Chemical Formula | C8H6F2O2 |
Molar Mass | 172.13 g/mol |
Appearance | White to off - white solid |
Melting Point | 110 - 114 °C |
Solubility In Water | Slightly soluble |
Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, acetone |
Pka | Around 3 - 4 (weakly acidic) |
Chemical Formula | C8H6F2O2 |
Molar Mass | 172.13 g/mol |
Appearance | Solid (usually white or off - white) |
Solubility In Water | Low solubility |
Solubility In Organic Solvents | Soluble in some organic solvents like ethanol, acetone |
Melting Point | Typically around 100 - 110 °C |
Pka Value | Indicates acidic nature, around 3 - 4 |
Density | Data varies, but around 1.3 - 1.4 g/cm³ |
Chemical Formula | C8H6F2O2 |
Molar Mass | 172.13 g/mol |
Appearance | White to off - white solid |
Melting Point | 113 - 117 °C |
Solubility In Water | Slightly soluble |
Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, dichloromethane |
Pka | Around 3.9 (approximate value for the carboxylic acid group) |
Odor | Odorless or very faint odor |
What are the main uses of 2,6-difluorophenylacetic acid?
2% 2C6-diethylnaphthalene acetic acid is also a plant growth regulator. Its main uses are roughly three.
First, it can promote plant rooting. When cuttings propagate, treating the base of cuttings with an appropriate amount of 2% 2C6-diethylnaphthalene acetic acid can significantly increase the generation of adventitious roots. Because this substance can stimulate the division and differentiation of plant cells, make the base cells of cuttings active abnormally, accelerate the formation of callus, and then give birth to many robust adventitious roots, which can improve the survival rate of cuttings. Cuttings of plants such as mulberry, tea, osmanthus, etc. are quite effective.
Second, it can prevent flowers and fruits from falling. In the flowering and young fruit stages of plants, moderate application of 2% 2C6-diethylnaphthalene acetic acid can regulate the hormone balance in plants, enhance the connection between the fruit stalk and the branches, so that the young fruit can be firmly attached, and avoid falling flowers and fruits due to physiological disorders. Crops such as apples, citrus, tomatoes, etc., can often keep flowers and fruits after application, improve fruit setting rate and increase yield.
Third, can improve fruit development. During the fruit expansion period, rational application of 2% 2C6-diethylnaphthalene acetic acid can promote the expansion and division of fruit cells, increase fruit volume, and improve fruit quality, such as making the fruit more colorful and sugar content increased. In the cultivation of grapes, strawberries and other fruits, timely and appropriate use can obtain high-quality fruits.
2% 2C6-diethylnaphthalene acetic acid plays a key regulatory role in many stages of plant growth, and is a commonly used and important substance in agricultural production and horticultural cultivation.
What are the physical properties of 2,6-difluorophenylacetic acid?
2% 2C6-diethylaminocaproic acid, white to pale yellow crystalline powder, odorless and slightly bitter in taste. Its melting point is between 46 and 48 ° C, and it is relatively stable at room temperature and pressure. It is easily soluble in organic solvents such as chloroform, ether, and acetone, and has a certain solubility in water, but the solubility is not high.
Its properties determine that it needs to be stored in a dry, cool and well-ventilated place to avoid contact with strong oxidants, strong acids, strong bases, etc., to prevent chemical reactions from occurring and causing deterioration. Due to its fat solubility, it is often used as an organic intermediate in the field of organic synthesis, participating in the synthesis of many important compounds, and has certain application value in many disciplines such as medicinal chemistry and materials science. Due to its unique chemical structure and physical properties, it can play a key role in the generation of substances with special properties and uses under specific reaction conditions.
Is the chemical properties of 2,6-difluorophenylacetic acid stable?
2% 2C6-diethylphenylacetic acid is an organic compound. The stability of its chemical properties depends on the environment and reaction conditions.
This compound contains functional groups such as benzene ring and carboxyl group. The benzene ring has a certain stability because its conjugate system can disperse the electron cloud and stabilize the structure. However, the ethane group on the benzene ring may affect the electron cloud distribution of the benzene ring, making it more likely to participate in the electrophilic substitution reaction, which is slightly less stable than benzene. The presence of the carboxyl group makes the compound acidic. In aqueous solution, the carboxyl group can be partially ionized to release hydrogen ions. The strength of its acidity is related to the surrounding substituents. In this compound, the ethane group is the power supply group, or the carboxyl group is slightly less acidic than acetic acid.
In terms of oxidation reaction, the ethyl group of the compound can be oxidized to form corresponding carboxylic acids or other oxidation products. In case of strong oxidants, the benzene ring may also be oxidized and destroyed. However, under mild conditions, if there is no specific catalyst and suitable reaction conditions, the benzene ring is relatively stable and not easy to be oxidized.
Under normal storage conditions, if placed in a cool, dry and dark environment, away from strong oxidants, strong acids and strong bases, 2% 2C6-diethylphenylacetic acid may maintain a certain stability, and the chemical properties change slowly. However, once it is under specific reaction conditions, such as high temperature and catalyst existence, various chemical reactions may occur, and the stability will be destroyed.
In summary, the chemical stability of 2% 2C6-diethylphenylacetic acid is not absolute and will vary depending on the environment and reaction conditions.
What are the preparation methods of 2,6-difluorophenylacetic acid?
For 2% 2C6-diethylnaphthalene acetic acid, there are various methods for preparation. One method is to use naphthalene as the base, through the reaction of acylation, the acetyl is introduced on the naphthalene ring, and the reaction conditions, such as temperature and the ratio of reagents, should be well controlled to make the acetylation position accurate. The reagent used for acylation, when it is acetyl halide or acid anhydride, is assisted by an appropriate catalyst to make the reaction smooth.
Then, the resulting acetyl naphthalene derivative is treated with a halogenating agent, so that a halogen atom is introduced at a specific position. The choice of halogenating agent is related to the efficiency of the reaction and the purity of the product, so it should be done with caution. The reaction of halogenation can often be carried out with halogenated elements or halogenated reagents in suitable solvents.
Then the halogenated acetyl naphthalene interacts with ethylene dihalide. In an alkaline environment, a nucleophilic substitution reaction occurs, and the two are connected to form a 2% 2C6-diethylnaphthalene-acetic acid precursor. In this step, the strength of the base and the properties of the solvent are all key factors and need to be carefully regulated.
Finally, the precursor is hydrolyzed and acidified to generate 2% 2C6-diethylnaphthalene-acetic acid. When hydrolyzing, choose the appropriate base or acid to control the process and degree of the reaction. When acidifying, adjust to the appropriate pH value to precipitate the product, and obtain pure 2% 2C6-diethylnaphthalene acetic acid.
There are other methods, or start with naphthol, etherification, alkylation and other series of reactions to gradually build the structure of the molecule, and 2% 2C6-diethylnaphthalene acetic acid can also be obtained. Each step of the reaction requires attention to the activity of the reagent and the selectivity of the reaction, so as to achieve the purpose of efficient preparation. During the whole process of preparation, it is necessary to strictly control the conditions and monitor the progress of the reaction in order to obtain high-quality products.
What is the price range of 2,6-difluorophenylacetic acid in the market?
The price of 2% 2C6-diethylnaphthalene acetic acid in the market is difficult to determine. The price of the cover often changes due to various reasons, such as the trend of supply and demand, manufacturing costs, differences in quality and changes in market conditions.
Watching supply and demand, if there are many people who want it, but there are few people who supply it, the price will increase; conversely, if the supply exceeds demand, the price will decrease. Manufacturing costs are also a major factor. The price of raw materials, the number of labor costs, and the amount of energy consumption are all related to costs. If the cost increases, the selling price will also increase; if the cost decreases, the price may decrease.
The difference in quality also affects its price. Excellent quality, the price is always high; inferior quality, the price is low. And the market fluctuates, the rise and fall of the economy, changes in policies, and the presence of competing products can all make the price fluctuate.
To know the exact price, you should consult chemical raw material suppliers, distributors, or check the quotation of chemical product trading platforms. However, this price is only a temporary number, not constant. Or between a few yuan per gram and a few tens of yuan per gram, it is difficult to determine the exact value. Those who buy this product can get the right price only when they are widely inspected and consulted.