Chemical Formula | C8H4F3N |
Molecular Weight | 171.12 |
Appearance | Colorless to light yellow liquid |
Boiling Point | 188 - 190 °C |
Density | 1.28 g/cm³ |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents |
Flash Point | 73 °C |
Refractive Index | 1.448 - 1.450 |
Stability | Stable under normal conditions |
Chemical Formula | C8H4F3N |
Molar Mass | 171.12 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | 203 - 204 °C |
Melting Point | N/A |
Density | 1.299 g/cm³ |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents |
Flash Point | 86 °C |
Purity | Typically high purity in commercial products |
What are the main uses of 2,3,6-trifluorobenzyl cyanide?
2% 2C3% 2C6-trifluorobenzyl ether has a wide range of main uses. In the field of organic synthesis, this compound is often a key intermediate. Because its structure contains special trifluoromethyl and benzyl ether groups, it is endowed with unique chemical properties, so it can participate in a variety of chemical reactions and assist chemists in constructing complex organic molecular structures.
For example, in pharmaceutical chemistry, this material can be used as a raw material to synthesize compounds with specific pharmacological activities through a series of reactions. Because of its strong electron absorption, trifluoromethyl can adjust the fat solubility, metabolic stability and interaction with drug molecules, thereby improving the efficacy and selectivity of drugs. In many new drug development paths, 2% 2C3% 2C6-trifluorobenzyl ether is often used as a starting material or an important intermediate, helping to create new drugs with high efficiency and low toxicity.
In the field of materials science, it also has outstanding performance. It can be used as a key component in the synthesis of functional materials, and it can be introduced into polymers or other material systems through chemical reactions to improve the properties of materials. Such as enhancing the chemical resistance, thermal stability and surface characteristics of materials. With the characteristics of trifluoromethyl, the surface of the material can form an interface with low surface energy, which has potential application value in waterproof, oil-proof, anti-fouling and other fields.
Furthermore, in the preparation of fine chemical products, 2% 2C3% 2C6-trifluorobenzyl ether can be used to synthesize special fragrances, dyes and additives. Because of its unique physical and chemical properties, it can meet the special needs of fine chemicals in different industries.
What are the physical properties of 2,3,6-trifluorobenzyl cyanide?
2% 2C3% 2C6-tribromobenzyl bromide is also an organic compound. Its physical properties are quite unique, let me tell them one by one.
Looking at its morphology, under room temperature and pressure, 2% 2C3% 2C6-tribromobenzyl bromide is often in a solid state, which is due to its intermolecular force. Its texture is relatively solid, but it is not indestructible.
As for the color, it is mostly white to light yellow. The cause of this color is related to factors such as electron transitions in the molecular structure. Its appearance is simple and not gorgeous, but it contains unique value in the field of chemistry.
When it comes to odor, 2% 2C3% 2C6-tribromobenzyl bromide has a certain pungent odor. This odor is due to the chemical properties of its molecules, and it is slightly uncomfortable to smell. Therefore, when handling this substance, it is necessary to take precautions to avoid hurting the sense of smell.
In addition to its solubility, in organic solvents, such as common ether, dichloromethane, etc., 2% 2C3% 2C6-tribromobenzyl bromide exhibits good solubility. This property allows it to fully contact and mix with many reactants during the reaction process of organic synthesis, promoting the smooth progress of the reaction. However, in water, its solubility is very small, because its molecular polarity is quite different from that of water molecules.
When it comes to melting point, the melting point of 2% 2C3% 2C6-tribromobenzyl bromide is within a certain range, and this melting point value is of great significance for experimental operations such as separation, purification and identification. Accurate determination of melting point can determine the purity and authenticity of this substance.
In addition, its density is also an important physical property. Compared with water, 2% 2C3% 2C6-tribromobenzyl bromide has a higher density. If it is placed in the same container as water, it will sink to the bottom. This property can be used in some experiments or industrial production processes involving liquid-liquid separation.
All these physical properties are interrelated and together constitute the unique physical characterization of 2% 2C3% 2C6 -tribromobenzyl bromide, which lays the foundation for its research and application in the field of chemistry.
What are the chemical properties of 2,3,6-trifluorobenzyl cyanide?
2% 2C3% 2C6-tribromophenyl ether is a kind of organic compound. Its properties are also flame retardant, and it is often used as a flame retardant in various materials to prevent fire.
This substance is chemically stable, temperature-resistant and resistant to degradation. Its molecule contains bromine atoms. Bromine can generate hydrogen halide when burned, which coats on the surface of the combustion substance, isolates oxygen and suppresses the chain reaction of combustion, and has a flame retardant effect.
However, it also has drawbacks. It is difficult to degrade in the environment, easy to accumulate, and gradually becomes an environmental pollutant. It enters the organism, or interferes with endocrine, affecting physiological processes such as reproduction and development of organisms. In the past, many people used it as a flame retardant, but it was gradually regulated due to the hidden dangers of the environment and health.
Although its flame retardant contribution is indispensable, it is necessary to weigh the pros and cons and find better alternatives to ensure the safety of the environment and biology.
What are the synthesis methods of 2,3,6-trifluorobenzyl cyanide?
The synthesis of 2% 2C3% 2C6-trifluorobenzyl ether covers a variety of methods. One method is also to use halogenated benzyl and trifluoroalcohol as raw materials, supplemented by alkali, under suitable reaction conditions, nucleophilic substitution reaction is carried out. The halogen atom of the halogenated benzyl is active, and when it encounters a base, it will lead to the nucleophilic attack of the oxygen anion of trifluoroalcohol to form an ether bond to obtain the target product. If benzyl bromide and trifluoroethanol are used as the starting point, potassium carbonate is used as the base, and the reaction can be carried out smoothly in an organic solvent such as acetonitrile. The product can be separated and purified to obtain a pure 2% 2C3% 2C6-trifluorobenzyl ether. < Br >
Another method uses benzyl alcohol derivatives and trifluorohalogenated hydrocarbons as raw materials. The benzyl alcohol hydroxyl group is properly activated, such as converted into a sulfonate group, and then reacts with the trifluorohalogenated hydrocarbons under the action of metal catalysts or bases. Metal catalysts such as copper salts and palladium salts can promote the formation of carbon-oxygen bonds. If benzyl p-toluenesulfonate is reacted with trifluoroiodomethane and cesium carbonate is used as a base, it can also be prepared by heating the reaction in N, N-dimethylformamide solvent. After the reaction, the product can be obtained by means of extraction, column chromatography, etc.
Furthermore, the phase transfer catalysis method is used. Using benzyl halide and trifluoroalcohol as basic raw materials, a phase transfer catalyst, such as quaternary ammonium salts, is added to the water-organic two-phase system. The phase transfer catalyst can transfer the nucleophile in the aqueous phase to the organic phase, so that the reaction can be carried out efficiently. At a suitable temperature and stirring rate, the product can be obtained after reacting for a period of time, and then the product can be purified by regular separation steps.
What are the precautions for 2,3,6-trifluorobenzyl cyanide in storage and transportation?
For 2% 2C3% 2C6-tribromobenzylane, various precautions are very important during storage and transportation. This substance has certain particularities and needs to be handled with caution.
When storing, the temperature and humidity of the environment are the first priority. It should be placed in a cool, dry place to avoid high temperature and humidity. If it is in a high temperature environment, it may cause its properties to change, and even cause danger. Due to high temperature, it can accelerate the rate of chemical reactions, or cause decomposition and deterioration. Humid gas is also a taboo, which may react with moisture, affect the quality, and moisture is easy to breed microorganisms such as mold, contaminating this substance.
Furthermore, the storage place must be well ventilated. This is to disperse the harmful gases that may be generated, avoid their accumulation, and cause safety hazards. And ventilation can maintain fresh ambient air and reduce the adverse effects on the substance itself.
During transportation, the packaging must be sturdy and tight. To prevent vibration and collision from causing damage to the package and causing material leakage. Select suitable packaging materials, which must be able to withstand certain external shocks and have good sealing properties.
Transportation tools should also be clean and free of residues that react with 2% 2C3% 2C6-tribromobenzylane. And during transportation, escorts should pay close attention to the transportation conditions to ensure that the temperature, humidity and other conditions meet the requirements. If there is any abnormality, take immediate measures.
Also, whether it is storage or transportation, it must be kept away from fire, heat and strong oxidizing agents. This substance may be flammable or can react violently with oxidizing agents, causing serious accidents such as fire and explosion. Therefore, fireworks are strictly prohibited around storage and transportation vehicles, and dangerous items such as oxidizing agents are placed and transported separately to ensure safety.