Chemical Formula | C7H6ClF |
Molar Mass | 144.57 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | 172 - 174 °C |
Density | 1.23 g/cm³ |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents |
Flash Point | 63 °C |
Odor | Pungent |
Chemical Formula | C7H6ClF |
Molar Mass | 144.57 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | 173 - 175 °C |
Density | 1.246 g/mL at 25 °C |
Flash Point | 61 °C |
Solubility | Insoluble in water, soluble in organic solvents like ethanol, ether |
Refractive Index | 1.5065 - 1.5085 (20 °C) |
What are the main uses of Ortho-Fluorobenzyl Chloride?
O-fluorobenzyl chloride has a wide range of uses. In the field of organic synthesis, it is often a key raw material. It can be used to prepare various fluorine-containing organic compounds, which is due to the characteristics of fluorine atoms and benzyl chloride in its structure.
covers organic synthesis, seeking products with novel structures and unique properties. The fluorine atom in o-fluorobenzyl chloride has strong electronegativity, which can change the electron cloud distribution of molecules and make the products exhibit unique physical and chemical properties. Therefore, it is very important to prepare fluorine-containing drugs, pesticides, etc.
In pharmacies, with o-fluorobenzyl chloride as the starting material, through a series of chemical reactions, molecular structures with specific pharmacological activities can be constructed. The introduction of fluorine atoms may enhance the interaction between drugs and targets, improve the efficacy of drugs, or improve their metabolic stability and prolong the time of action in the body.
In the field of pesticides, fluorinated pesticides have become a hotspot in research and application due to their high efficiency, low toxicity and environmental friendliness. Pesticides made from o-fluorobenzyl chloride have high selectivity and strong lethality to pests, and have a short residual period in the environment, which is conducive to the protection of the ecological environment.
Furthermore, in the field of materials science, it also has its application. After chemical reaction, the introduction of its structure into polymer materials can endow the materials with special properties, such as improving the corrosion resistance and thermal stability of the materials, so that the materials have better application performance in special environments.
What are the physical properties of Ortho-Fluorobenzyl Chloride?
O-fluorobenzyl chloride is one of the organic compounds. It has specific physical properties and is very important in the field of organic synthesis.
In terms of its properties, o-fluorobenzyl chloride is mostly colorless to slightly yellow liquid at room temperature, and it is clear and transparent. It is volatile to a certain extent and may smell a special odor in the air.
Its boiling point is specific, about a certain temperature range. This temperature can change o-fluorobenzyl chloride from liquid to gaseous. The melting point is also a fixed value. Below this temperature, the substance is solid.
The density of o-fluorobenzyl chloride is different from that of water. It is placed in water, floating or sinking, depending on the comparison of its density with water. Its solubility is also a key property, soluble in some organic solvents, such as ethanol, ether, etc., but poor solubility in water.
Furthermore, its refractive index is also a parameter characterizing physical properties. When light passes through o-fluorobenzyl chloride, its refractive index is specific, and this value can help identify and analyze the substance.
The vapor pressure of o-fluorobenzyl chloride also has a corresponding value, which is related to its equilibrium between the gas phase and the liquid phase at a certain temperature.
In summary, the physical properties of o-fluorobenzyl chloride, such as color, state, taste, boiling point, melting point, density, solubility, refractive index, vapor pressure, etc., are all important for the understanding and application of this compound. In many fields such as organic synthesis, with these properties, many operations such as separation, purification, and setting of reaction conditions can be reasonably planned.
What are the chemical properties of Ortho-Fluorobenzyl Chloride?
Ortho-Fluorobenzyl Chloride is an important chemical raw material in organic synthesis. It has the general nature of halogenated hydrocarbons, active chemical properties and diverse reactions.
First, nucleophilic substitution reaction. Due to the strong electronegativity of chlorine atoms in the molecule, the C-Cl bond polarity is very strong, and chlorine atoms are easily replaced by nucleophiles. In case of alcohol nucleophiles, under alkali catalysis, chlorine atoms can be substituted with alkoxy groups to form corresponding ether compounds; when reacted with ammonia or amines, nitrogen-containing derivatives can be formed, which is common in the preparation of drugs, pesticides and fine chemicals.
Second, hydrolysis reaction. Under alkaline conditions, o-fluorobenzyl chloride can be hydrolyzed. The hydroxyl group in the water molecule attacks the carbon atoms connected to chlorine as a nucleophilic reagent, and the chlorine atoms leave, and finally form o-fluorobenzyl alcohol through a series of reactions. This reaction requires controlled conditions, due to excessive reaction or side reactions.
Third, react with metal-organic reagents. For example, with Grignard reagents, nucleophilic addition reactions can occur to form new carbon-carbon bonds. This is an important means to grow carbon chains and build complex molecular structures in organic synthesis, laying the foundation for the synthesis of organic compounds with special structures.
Fourth, elimination reaction. Under the action of strong bases, o-fluorobenzyl chloride can undergo an elimination reaction to remove hydrogen chloride and form unsaturated compounds containing carbon-carbon double bonds. This reaction is of great significance for the preparation of organic intermediates with specific unsaturated structures.
However, it should be noted that o-fluorobenzyl chloride has certain toxicity and irritation, and strict protective measures should be taken during operation to ensure experimental safety and personnel health. And in the application of organic synthesis, the reaction conditions should be carefully adjusted according to the structure of the target product and the reaction requirements to achieve the best reaction effect.
What is the production method of Ortho-Fluorobenzyl Chloride?
The method of preparing o-fluorobenzyl chloride has been studied by many chemists in the past. One method is to take o-fluorotoluene as the starting material and obtain it through chlorination reaction. First put o-fluorotoluene in a suitable reactor, add an appropriate amount of initiator, such as azobisisobutyronitrile, this initiator can promote the initiation of the reaction. Then, chlorine gas is introduced, and the reaction temperature should be controlled within a certain range, usually about 80-120 degrees Celsius. Chlorine gas is slowly introduced. At this temperature, the hydrogen atom in the benzyl position of o-fluorotoluene is gradually converted into o-fluorobenzyl chloride by the substitution of chlorine atoms. In this reaction process, the reaction process needs to be closely monitored, and analytical methods such as gas chromatography can be used to detect the degree of reaction and the purity of the product.
There are other methods, using o-fluorobenzoic acid as the starting material. First, the o-fluorobenzoic acid is converted into o-fluorobenzyl alcohol through reduction reaction. Commonly used reducing agents, such as sodium borohydride-zinc chloride system, can be effectively reduced in a suitable solvent, such as tetrahydrofuran, to produce o-fluorobenzyl alcohol. Then, the o-fluorobenzyl alcohol interacts with chlorination reagents, such as reacting with sulfoxide chloride under heating conditions, and the hydroxyl group of the o-fluorobenzyl alcohol can be replaced by chlorine atoms to obtain o-fluorobenzyl chloride. Although this method is a little complicated, it can obtain a higher purity product. < Br >
Preparation of o-fluorobenzyl chloride, each has its own advantages and disadvantages, and the party should choose it carefully according to actual needs, such as the availability of raw materials, cost, product purity and other factors, in order to improve the situation.
What is the market price of Ortho-Fluorobenzyl Chloride?
Orthogonal-fluorobenzyl chloride, in a word, is influenced by factors such as the availability of the market. In the past, the price of this chemical substance was determined by factors such as the supply and demand, the ease of manufacture, and the cost of raw materials.
If there is a supply and demand, the demand for orthogonal-fluorobenzyl chloride in the market is strong, and the supply phase is scarce, and it will be lost; on the contrary, if the demand is low, the supply will be full, and the supply will decline.
The ease of manufacture is also low. The cost of orthogonal-fluorobenzyl chloride may require delicate engineering and complex processes. If so, the cost of production will be high, and the market will also rise. If the method is easy and the cost is controlled, the price is expected to be lower or slightly lower.
The cost of raw materials should not be ignored either. The cost of raw materials required for the production of orthogonal-fluorobenzyl chloride will directly reduce the market value of the finished product. If the raw material is high, the finished product will also be low; if the raw material is low, the finished product may have room for a decrease.
In addition, the market is still affected by factors such as regional differences, seasonal fluctuations, and policy laws. Therefore, in order to know the market value of orthogonal-fluorobenzyl chloride, the latest market conditions in the chemical industry, the information of various suppliers, and the above-mentioned factors can be obtained.