Trifluoro P Toluidine
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
α,α,α-trifluoro-p-toluidine
Chemical Formula C7H6F3N
Molar Mass 161.124 g/mol
Appearance Colorless to light yellow liquid
Boiling Point 197 - 199 °C
Density 1.259 g/cm³
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
Flash Point 77 °C
Odor Characteristic amine - like odor
Cas Number 455 - 14 - 1
Chemical Formula C7H6F3N
Molar Mass 161.124 g/mol
Appearance Colorless to light yellow liquid
Boiling Point 184 - 186 °C
Melting Point N/A
Density 1.248 g/cm³
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
Flash Point 75 °C
Pka N/A
Vapor Pressure N/A
Odor Characteristic amine - like odor
Chemical Formula C7H6F3N
Molecular Weight 161.12
Appearance Colorless to light yellow liquid
Boiling Point 187 - 188 °C
Melting Point N/A
Density 1.258 g/cm³
Flash Point 74 °C
Solubility Soluble in organic solvents
Odor Characteristic amine - like odor
Purity Typically high - purity available in commercial products
Chemical Formula C7H6F3N
Molar Mass 161.124 g/mol
Appearance Colorless to light yellow liquid
Boiling Point 186 - 188 °C
Melting Point N/A
Density 1.274 g/cm³
Flash Point 76 °C
Solubility In Water Insoluble
Vapor Pressure Low
Odor Characteristic amine - like odor
FAQ

What are the main uses of α, α, α-trifluoro-p-toluidine?

α,α,α - trifluoro-p-toluenesulfonic acid, which is used in Dan's formula, is very useful. It is a rare medicine, which can be used as a catalytic agent. In many alchemy methods, it can promote the combination of medicine and increase the effect of medicine.

Cover the alchemy technique, the combination of medicine, often need to help 。α,α,α - trifluoro-p-toluenesulfonic acid has strong catalytic power, which can make various medicines easier to blend and react. In the way of casting swords, if the fire is an alchemy furnace and the medicines are iron stones, this sulfonic acid is like a blast tool, which makes the fire more prosperous, and the iron stone melts quickly and casts a sharp blade. Such as making Dragon and Tiger Great Pill, based on lead and mercury, accompanied by various medicines, adding α,α,α - trifluoro-p-toluenesulfonic acid can make the synthesis of lead and mercury more smooth, and the properties of medicinal pills are more pure.

Furthermore, it can be used for drug adjustment. The medicine of alchemy is rigid and soft, and it is divided into slow 。α,α,α - trifluoro-p-toluenesulfonic acid can be used as a good solution for cattle, according to the nature of the medicine, adjust its rigidity and softness, and slow down its urgency. For example, if you want to make a pill, you need the medicine to be mild and long-lasting, but a certain medicine is stiff. At this time, adding this sulfonic acid can slow down its properties and make the work of the medicinal pill stable and long-lasting.

And when the pill is purified ,α,α,α - trifluoro-p-toluenesulfonic acid also has a wonderful use. It can remove impurities and retain essence, making the pill more superior. You want to take gold from sand, use the ability of sulfonic acid to remove the impurities of sand and gravel, and retain the essence of real gold. Therefore, in the art of alchemy ,α,α,α - although the amount of trifluoro-p-toluenesulfonic acid is not much, it is related to the success or failure of the pill, the pros and cons, and it is an indispensable thing.

What are the physical properties of α, α, α-trifluoro p-toluidine

α,α,α - trifluoroacetophenone, this physical property is also quite specific. Its shape is mostly colorless to light yellow transparent liquid at room temperature, clear and free of impurities, like water in a mirror, calm and bright.

Smell it, the breath is special, although not pungent but unique, like a unique fragrance hidden in the spice jungle, slightly dispersed in the air.

On its boiling point, about a specific value, just like everything has its own track, at a certain temperature node, the molecule breaks free from the shackles of the liquid phase and turns into a gaseous state. The characteristics of this boiling point are crucial in the separation and purification of chemical industry. It can be distilled according to this method to make the mixed things return to their places and achieve a pure state.

As for the melting point, it is also a key physical property. Under a specific low temperature, the thermal movement of molecules gradually slows down, just like a creature sleeping in winter, tends to be arranged in an orderly manner, from a flowing liquid phase to a solid state, such as the condensation of ice, giving it a different form in different environments.

Its solubility is also worth exploring. It may be soluble or insoluble in many organic solvents, just like choosing a suitable residence in the world of solvents. The soluble ones blend with the solvent molecules to form a uniform system; the insoluble ones are distinct and independent. This solubility, in a chemical reaction, can affect the contact of the reactants and the process of the reaction. It is like the driving force behind the chemical reaction stage. Although it is invisible, it controls the rhythm of the reaction.

Density, a parameter that measures its mass per unit volume. Compared with water or other common liquids, it has its specific value. This value is related to its relationship with containers and other substances during storage and transportation, and should not be underestimated.

In addition, its stability is also an important physical property. In a normal environment, if you are in a mild place, do not encounter extreme conditions, and do not encounter specific active substances, you can maintain its inherent structure and properties, just like a calm gentleman, sticking to its own character and not easily moved by the outside world. This stability provides many conveniences for its industrial production, storage and application, enabling it to be effectively used in different scenarios.

What are the chemical properties of α, α, α-trifluoro p-toluidine

α,α,α - trifluoro-p-toluenesulfonyl hydrazone is an important compound in organic synthesis. Its chemical properties are unique and it has many specific reactivity.

Looking at its structure, due to the presence of trifluoromethyl, this group has strong electronegativity, which makes the molecular electron cloud different, thus showing different properties from ordinary sulfonyl hydrazone. In nucleophilic substitution reactions, the presence of trifluoromethyl can greatly affect the activity of the reaction check point. Due to its strong electron-absorbing effect, the carbon atoms connected to it have higher positive electricity and are more vulnerable to attack by nucleophiles. And the two α-groups of the α-position will also affect the reaction, or enhance or weaken the difficulty of attack by nucleophiles, depending on the specific reaction situation.

In the elimination reaction ,α,α,α - trifluoro-p-toluenesulfonyl hydrazone also has a unique performance. Due to the synergistic effect of trifluoromethyl and sulfonyl groups, some chemical bonds in the molecule are more likely to break and rearrange, and then specific elimination products can be achieved. In this process, precise control of reaction conditions is critical, such as temperature, type and dosage of bases, etc., all of which will significantly affect the route and product selectivity of the elimination reaction.

In addition, in the field of metal catalysis ,α,α,α - trifluoro-p-toluenesulfonyl hydrazone can participate as a unique ligand or substrate. Its special electronic structure and steric resistance can form a specific interaction with metal catalysts, induce the reaction to proceed in a unique direction, and realize some transformations that are difficult to achieve by conventional methods.

In summary ,α,α,α - trifluoro-p-toluenesulfonyl hydrazone has shown broad application prospects in the field of organic synthetic chemistry due to its unique chemical properties, and can be used as a powerful tool for constructing complex organic molecular structures.

What is the preparation method of α, α, α-trifluoro p-toluidine

To make α,α,α - trifluoro-p-toluyl, the method is as follows:

Take p-methylbenzoic acid first, place it in a clean kettle, and mix it with an appropriate amount of halogenating agent. This halogenating agent should be selected to introduce fluorine atoms into its structure, such as a specific fluorine-containing halogenating agent, and should be accurately measured according to its reaction ratio. Then, the temperature is controlled in a moderate range. This temperature needs to be confirmed by many tests. If the temperature is too high or side reactions are caused, the reaction will be delayed if it is too low. Stir slowly to make the two fully blend and promote the reaction. < Br >
After the halogenation reaction is completed, the mixture obtained by the reaction is moved to a separator, and the impurities are removed by methods such as distillation and extraction to obtain a product containing α-halogenated p-methylbenzoic acid.

Repeat this product, add it to another reactor, and add an appropriate amount of fluorinating agent. This fluorinating agent also needs to be carefully selected, and its activity and selectivity are related to the success or failure of the reaction. Still controlled temperature and stirred to make the fluorination reaction occur smoothly, so that the halogen atom is gradually replaced by a fluorine atom, and finally α,α,α - trifluoro-p-methylbenzoic acid.

Then, with appropriate reagents, the α,α,α - trifluoride p-toluic acid is acylated. When selecting the acylation reagent, the reaction activity and the effect on the product structure should be considered. Under suitable reaction conditions, such as suitable temperature, presence or absence of catalyst, etc., the acylation is completed, and the final product α,α,α - trifluoride p-toluyl is obtained. The whole process requires fine control of the reaction conditions at each step, paying attention to the purity of the raw material, the dosage, and the reaction time and temperature to obtain a high-purity target product.

What are the precautions for α, α, α-trifluoro-p-toluidine in storage and transportation?

α,α,α - tribromo-p-methoxyacetophenone, many matters should be paid attention to during storage and transportation.

When storing, the temperature and humidity of the environment are the first priority. Although this material is relatively stable, the temperature may be too high, which may cause its properties to change, and even decompose and deteriorate. Therefore, it should be stored in a cool place to ensure its quality. The humidity should not be underestimated. If it is too wet, or the material is damp, it will affect its purity and characteristics.

Furthermore, the storage must be well ventilated. If this substance is stored in a closed space for a long time, the gas emitted may accumulate and cause danger. Good ventilation can avoid this problem and avoid unnecessary reactions with air components.

As for transportation, the packaging must be solid and stable 。α,α,α - tribromo-p-methoxyacetophenone under the bumpy vibration, or there is a risk of damage and leakage. Sturdy packaging can reduce this risk. And during transportation, the temperature should also be controlled, so as not to damage its quality due to drastic changes in external temperature.

In addition, whether stored or transported, it must be kept away from fire and heat sources. This substance may be flammable, and in case of open flames or hot topics, it is easy to cause fires, or even explosions, endangering the safety of people and the environment. It should also be stored and transported separately from oxidants, acids and other substances, because of its active chemical properties, contact with them, or violent reaction, causing disaster.

And when handling, the operator must be careful and wear appropriate protective equipment to prevent contact injury. All these are important items to keep in mind when storing and transporting α,α,α - tribromo-p-methoxyacetophenone.