Chemical Formula | C7H7F |
Molar Mass | 110.13 g/mol |
Appearance | Colorless liquid |
Odor | Aromatic odor |
Density | 1.00 g/cm³ at 25 °C |
Boiling Point | 114 - 116 °C |
Melting Point | -87 °C |
Flash Point | 17 °C |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in many organic solvents |
Vapor Pressure | 5.33 kPa at 25 °C |
Refractive Index | 1.472 - 1.474 at 20 °C |
Chemical Formula | C7H7F |
Molar Mass | 110.13 g/mol |
Appearance | Colorless liquid |
Boiling Point | 114 - 115 °C |
Melting Point | -87.3 °C |
Density | 1.005 g/cm³ at 20 °C |
Vapor Pressure | 12.7 mmHg at 25 °C |
Flash Point | 15 °C |
Solubility In Water | Insoluble |
Odor | Aromatic odor |
Chemical Formula | C7H7F |
Molar Mass | 110.13 g/mol |
Appearance | Colorless liquid |
Boiling Point | 115 - 116 °C |
Melting Point | -87.7 °C |
Density | 1.009 g/cm³ at 20 °C |
Solubility In Water | Insoluble |
Vapor Pressure | 13.3 hPa at 20.5 °C |
Flash Point | 12 °C |
Refractive Index | 1.472 - 1.474 |
Chemical Formula | C7H7F |
Molecular Weight | 110.13 |
Appearance | Colorless liquid |
Boiling Point | 115 - 117 °C |
Melting Point | -87.7 °C |
Density | 1.002 g/cm³ at 20 °C |
Flash Point | 12 °C |
Solubility In Water | Insoluble |
Vapor Pressure | 5.33 kPa at 24.6 °C |
Refractive Index | 1.472 (20 °C) |
What are the main uses of 3-fluorotoluene?
3-Fluorotoluene, also known as m-fluorotoluene, is an organic compound and is widely used in the chemical industry. Its main uses are as follows:
First, it is used as an intermediate in pharmaceutical synthesis. In pharmaceutical chemistry, it is a key raw material and can be converted into a variety of pharmaceutical components through a series of chemical reactions. For example, when synthesizing specific antibacterial drugs, 3-fluorotoluene is replaced and oxidized to build key structural fragments. These drugs have significant efficacy in treating specific diseases.
Second, it is used in pesticide synthesis. In agricultural production, pesticides are important materials to ensure crop yield and quality. 3-Fluorotoluene can be used as a starting material for the synthesis of new pesticides. With its special chemical structure, it gives pesticides unique biological activities, such as high-efficiency poisoning effect on specific pests, or good control effect on certain plant diseases, and helps agricultural harvest.
Third, as an important raw material for material synthesis. In the field of materials science, 3-fluorotoluene can participate in the synthesis of high-performance polymer materials. After polymerization, its structural units are integrated into the polymer chain, giving the material special properties, such as enhancing the heat resistance and chemical stability of the material. It is widely used in high-end fields such as aerospace and electronics to meet the strict performance requirements of materials.
Fourth, used in dye synthesis. In the dye industry, 3-fluorotoluene is used as a basic raw material to introduce different functional groups through multi-step reactions to synthesize dye molecules with diverse structures. These dyes have bright color and good stability, and are widely used in textile, printing and dyeing industries to meet the market demand for various color and performance dyes.
What are the physical properties of 3-fluorotoluene?
3-Fluorotoluene is a genus of organic compounds. It has the following physical properties:
In terms of concept, it is a colorless and transparent liquid that exists stably at room temperature and pressure. Smell, there is a specific aromatic smell, but this smell should not be smelled for a long time, because it is toxic and irritating, or harmful to human health.
When talking about the boiling point, it is about 116-117 ° C. At this temperature, 3-fluorotoluene gradually changes from liquid to gaseous state. This boiling point characteristic is very important in chemical operations such as separation and purification. If the method of distillation is carried out, 3-fluorotoluene can be separated from the mixture according to its boiling point. < Br > Its melting point is about -87.3 ° C. When the temperature drops below the melting point, 3-fluorotoluene will solidify from liquid to solid. Knowing the melting point, it is essential to consider the effect of ambient temperature on the state of substances during storage and transportation.
The density of 3-fluorotoluene is about 1.025g/cm ³, which is slightly heavier than water. In systems involving liquid-liquid mixing, this density difference can cause the stratification of liquids with different densities such as 3-fluorotoluene and water, which facilitates separation operations.
In terms of solubility, 3-fluorotoluene is insoluble in water, but can be miscible with organic solvents such as alcohols, ethers, and benzene. This solubility characteristic is crucial in the selection of suitable solvents in organic synthesis and chemical reactions. Many organic reactions need to be carried out smoothly in a specific solvent environment. 3-fluorotoluene can be used as a solvent or combined with other organic solvents to provide a suitable medium for the reaction.
What are the chemical properties of 3-fluorotoluene?
3-Fluorotoluene has unique chemical properties and is worth exploring. This substance is an organic compound with dual characteristics of aromatic hydrocarbons and halogenated hydrocarbons.
First talk about its physical properties. At room temperature, it is mostly a colorless and transparent liquid with an aromatic odor. It is miscible with many organic solvents, such as ethanol and ether. Its boiling point is about 116-118 ° C, and its density is less than that of water, so it will float in the upper layer in water.
From the perspective of chemical activity, the electron cloud density of the benzene ring of 3-fluorotoluene changes due to the presence of fluorine atoms. Although fluorine atoms have electron-withdrawing induction effects, their lone pair electrons can be conjugated with the benzene ring to stabilize the benzene ring to a certain extent. This property makes the electrophilic substitution activity of benzene ring different from that of toluene.
In the electrophilic substitution reaction, the fluorine atom is an ortho-and para-site locator. If nitrification occurs, the nitro group is mainly introduced into the adjacent and para-site of the fluorine atom to form products such as 2-nitro-3-fluorotoluene and 4-nitro-3-fluorotoluene. Due to the electron-absorbing induction effect of the fluorine atom, the reaction activity is slightly lower than that of toluene, and slightly more intense reaction conditions are required.
Its side chain methyl can be oxidized. Treated with a strong oxidant such as acidic potassium permanganate, the methyl can be oxidized to a carboxyl group to obtain 3-fluorobenzoic acid. And the hydrogen atom of methyl group has a certain activity. Under the action of light or initiator, halogenation reaction can occur, and halogens such as chlorine and bromine can replace the hydrogen of methyl group.
In the field of metal organic chemistry, 3-fluorotoluene can participate in the coupling reaction catalyzed by palladium. With reagents such as borate esters or halogenated aromatics, in the presence of suitable ligands and bases, carbon-carbon bond coupling can be realized to synthesize complex organic molecules, which are widely used in drug synthesis, materials science and other fields.
3-fluorotoluene is rich in chemical properties and exhibits diverse reactivity based on its structural characteristics. It plays an important role in many aspects of organic synthesis and provides key raw materials and intermediates for the creation of new compounds, the development of new materials and drugs.
What are the production methods of 3-fluorotoluene?
3-Fluorotoluene, as well as organic compounds, can be prepared by several methods.
One is to use toluene as the starting material and prepare it by halogenation reaction. Under appropriate reaction conditions, toluene interacts with fluorine-containing halogenated reagents. If cobalt trifluoride (CoF
) is used as a fluorinating agent, at a specific temperature, pressure and catalyst, the methyl ortho-hydrogen atom of toluene can be replaced by a fluorine atom to obtain 3-fluorotoluene. This reaction process is more complicated, requiring precise temperature control and pressure control, and the choice and dosage of catalyst have a great influence on the reaction.
The second can be started from m-methylaniline. First, m-methylaniline is diazotized to form a diazonium salt, and then interacts with fluoroboronic acid to form m-methylbenzene diazonium fluoroborate. Then it is decomposed by heating to obtain 3-fluorotoluene. This process of diazotization needs to be carried out in a low temperature environment to prevent the decomposition of diazonium salts, and then the thermal decomposition step also needs to pay attention to the control of temperature to ensure the smooth progress of the reaction and improve the yield of the product.
Third, 3-fluorotoluene can be prepared by halogen exchange fluorination reaction with m-chlorotoluene as raw material. In this reaction, a suitable fluorination reagent, such as potassium fluoride (KF), needs to be selected, and a phase transfer catalyst is added to promote the reaction. The solvent selection of the reaction system is also critical to ensure that the fluorinated reagent has good solubility with m-chlorotoluene and does not interfere with the reaction.
Each method for preparing 3-fluorotoluene has its own advantages and disadvantages. Halogenation reaction raw materials are easy to obtain, but the reaction conditions are harsh; preparation from m-methylaniline, the steps are slightly more complicated, but higher purity products can be obtained; halogen exchange fluorination reaction is relatively mild, and the cost and recovery of phase transfer catalysts may be factors to consider. When actually preparing, the most suitable method should be selected according to many factors such as actual demand, raw material availability and cost.
What should be paid attention to when storing and transporting 3-fluorotoluene?
3-Fluorotoluene is also an organic compound. When storing and transporting, it is necessary to exercise caution to ensure safety.
First word storage. This substance should be placed in a cool and ventilated warehouse. Because of the cool environment, its volatilization rate can be reduced, and good ventilation can prevent its accumulation in a limited space from causing excessive concentration and causing danger. The temperature of the warehouse should be controlled within an appropriate range, and it should not be too high, so as not to promote chemical reactions or exacerbate volatilization. And keep away from fire and heat sources, both of which can cause it to burn or even explode, because 3-fluorotoluene is flammable. At the same time, it should be stored separately from oxidants, acids, bases, etc., and should not be mixed. The edge oxidizer meets with 3-fluorotoluene, or triggers a violent oxidation reaction; the interaction of acid and alkali with it may also cause the chemical reaction to go out of control, endangering safety. The storage area should also be equipped with suitable materials to contain the leakage, in case of leakage, it can be dealt with in time to prevent its spread from causing greater harm.
Secondary transportation. Before transportation, be sure to ensure that the packaging is complete and sealed. A good packaging can prevent its leakage, and a seal can prevent air, moisture, etc. from contacting it and avoid unnecessary reactions. During transportation, make sure that the container does not leak, collapse, fall, or damage. When handling, it should be handled lightly. Do not operate brutally. 3-fluorotoluene leaks due to impact, vibration, etc., or damage to the packaging. Transportation vehicles must be equipped with the corresponding variety and quantity of fire fighting equipment and leakage emergency treatment equipment. If there is an accident such as a leak on the way, rescue and treatment can be carried out immediately. And when transporting, drive according to the specified route and do not stop in densely populated areas and residential areas to prevent leakage from causing harm to the public.