Chemical Formula | C7H7FO |
Molar Mass | 126.13 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | 194 - 196 °C |
Density | 1.173 g/cm³ |
Solubility In Water | Slightly soluble |
Solubility In Organic Solvents | Soluble in many organic solvents like ethanol, ether |
Flash Point | 82 °C |
Odor | Characteristic aromatic odor |
Chemical Formula | C7H7FO |
Molar Mass | 126.13 g/mol |
Appearance | Colorless liquid |
Odor | Characteristic |
Density | 1.165 g/cm³ |
Boiling Point | 196 - 198 °C |
Solubility In Water | Slightly soluble |
Solubility In Organic Solvents | Soluble in common organic solvents |
Flash Point | 84 °C |
Logp | 1.34 |
What are the main uses of o-Fluorobenzyl alcohol?
O-Fluorobenzyl alcohol (o-Fluorobenzyl alcohol) is also an organic compound. It has a wide range of uses and is often a key raw material and intermediate in the field of organic synthesis.
First, in the process of drug synthesis, o-Fluorobenzyl alcohol can participate in the construction of many drug molecules. Taking some antibacterial and anti-inflammatory drugs as an example, the construction of its chemical structure often depends on o-Fluorobenzyl alcohol as the starting material. Through a series of chemical reactions, such as esterification, etherification, amidation, etc., complex molecules with specific pharmacological activities are gradually constructed. Due to the introduction of fluorine atoms, the physical and chemical properties of the compound such as electron cloud distribution and lipophilicity can be changed, thereby improving the bioavailability of the drug, enhancing the affinity with the target, and optimizing the therapeutic effect of the drug. < Br >
Second, in the field of materials science, o-fluorobenzyl alcohol can also be used. In the preparation of polymer materials, it can be used as a functional monomer to participate in the polymerization reaction. The synthesized polymer materials may have excellent corrosion resistance, low surface energy and other special properties due to the characteristics of fluorine atoms. For example, it is used to prepare special coating materials, applied to the surface of metals, ceramics, etc., which can protect the base material from chemical attack, and has the effect of hydrophobic and oil-repellent, enhancing the service life and application value of the material.
Third, in the synthesis of fragrances, o-fluorobenzyl alcohol can contribute unique odor characteristics. After proper chemical modification and preparation, fragrance compounds with special aromas can be prepared, which can be used in perfumes, cosmetics, food additives and other industries to add unique aroma styles to products and meet consumers' needs for different fragrances.
In short, o-fluorobenzyl alcohol plays an important role in organic synthesis, drugs, materials, fragrances and many other fields. With the advance of science and technology, its use may become more extensive, injecting new impetus into the development of various industries.
What are the physical properties of o-Fluorobenzyl alcohol?
O-Fluorobenzyl alcohol (o-Fluorobenzyl alcohol) is also an organic compound. Its physical properties are particularly important, and it is related to its performance in various chemical processes and industrial applications.
First of all, its appearance, o-Fluorobenzyl alcohol is generally colorless to light yellow transparent liquid at room temperature. It is clear in appearance and has no visible impurities. This state is convenient for it to mix and melt with other substances in various reaction systems and participate in the reaction smoothly.
As for its boiling point, it is about 207-208 ° C. The boiling point is the critical temperature at which a substance changes from liquid to gaseous state. This specific boiling point indicates that at the corresponding temperature, o-Fluorobenzyl alcohol can change from liquid phase to gas phase. Knowing this value is crucial in chemical operations such as distillation and separation. It can be used to accurately control temperature and achieve phase separation of substances with different boiling points.
In terms of melting point, the melting point of o-fluorobenzyl alcohol is about -30 ° C. The melting point is the temperature limit for the transformation of solid substances into liquid. Above this temperature, o-fluorobenzyl alcohol is composed of solid and liquid. This property needs to be taken into account when storing and setting specific reaction conditions.
Density is also one of its important physical properties, about 1.163g/mL (25 ° C). The density represents the mass of a unit volume of material, so that the quality of a certain volume of o-fluorobenzyl alcohol can be measured. It is indispensable for formulation and measurement.
In terms of solubility, o-fluorobenzyl alcohol is slightly soluble in water, but it can be miscible with many organic solvents, such as ethanol, ether, etc. This solubility characteristic makes it possible to choose an appropriate solvent system according to the reaction requirements in organic synthesis to promote the progress of the reaction or to facilitate the separation and purification of the product.
In addition, o-fluorobenzyl alcohol has a certain degree of volatility. Although it is not a very volatile substance, it will evaporate slowly in an exposed environment or under specific temperature conditions. This property should be noted when storing. It should be sealed and stored in a cool place to prevent it from dissipating and to avoid the risk of safety due to its increasing concentration in the air.
What are the chemical properties of o-Fluorobenzyl alcohol?
O-Fluorobenzyl alcohol (o-Fluorobenzyl alcohol) is also an organic compound. It is active and has the characteristics of both alcohols and benzyl fluorides.
Looking at its chemical activity, the hydroxyl group is an active group, which can involve many reactions. If co-heated with carboxylic acids, with the help of catalysts, esters can be formed. This reaction uses concentrated sulfuric acid as a catalyst. Under heating conditions, the hydroxyl group of o-fluorobenzyl alcohol condenses with the carboxyl group of carboxylic acids, and the ester is obtained by dehydration. This is a common method of esterification.
Furthermore, the hydroxyl group can be oxidized. Treated with a mild oxidizing agent, such as Sarit reagent (Collins reagent), o-fluorobenzyl alcohol can be converted into o-fluorobenzaldehyde, and this reaction is controllable and If a strong oxidant, such as potassium permanganate, is used, it may be oxidized to the carboxylic acid stage.
The carbon-fluorine bond at its benzyl position also has a certain activity. Although the carbon-fluorine bond is relatively stable, under certain conditions, such as strong nucleophiles and high temperatures, fluorine atoms can be replaced. Nucleophiles such as sodium alcohols and amines can attack benzyl carbons, and the fluoride ions leave to form new carbon-heteroatomic bond compounds.
Because of its fluorine atom, the molecule has a certain fat solubility and special electronic effects. This property affects its physical properties, such as melting point, boiling point and solubility. Compared with fluorine-free analogs, its fat solubility or increase, better solubility in organic solvents, and solubility in water may be different, due to the strong electronegativity of fluorine atoms, which affects molecular polarity. In short, o-fluorobenzyl alcohol has unique chemical properties and is widely used in the field of organic synthesis. It can be used as an intermediate to prepare various fluorine-containing organic compounds.
What are the synthesis methods of o-Fluorobenzyl alcohol?
The method of synthesizing o-Fluorobenzyl alcohol has been explored by many scholars in the past, and the common ones are described today.
First, o-fluorotoluene is used as the starting material, and it is halogenated by the side chain. If it reacts with bromine under light conditions, o-fluorobenzyl bromide can be obtained. After the nucleophilic substitution reaction, the halogen atom is replaced with a hydroxyl group. It is often treated with an aqueous solution of sodium hydroxide or potassium hydroxide and heated to obtain o-fluorobenzyl alcohol. In this process, the side chain halogenation requires light to initiate a free radical reaction. The temperature of the nucleophilic substitution step should be controlled moderately to avoid the growth of side reactions.
Second, fluorobenzoic acid is used as the raw material. First reduce it to o-fluorobenzyl alcohol. Lithium aluminum hydride (LiAlH) can be used as a reducing agent to react in an anhydrous organic solvent such as ether or tetrahydrofuran. LiAlH) has strong reducing properties, and the reaction needs to be carried out at low temperature and in an anhydrous environment to prevent it from reacting violently with water. After the reaction is completed, the excess reducing agent and the generated salt are removed by hydrolysis treatment, and then separated and purified to obtain pure o-fluorobenzyl alcohol.
Third, use o-fluorobenzaldehyde as a raw material. Using sodium borohydride (NaBH) as a reducing agent and reacting in an alcohol solvent such as methanol or ethanol, the aldehyde group can be reduced to a hydroxyl group to generate o-fluorobenzyl alcohol. Sodium borohydride is relatively mild, the reaction conditions are easier to control, the product selectivity is high, and the post-treatment is also relatively simple. The target product can be obtained by conventional separation operations such as distillation and extraction.
All synthesis methods have their own advantages and disadvantages, and they need to be selected according to the actual situation, such as the availability of raw materials, cost, product purity requirements, etc.
What is the price range of o-Fluorobenzyl alcohol on the market?
The price of o-Fluorobenzyl alcohol (o-fluorobenzyl alcohol) in the market is difficult to determine, and its price often changes with time, and it is related to many reasons.
Looking at the market conditions of the past, its price fluctuates differently. If the supply is full, the market supply is abundant, and the price may decrease. However, if there is a lack of raw materials, or the preparation techniques are changed, resulting in a loss of output, the price may rise. And the needs of the market and the competition of the same industry also have a significant impact on the price.
When the market is calm, the price is about [X1] yuan per kilogram to [X2] yuan. However, when raw materials are scarce, or the market demand increases sharply, the price has also jumped to more than [X3] yuan per kilogram. And if the preparation method is refined, the yield will increase greatly, and the market supply will increase greatly, the price may drop to about [X4] yuan per kilogram.
is to know the exact price, and when you carefully observe the current market conditions and consult various suppliers, you can get a near-real price. The market is volatile, and the price changes with the trend, so it is difficult to determine the price range.