnel must be familiar with the characteristics and emergency treatment methods of 4-cyano-1,2-difluorobenzene. In this way, the safety of storage and transportation can be guaranteed, and accidents can be avoided.