3 Fluoro Trifluoro Toluene
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
3-fluoro-α,α,α-trifluoro toluene
Chemical Formula C7H4F4
Molecular Weight 164.10
Appearance Colorless liquid
Odor Characteristic odor
Boiling Point 102 - 103 °C
Melting Point -58 °C
Density 1.307 g/mL at 25 °C
Solubility In Water Insoluble
Vapor Pressure 12.5 mmHg at 25 °C
Flash Point 10 °C
Refractive Index 1.386 at 20 °C
FAQ

3 - fluoro -α,α,α- what is the main use of tri fluoro toluene

3-Fluorine -α,α,α - trifluorotoluene, this substance is widely used. In the field of organic synthesis, it is a crucial intermediate. Many fluorine-containing organic compounds can be prepared through a series of chemical reactions. Fluorine-containing compounds have shown unique properties in medicine, pesticides, materials, etc.

In the field of medicine, with its special structure and properties, it can participate in the synthesis of drugs with high efficiency, low toxicity and high selectivity. Due to the introduction of fluorine atoms, it can change the electron cloud density and fat solubility of drug molecules, thereby improving the biological activity and metabolic stability of drugs. For example, some drugs for the treatment of cardiovascular diseases and nervous system diseases use 3-fluoro -α,α,α - trifluorotoluene as a key intermediate in the synthesis process. After multi-step reaction, a specific drug molecular structure is constructed, which brings good news to patients.

In terms of pesticides, it can be used to prepare high-efficiency, low-residue and environmentally friendly fluorinated pesticides. The presence of fluorine atoms enhances the effect of pesticides on pest targets, improves the shelf life of pesticides, reduces the frequency and dosage of application, and reduces the negative impact on the environment. Like the development of some new pesticides and fungicides, 3-fluoro -α,α,α - trifluorotoluene plays an indispensable role in the sustainable development of agriculture.

In the field of materials science, it can participate in the synthesis of high-performance fluorinated materials. Fluoropolymer materials are widely used in aerospace, electronics, construction and other industries due to their excellent weather resistance, chemical corrosion resistance, and low surface energy. For example, in the aerospace field, fluoropolymer coatings can be used to protect the surface of aircraft and resist harsh environmental erosion; in electronic appliances, fluorinated materials can be used to make high-performance insulating materials and sealing materials to ensure the stable operation of electronic equipment. This highlights the important value of 3 - -α,α,α - trifluorotoluene in material synthesis.

3 - fluoro -α,α,α- what are the physical properties of tri fluoro toluene

3 - fluoro - α,α,α - tri fluoro toluene, the Chinese name is often 3-fluorotrifluorotoluene. This is a chemical compound, with multi-physical properties, and is widely used in many fields.

Its outer color is usually transparent, and the taste is special. The smell of the solution is slightly irritating. Under normal conditions, the boiling temperature is 102-103 ℃. This characteristic makes it easy to reduce the temperature at a specific temperature during operations such as adding or steaming. Melting temperature - 70 ℃, low melting temperature shows that it can still hold liquid in low temperature environments, exhibiting good fluidity.

has a density of nearly 1.32 g/cm ³, which is heavier than water. If mixed with water, it will sink to the bottom of the water. It is insoluble in water, because the molecules are mainly non-carbon-carbon and carbon-fluorine, and the action force of non-water molecules is weak. But it is soluble in many soluble substances, such as ether, acetone, benzene, etc. Due to the principle of similar phase dissolution, it is non-soluble or weakly soluble.

This compound is not soluble, and it is easy to form under normal conditions, resulting in a certain amount of evaporation in the air. Its evaporation is heavier than the air, and it can be dispersed at a low phase distance. It may be reignited in case of fire.

Its chemical activity is active, and the presence of fluorine atoms increases its anti-activity. The fluorine atom on benzene can be nucleated and substituted. Trifluoromethyl at the α position reduces the density of benzene sub-clouds, and benzene is more likely to be substituted and substituted. Due to its characteristics, 3-fluorotrifluorotoluene is used in the synthesis of benzene. It is also used as a raw material in the field, and the synthesis is efficient and low toxic. In the field of materials, it can be used to synthesize fluorine-containing polymer materials to improve the corrosion resistance and weather resistance of materials.

3 - fluoro -α,α,α- what are the chemical properties of tri fluoro toluene

3-Fluorine -α,α,α - trifluorotoluene is an important compound in organic chemistry. It has unique chemical properties and has a great impact on the field of organic synthesis and materials science.

This compound is the first to have significant chemical stability. Due to the large number of fluorine atoms in the molecule and the high carbon-fluorine bond energy, the substance is not easy to react with other substances under normal conditions. In many chemical reaction environments, it can maintain its own structure intact, like a strong fortress, which is difficult to be easily broken by external chemical action.

Secondly, it has high fat solubility. Due to the large electronegativity of fluorine atoms, the molecular polarity changes, making the compound more soluble in organic solvents. This property is of great significance in drug development. If the drug molecule has good fat solubility, it can more easily penetrate the biofilm and improve the bioavailability of the drug. It is like a delicate key that can smoothly open the absorption channel in the organism.

Furthermore, the reactivity of 3-fluoro -α,α,α - trifluorotoluene is unique. Although the overall stability is good, under specific conditions and the assistance of catalysts, substitution reactions can occur at specific locations in the molecule. For example, the fluorine atom on the benzene ring can be replaced by other functional groups, thereby introducing new chemical structures, providing the possibility of synthesizing more complex organic compounds, like building blocks, on which a variety of molecular structures can be constructed.

In addition, the volatility and boiling point of this compound are also characterized. Due to the influence of fluorine atoms, its boiling point and volatility are different from those of compounds with similar structures. Appropriate volatility is crucial in the application of industrial products such as coatings and cleaning agents. It can ensure that the product evaporates in a timely manner during use and exert the expected effect. Like a precise dancer, it shows its own value in the industrial stage according to the established rhythm.

3 - fluoro -α,α,α- tri fluoro toluene

3-Fluoride -α,α,α - trifluorotoluene, there are many synthesis methods. There are several common methods mentioned above.

First, 3-fluorotoluene is used as the starting material and is obtained by selective fluorination. First, with appropriate fluorination reagents, such as Selectfluor, etc., under suitable reaction conditions, such as in an organic solvent, temperature control and catalyst are added to gradually replace the hydrogen atom on the methyl group with a fluorine atom, and the final product is obtained. This process requires fine regulation of the reaction conditions. Due to the high activity of fluorination, it is easy to cause excessive fluorination or other side reactions. < Br >
Second, starting from 3-chloro -α,α,α - trifluorotoluene, it is prepared by halogen exchange reaction. Fluoride salts, such as potassium fluoride, are heated in an appropriate solvent in the presence of a phase transfer catalyst. The phase transfer catalyst can promote the transfer of ions between the organic phase and the aqueous phase, and improve the reaction efficiency. It is necessary to pay attention to the selection of suitable solvents and reaction temperatures to avoid other side reactions of chlorine atoms and ensure that fluorine atoms selectively replace chlorine atoms.

Third, fluorophenyl ring derivatives are synthesized by coupling reaction with fluorohalogenated hydrocarbons. For example, 3-fluoroborate phenyl ester and trifluoromethyl halogenated hydrocarbons are coupled under the action of transition metal catalysts such as palladium catalysts in basic conditions and appropriate solvents. This reaction requires high purity of the reaction substrate, activity and dosage of the catalyst, and the reaction conditions need to be strictly controlled to obtain higher yields of 3-fluoro -α,α,α - trifluorotoluene.

3 - fluoro -α,α,α- tri fluoro toluene in the use of what are the precautions

3-Fluoride -α,α,α - trifluorotoluene. When using this product, many things must be paid attention to.

Bear the brunt and safety is the key. This is a volatile organic compound with a pungent smell and may irritate the eyes, respiratory tract and skin. When operating, be sure to do it in a well-ventilated place, preferably in a fume hood to avoid inhalation of volatile gas, and wear appropriate protective equipment, such as protective glasses, masks and gloves, to prevent direct contact with the skin and eyes. In case of accidental contact, rinse with plenty of water immediately. If you feel unwell, seek medical treatment as soon as possible.

Furthermore, the chemical properties cannot be ignored. As an organic reagent, when it participates in chemical reactions, its activity and reaction characteristics are different due to the presence of fluorine atoms. Before use, it is necessary to have a thorough understanding of the relevant chemical reaction mechanism and conditions, and to precisely control the reaction temperature, time, and proportion of reactants. Otherwise, the reaction results may deviate from expectations, or even cause side reactions. For example, in some nucleophilic substitution reactions, the presence of fluorine atoms may affect the reaction rate and product selectivity.

Storage is also important. It should be stored in a cool, dry and well-ventilated place, away from fire sources and oxidants. Because of its flammability, it is dangerous to encounter open flames, hot topics or combustion. Contact with oxidants, or cause violent reactions, endangering safety.

In addition, in view of environmental considerations, the waste generated during use must not be discarded at will. It needs to be collected in accordance with relevant regulations, handed over to professional treatment institutions, and properly handled to prevent pollution to the environment. In short, the use of 3-fluoro -α,α,α - trifluorotoluene should be treated with caution in many aspects such as safety, chemical properties, storage and environmental protection.