Chemical Formula | C19H12ClF2 |
Molecular Weight | 314.75 |
Appearance | Solid (usually) |
Melting Point | Data needed |
Boiling Point | Data needed |
Density | Data needed |
Solubility In Water | Low (organic compound, likely sparingly soluble) |
Solubility In Organic Solvents | Good solubility in common organic solvents like benzene, toluene |
Vapor Pressure | Low (due to being a solid, vapor pressure at room temp is low) |
Stability | Stable under normal conditions, but may react with strong oxidizing agents |
Chemical Formula | C19H13ClF2 |
Molecular Weight | 314.76 |
Appearance | Solid (usually) |
Physical State At Room Temperature | Solid |
Solubility In Water | Low (organic compound, likely hydrophobic) |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, toluene |
Odor | Typical organic chemical odor (description may vary) |
Chemical Formula | C20H13ClF2 |
Molecular Weight | 326.77 |
What is the main use of 1- [Chloro (4-fluorophenyl) phenylmethyl] -2-fluorobenzene
1 - [Chloro (4 -fluorophenyl) phenylmethyl] -2 -fluorobenzene is one of the organic compounds. This compound has a wide range of uses and is often a key intermediate in the synthesis of specific drugs in the field of medicinal chemistry.
Looking at the process of drug development and the creation of many new drugs, this compound participates in the construction of core structures. Because of its unique structure, it has a specific activity check point, can interact with targets in organisms, or can regulate physiological and biochemical reactions, so as to achieve the purpose of treating diseases.
In the field of materials science, it also has its uses. Or by virtue of its chemical properties, it can be introduced into polymer materials through specific reactions to improve the properties of materials, such as enhancing the stability and corrosion resistance of materials, or endowing materials with special optical and electrical properties.
Furthermore, in the field of organic synthetic chemistry research, this compound is often used as a starting material or a key reaction intermediate. Organic chemists can modify and modify its structure through various chemical reactions, expand the structural diversity of organic compounds, and lay the foundation for the exploration of new functional materials and bioactive molecules. Therefore, 1 - [chloro (4-fluorophenyl) phenylmethyl] -2 -fluorobenzene is of great significance in many scientific fields, providing an indispensable material basis for related research and applications.
What are the physical properties of 1- [Chloro (4-fluorophenyl) phenylmethyl] -2-fluorobenzene
1 - [Chloro (4 - fluorophenyl) phenylmethyl] - 2 - fluorobenzene, this is an organic compound. Its physical properties are crucial and have a profound impact on its application in various fields.
First of all, the appearance of this compound is usually a colorless to light yellow liquid, or a white to off-white solid, depending on the temperature and environmental conditions. If the temperature is suitable, the molecules are arranged in an orderly order, or in a solid state, with a dense texture; if the temperature rises, the molecular thermal motion intensifies, and it may be transformed into a liquid with good fluidity.
When it comes to the melting point, the melting point of this compound is about [X] ° C. The melting point depends on the strength of the intermolecular forces. There are interactions such as van der Waals forces and hydrogen bonds between the molecules of the compound. When the external temperature reaches the melting point, the molecule obtains enough energy to overcome these forces, and then changes from solid to liquid.
The boiling point is about [X] ° C. The boiling point reflects the temperature conditions required for the transformation of a liquid into a gas. At this temperature, the compound molecules have enough energy to break free from the liquid phase and escape into the gas phase. The boiling point is closely related to factors such as the intermolecular forces and the relative molecular mass. The higher the relative molecular mass, the stronger the intermolecular forces, and the higher the boiling point.
Furthermore, its density is about [X] g/cm ³. Density reflects the mass of a substance per unit volume, and this property is related to the molecular structure and stacking method of the compound. Different molecular structures result in different distances between molecules, which affects the mass per unit volume.
In terms of solubility, this compound is slightly soluble in water. Because most of its molecular structure is hydrophobic aromatic ring structure, it is difficult to form an effective interaction with water molecules, so its solubility in water is very low. However, it is soluble in organic solvents such as dichloromethane, chloroform, and toluene. These organic solvents and the compound molecules can achieve better solubility through the principle of similarity, that is, having similar chemical structures and polarities.
In addition, the compound also has a certain degree of volatility, which will slowly evaporate into the air at room temperature and pressure. Volatility is related to the vapor pressure of the molecule. The higher the vapor pressure, the stronger the volatility. This property requires special attention when storing and using the compound to prevent its escape loss or cause safety problems.
The above are all important physical properties of 1- [Chloro (4-fluorophenyl) phenylmethyl] -2 -fluorobenzene. These properties lay the foundation for further research on its chemical behavior, synthesis methods and practical applications.
What are the chemical properties of 1- [Chloro (4-fluorophenyl) phenylmethyl] -2-fluorobenzene
1-%5BChloro%284-fluorophenyl%29phenylmethyl%5D-2-fluorobenzene is an organic compound with specific chemical properties. Looking at its structure, it is cleverly connected by chlorine-containing, fluorine-containing benzene rings and other parts. In terms of physical properties, it may be a solid state at room temperature, and its structure is relatively stable due to intermolecular forces. And due to the structure of benzene rings, the melting point may be higher. In terms of solubility, considering that it is an organic molecule, according to the principle of similar miscibility, it has good solubility in organic solvents such as dichloromethane and toluene, but poor solubility in water. Because of its weak molecular polarity, it is very different from the polarity of water.
In terms of chemical properties, it has nucleophilic substitution reactivity due to chlorine-containing atoms. Chlorine atoms can be replaced by nucleophilic reagents, such as hydroxyl negative ions, or to And because of its benzene ring structure, it can occur typical reactions of aromatic hydrocarbons, such as electrophilic substitution reaction. The density distribution of the electron cloud of the benzene ring makes it vulnerable to the attack of electrophilic reagents. Under suitable conditions, halogenation, nitrification, sulfonation and other reactions can occur. The presence of fluorine atoms, although enhancing the stability of the molecule, also affects the reactivity and selectivity. Due to the large electronegativity of fluorine atoms, it will absorb electrons, change the electron cloud distribution of the benzene ring, and make the electrophilic substitution reaction check point different.
Furthermore, different groups in the compound interact with each other, such as the interaction between the benzene ring and the chlorobenzyl group and the fluorobenzene ring, or cause its reactivity and chemical properties to be different from those of a single benzene This unique chemical property makes 1-%5BChloro%284-fluorophenyl%29phenylmethyl%5D-2-fluorobenzene have potential application value in the field of organic synthesis, and can be used as intermediates to construct complex organic molecules through various reactions.
What is the synthesis method of 1- [Chloro (4-fluorophenyl) phenylmethyl] -2-fluorobenzene
To prepare 1 - [chloro (4 - fluorophenyl) phenylmethyl] -2 - fluorobenzene, you can follow the following method:
First take an appropriate amount of 2 - fluorobenzaldehyde and place it in a clean reaction vessel. Prepare an organic solvent, such as anhydrous ether, pour it into the reaction vessel in an appropriate amount, so that 2 - fluorobenzaldehyde is fully dissolved to form a uniform solution.
In a separate container, react magnesium strips with halogenated hydrocarbons (such as 4 - fluorobromobenzene) to prepare Grignard's reagent. When Grignard's reagent is made, slowly drop it into a solution containing 2 - fluorobenzaldehyde under low temperature and stirring conditions. This process requires strict temperature control, and the temperature should not be too high to prevent side reactions from occurring. Add it dropwise and continue to stir for a period of time to make the reaction fully proceed.
Then, the reaction mixture is carefully treated with a dilute acid solution to promote the hydrolysis of the intermediate product. After the hydrolysis is completed, the organic phase is extracted with a suitable organic solvent and collected. Then the water in the organic phase is removed with a desiccant such as anhydrous sodium sulfate.
After the water is removed, the organic phase is distilled, first distilled under atmospheric pressure to remove the organic solvent, and then distilled under reduced pressure to collect fractions in a specific boiling point range. The crude product
needs further purification and can be obtained by column chromatography. Select the appropriate silica gel as the stationary phase, and use a specific proportion of petroleum ether and ethyl acetate mixture as the mobile phase for column chromatographic separation. Carefully collect the eluent containing the target product and steam off the solvent to obtain pure 1- [chloro (4-fluorophenyl) phenylmethyl] -2 -fluorobenzene. The whole process requires fine operation at each step, and the conditions must be precisely controlled to obtain satisfactory results.
What is the price range of 1- [Chloro (4-fluorophenyl) phenylmethyl] -2-fluorobenzene in the market?
I have not heard of the exact price range of "1 - [Chloro (4 - fluorophenyl) phenylmethyl] - 2 - fluorobenzene" in the market. The price of this compound may fluctuate due to various factors such as use, purity, market supply and demand. If it is used for scientific research, the purity requirements are quite high, and the price is high; if it is used for large-scale industrial production, the price depends on the output and cost.
And its price is also affected by regions. The market in different countries and regions varies due to logistics, taxes, and competition, and the price is difficult to determine. In addition, the chemical market is unpredictable, and raw material prices, policies and regulations, etc., can make its prices fluctuate. Therefore, if you want to know the market price range, you must carefully check the chemical product trading platform, supplier quotations, or consult industry insiders to obtain more accurate price information.