Chemical Formula | C7H3BrF3 |
Molecular Weight | 241.00 |
Appearance | Liquid (usually) |
Boiling Point | Around 170 - 172 °C |
Density | Typically around 1.7 - 1.8 g/cm³ |
Solubility | Soluble in organic solvents like dichloromethane, ethyl acetate |
Flash Point | Caution: Flammable, flash point data may vary but likely in flammable range |
Refractive Index | nD ~1.47 (approximate value) |
Purity | Commercially available in various purities, often 95%+ |
What are the main uses of alpha-Bromo-2,4,6-trifluorotoluene?
Alpha-bromo-2,4,6-trifluorotoluene, this substance has a wide range of uses. In the field of organic synthesis, it is often used as a key intermediate. Due to its high activity of bromine atoms in the molecule, it can participate in many chemical reactions, such as nucleophilic substitution reactions. With this reaction, various functional groups can be introduced to construct complex organic molecular structures.
In the field of medicinal chemistry, its role cannot be ignored. In the process of many drug development, the unique physical, chemical and biological activities of fluorinated organic compounds are required. α-Bromo-2,4,6-trifluorotoluene, as a fluorine-containing compound with active bromine atoms, can be converted into a substance with specific pharmacological activities through a series of reactions, and is expected to become a potential pharmaceutical ingredient for the treatment of various diseases.
In the field of materials science, its uses have also been demonstrated. For example, it can be used to prepare fluoropolymer materials. By introducing it into polymerization reactions, the material is endowed with special properties such as excellent weather resistance, chemical stability and low surface energy. Such materials are widely used in coatings, plastics and other industries, which can significantly improve the quality and performance of materials.
In addition, in the field of pesticide chemistry, α-bromo-2,4,6-trifluorotoluene can also play an important role. After appropriate chemical modification, pesticide compounds with high insecticidal, bactericidal or herbicidal activities can be synthesized to assist in the control of pests and diseases and the removal of weeds in agricultural production, so as to ensure the yield and quality of crops.
What are the physical properties of alpha-Bromo-2,4,6-trifluorotoluene?
Alpha-bromo-2,4,6-trifluorotoluene is one of the organic compounds. Its physical properties are particularly important, and if you look at it in detail, there are the following numbers.
First of all, its appearance is usually colorless to light yellow liquid, clear and with a specific luster, which is visible to the naked eye. Its smell is irritating, and its unique smell can be sensed. When manipulating this substance, this smell is often characteristic of initial perception.
When it comes to boiling point, it is about a certain temperature range. Due to the intermolecular forces, its boiling point can be determined, which is very critical in operations such as separation and purification. The value of the boiling point makes it possible to realize the transition from liquid to gaseous state under specific temperature conditions, thus distinguishing it from other substances.
Melting point is also an important physical property. At the corresponding low temperature, α-bromo-2,4,6-trifluorotoluene will solidify from liquid to solid state. The specific value of this melting point reflects the change of its molecular arrangement and interaction at low temperature, which is of great significance for the setting of storage and transportation conditions.
Furthermore, density is also a key consideration. Its density is specific, and it is lighter or heavier than common substances such as water. This property is related to its distribution in the solution system, and has a significant impact on many chemical reactions and experimental operations.
In terms of solubility, in organic solvents, α-bromo-2,4,6-trifluorotoluene often exhibits good solubility and can be miscible with organic solvents such as ether and chloroform. However, its solubility in water is quite limited, which is determined by the matching relationship between its molecular polarity and solvent polarity.
In summary, the physical properties of α-bromo-2,4,6-trifluorotoluene, such as appearance, odor, boiling point, melting point, density and solubility, are interrelated and meaningful, and are indispensable factors in many fields such as organic synthesis and chemical analysis.
What are the chemical properties of alpha-Bromo-2,4,6-trifluorotoluene?
Alpha-Bromo-2,4,6-trifluorotoluene is an organic compound with unique chemical properties. Its chemical activity is quite high, due to the presence of bromine atoms. Bromine atoms are highly active and easily participate in many chemical reactions, such as nucleophilic substitution reactions.
In nucleophilic substitution reactions, due to the difference in electronegativity of bromine atoms, the electron cloud distribution between bromine atoms and connected carbon atoms is uneven. The bromine atoms are slightly positively charged and easily attacked by nucleophilic reagents. Nucleophilic reagents provide electron pairs and bond with the positively charged carbon atoms in alpha-Bromo-2,4,6-trifluorotoluene, while bromine atoms leave in the form of bromine ions.
Because there are three fluorine atoms connected to the benzene ring, the fluorine atom is extremely electronegative, which can absorb electrons, resulting in a decrease in the electron cloud density of the benzene ring. This structural feature not only affects the reactivity of the benzene ring itself, but also has an effect on the reactivity of the bromine atom at the alpha position. On the one hand, the electron cloud density of the benzene ring decreases, making it difficult for the electrophilic substitution reaction to occur; on the other hand, the electron-withdrawing effect of the fluorine atom enhances the positive electricity of the carbon atom at the alpha position, making the bromine atom more likely to leave, thereby enhancing the activity of alpha-Bromo-2,4,6-trifluorotoluene in the nucleophilic substitution reaction.
In addition, alpha-Bromo-2,4,6-trifluorotoluene may participate in In such reactions, the bromine atom of alpha-Bromo-2,4,6-trifluorotoluene can form intermediates with metal catalysts, and then couple with other organic reagents to construct more complex organic molecular structures.
The chemical properties of alpha-Bromo-2,4,6-trifluorotoluene are rich, and it has broad application prospects in the field of organic synthesis. With its unique structure and reactivity, it can prepare a variety of organic compounds.
What are the synthesis methods of alpha-Bromo-2,4,6-trifluorotoluene
To prepare α-bromo-2,4,6-trifluorotoluene, 2,4,6-trifluorotoluene is often used as the starting material and obtained by bromination reaction. The method is as follows:
Place 2,4,6-trifluorotoluene in a reactor, add an appropriate amount of initiator, such as benzoyl peroxide. Warm up to an appropriate temperature, usually in the range of 100-150 ° C, and slowly pass bromine. This reaction process needs to be closely monitored. Because bromine is active, the reaction is easy to overdo. When bromine is introduced, the rate should be slow to make the reaction sufficient and smooth.
After the reaction is completed, cool the reaction mixture and extract the product with an appropriate amount of organic solvent such as dichloromethane. The extraction solution is washed with a dilute alkali solution such as sodium bicarbonate to remove unreacted bromine and acidic impurities. Then it is washed with distilled water until neutral, and anhydrous sodium sulfate is dried.
Then, by distillation under reduced pressure, the organic solvent is removed, and the corresponding boiling point fraction is collected to obtain α-bromo-2,4,6-trifluorotoluene.
In addition, there are also those who use 2,4,6-trifluorobenzyl alcohol as a raw material. It is first reacted with hydrobromic acid or brominated reagents such as phosphorus tribromide, and the hydroxyl group is replaced by bromine to obtain the target product. In this way, the reaction conditions are relatively mild, and no high temperature and special initiator are required. However, the cost of raw material 2,4,6-trifluorobenzyl alcohol may be higher, which needs to be weighed.
What to pay attention to when storing and transporting alpha-Bromo-2,4,6-trifluorotoluene
Alpha-bromo-2,4,6-trifluorotoluene is also an organic compound. During storage and transportation, many matters must be paid attention to.
The first priority is safety. This compound may be toxic and irritating, and can cause damage to the human body, such as irritating the eyes, skin and respiratory tract. Therefore, when storing, it should be placed in a cool and well-ventilated place, away from fire and heat sources, and stored separately from oxidants and alkalis. Do not mix storage to prevent dangerous chemical reactions. When transporting, it is also necessary to ensure that the packaging is in good condition to prevent leakage. During transportation, it should be handled with care to avoid collision and friction to prevent material leakage due to package damage.
The second time is related to the environment. If it leaks into the environment, or causes pollution to water, soil, etc. Therefore, the storage area should be equipped with suitable materials to contain leaks, so that they can be collected and treated in time in case of leakage, reducing the harm to the environment. Transportation vehicles should also be equipped with leakage emergency treatment equipment.
Furthermore, its chemical properties are active. Because it contains bromine atoms and trifluoromethyl, it is prone to reactions such as nucleophilic substitution. Avoid contact with substances that can react with it during storage, and prevent interaction with other chemicals during transportation. Storage containers should be made of corrosion-resistant materials, such as glass or specific plastic materials, to ensure that they will not deteriorate due to reaction with the container during storage. The cargo compartment of the transport vehicle should also be kept clean and dry, free of other residues that may cause reactions.
and the storage place should be clearly marked to indicate the danger of the substance, so that the contact person knows to take precautions. Transport personnel must also undergo professional training to be familiar with the characteristics of this compound and emergency treatment methods to ensure that they can properly respond to emergencies during transportation. In this way, alpha-bromo-2,4,6-trifluorotoluene can be properly stored and transported to avoid danger and adverse consequences.