4 4 Fluorobenzyloxy Phenylboronic Acid
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
4-(4'-FLUOROBENZYLOXY)PHENYLBORONIC ACID
Chemical Formula C13H12BO3F
Molecular Weight 246.04
Appearance Solid
Melting Point 135 - 139 °C
Boiling Point N/A
Density N/A
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Pka Value N/A
Flash Point N/A
Stability Stable under normal conditions, avoid strong oxidizing agents
Chemical Formula C13H12BO3F
Molecular Weight 246.04
Appearance Solid (Typical)
Cas Number 1217501-16-2
Purity Typically 97%+
Solubility In Common Solvents Soluble in organic solvents like dichloromethane, less in water
Melting Point N/A (depends on purity and measurement method)
Boiling Point N/A (decomposes before boiling typically)
Density N/A (no common values found)
Stability Stable under normal conditions, moisture - sensitive
FAQ

What are the main uses of 4- (4 '-fluorobenzoxy) phenylboronic acid?

4- (4 '-Hydroxyphenylacetamide) benzoic acid, also known as paracetamol impurity B, has important uses in the field of medicine.

This compound plays a key role in drug research and development. First, it is often used as an impurity reference substance. In the quality control of paracetamol and related drugs, accurate determination of the impurity content is crucial. During the production process of drugs, this impurity may be introduced due to factors such as raw material purity and reaction conditions. If its content exceeds the standard, it may affect the stability, efficacy, and even endanger the health of patients. Therefore, using 4- (4 '-hydroxyphenylacetamide) benzoic acid as an impurity reference substance will help pharmaceutical companies use high performance liquid chromatography and other analytical methods to accurately determine the impurity content in drugs and ensure the quality and safety of drugs.

Second, it is of great significance in the field of drug synthesis research. As an important intermediate, it can help researchers explore new synthesis routes and methods. Using it as a starting material, through chemical modification and reaction, novel compounds can be prepared, providing the possibility for the development of new antipyretic, analgesic and anti-inflammatory drugs. Developers hope that by modifying its structure, they can obtain drugs with better efficacy and fewer side effects, and promote the continuous progress of pharmaceutical science.

What are the synthesis methods of 4- (4 '-fluorobenzoxy) phenylboronic acid?

To prepare 4- (4 '-hydroxybutoxy) benzoic acid, the following ancient methods can be followed:

First take an appropriate amount of phenolic compounds, such as p-hydroxybenzoic acid, which is the starting material for the reaction. The activity of phenolic hydroxyl groups in its structure is crucial in subsequent reactions. Then take reagents containing hydroxybutoxy, such as 1,4-dibromobutane and alcohols. In an alkaline environment, the alcohol reacts with 1,4-dibromobutane first to form a halogen containing hydroxybutoxy. The function of a base is to capture the hydrogen of the hydroxyl group in the alcohol to form an alcohol negative ion, and then react with 1,4-dibromobutane for nucleophilic substitution.

Then, the resulting hydroxybutoxy halogen is mixed with p-hydroxybenzoic acid, placed in a suitable reaction system, and then an appropriate amount of alkali is added, such as potassium carbonate. The alkali prompts the phenolic hydroxyl group of p-hydroxybenzoic acid to form a phenoxy anion. This anion has strong nucleophilicity and launches a nucleophilic attack on the carbon position of the halogen atom containing the hydroxybutoxy halogen. The halogen atom leaves, thus forming the skeleton structure of 4- (4 '-hydroxybutoxy) benzoic acid. The reaction needs to be carried out at an appropriate temperature and duration to ensure the adequacy and efficiency of the reaction.

Or another method may be used, first using p-hydroxybenzoic acid as a group to properly protect its carboxyl group, such as converting it into an ester group. In this way, the carboxyl group can be avoided from being affected in the subsequent reaction. Then, the p-hydroxybenzoic acid after protecting the carboxyl group is reacted with the hydroxybutoxy-containing reagent according to the above method of nucleophilic substitution. After the desired ether bond structure is formed, the protective group of the carboxyl group is removed and the carboxyl group is restored by means of hydrolysis, etc., to obtain 4- (4 '-hydroxybutoxy) benzoic acid. In this process, the protection and deprotection steps need to be carefully operated, and the reagents and conditions used need to be precisely controlled to obtain the ideal product.

What are the physical properties of 4- (4 '-fluorobenzoxy) phenylboronic acid?

4 - (4 '-Hydroxyethyl) pyridinecarboxylic acid, an organic compound. Its physical properties are as follows:
1. ** Appearance **: At room temperature, it is usually white to light yellow crystalline powder with fine texture, pure appearance, and no variegation and foreign matter. This form is convenient for storage, transportation and subsequent processing. Due to its stable state, it is not prone to significant physical changes in general environments.
2. ** Melting point **: Has a specific melting point, about 140-145 ° C. The melting point is an important physical property of the compound. This temperature range indicates that it will change from solid to liquid in this zone. Precise melting point can be used for purity identification. If the purity is high, the melting point range is narrow and close to the theoretical value; if it contains impurities, the melting point is reduced and the range is widened.
3. ** Solubility **: It has a certain solubility in water and can partially dissolve to form a uniform solution. It has better solubility in polar organic solvents such as ethanol and methanol, and can be well miscible with these solvents. This solubility is related to polar groups in the molecular structure, which makes it have different solubility behaviors in different solvent environments, laying the foundation for its application in various chemical reactions and preparation preparations.
4. ** Odor and Taste **: The smell is weak, and there is almost no special odor emission. It tastes odorless, which makes it advantageous in some application scenarios that are sensitive to odor and taste, and will not interfere with the original odor and taste of the system.
5. ** Stability **: Under normal storage and use conditions, the chemical properties are stable, and it is not easy to spontaneously decompose and oxidize. However, in extreme chemical environments such as strong oxidants, strong acids, and strong bases, the structure may be damaged and chemical reactions occur. When storing, avoid contact with such substances and place in a cool, dry, and well-ventilated place to maintain its physical and chemical stability.

What should be paid attention to when storing 4- (4 '-fluorobenzoxy) phenylboronic acid?

4 - (4 '-Hydroxyphenoxy) benzaldehyde, this substance should pay attention to the following matters when storing:

First, pay attention to the temperature and humidity of the environment. Due to its nature or deterioration due to temperature and humidity, it should be stored in a place with relatively constant temperature and suitable humidity. Generally speaking, the temperature should be controlled below 25 ° C, and the humidity should be maintained at 60% - 70%. In this way, it can effectively slow down the chemical changes caused by temperature and humidity changes and ensure the stability of its chemical structure.

Second, pay attention to isolating the air. The substance may oxidize with oxygen in the air, which will affect its quality. Therefore, the storage container should have good sealing, and can be filled with inert gases such as nitrogen to replace air, creating an oxygen-free environment, thereby reducing the risk of oxidation.

Third, avoid light. Light or lead to luminescent chemical reactions, causing the substance to decompose or undergo other adverse changes. Therefore, it should be stored in a dark place, such as in a brown bottle or stored in a dark place, to block the effect of light on it.

Fourth, the storage place should be away from fire sources, heat sources and strong oxidants. This substance may be flammable, close to fire sources and heat sources are prone to fire; and strong oxidants can react violently with it, endangering storage safety.

Fifth, it should be stored separately from other chemicals. Different chemicals have different properties, and mixed storage or chemical reactions can lead to danger. Be sure to store them properly according to their chemical properties to ensure the safety and stability of the storage process.

What is the market price of 4- (4 '-fluorobenzoxy) phenylboronic acid?

In today's world, in the market, the price of 4- (4 '-hydroxyethyl) quinoline carboxylic acid often varies due to various reasons.

First, it is related to the quality of this drug. If the quality is high and pure, it meets all the strict regulations, and it is a good choice for pharmaceuticals, the price is often high. And the quality is inferior, and there are many impurities, which hinders the use, and the price is low.

Second, the supply and demand of the city is also the main reason. If there are many drug companies, but there are few producers, the demand is greater than the supply, and the price will rise. On the contrary, if the supply exceeds the demand, the price will decline.

Third, the cost of the system also affects the price. The price of raw materials, the cost of manpower, and the simplicity of the craftsmanship all have an impact. If raw materials are rare, the craftsmanship is complicated, and the cost is high, the price will also be higher.

Fourth, the distance of the place also affects the price. Long-distance transportation costs a lot, and when it arrives at the place of sale, the price may increase.

Fifth, changes in government decrees and regulations can also affect the price. For example, tax changes and strict regulations can affect the price.

In summary, the market price of 4- (4 '-hydroxyethyl) quinoline carboxylic acid is not constant, but changes with the movement of various factors. Whether it is high or low, it is difficult to determine the number. It takes time to observe it before we can know the truth of its market conditions.