A Amino 4 Fluorobenzeneacetic Acid
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
a-Amino-4-fluorobenzeneacetic acid
Name a-Amino-4-fluorobenzeneacetic acid
Molecular Formula C8H8FNO2
Molecular Weight 169.153 g/mol
Appearance Solid (usually white or off - white powder)
Melting Point Typically in a certain temperature range (needs more specific data)
Solubility Solubility in water is relatively low, soluble in some organic solvents like DMSO
Pka Value related to its acidic - basic properties (specific value needed)
Density A certain value (data required)
Name α -Amino-4-fluorobenzeneacetic acid
Chemical Formula C8H8FNO2
Molar Mass 169.15 g/mol
Appearance Solid
Solubility In Water Slightly soluble
Chemical Formula C8H8FNO2
Molar Mass 169.153 g/mol
Appearance Solid
Melting Point Data needed
Boiling Point Data needed
Density Data needed
Solubility In Water Data needed
Pka Data needed
Logp Data needed
Flash Point Data needed
FAQ

What is the chemistry of a-Amino-4-fluorobenzeneacetic acid?

A-Amino-4-fluorophenylacetic acid, this is an organic compound with unique chemical properties. It is in the form of a white to off-white crystalline powder and is quite stable under conventional conditions.

In terms of physical properties, the melting point of this substance is within a certain range, and the specific value varies slightly due to factors such as purity. It is slightly soluble in water, but soluble in many organic solvents, such as ethanol, ether, etc. This solubility allows it to react in suitable solvent systems in organic synthesis operations.

From chemical analysis, the amino group (-NH2O) in the molecule is alkaline and can react with acids to generate corresponding salts. The carboxyl group (-COOH) is acidic, can neutralize with bases, and can also participate in esterification reactions, forming esters with alcohols under specific conditions. The fluorine atom on the benzene ring, because of its high electronegativity, affects the distribution of the electron cloud of the benzene ring, resulting in changes in the properties of the benzene ring, which in turn affects the reactivity of the whole molecule. For example, it will reduce the density of the electron cloud at the o-para position of the benzene ring, and the electrophilic substitution reaction activity will change compared with benzene, and it is more inclined to meta-substitution. This substance is widely used in the field of organic synthesis and can be used as a key intermediate for the preparation of a variety of fine chemicals such as drugs and pesticides.

What are the main uses of a-Amino-4-fluorobenzeneacetic acid?

A-amino-4-fluorophenylacetic acid, which has a wide range of uses. In the field of pharmaceutical chemistry, it is a key organic synthesis raw material. It can be used to create many new drugs, because fluorinated organic compounds often have unique physiological activities, which can effectively improve the efficacy of drugs, enhance stability, and reduce toxic and side effects. Taking the development of anti-cancer drugs as an example, compounds containing this structure may be able to precisely act on specific targets of cancer cells and inhibit their growth and spread.

In pesticide chemistry, a-amino-4-fluorophenylacetic acid is also indispensable. After clever design and synthesis, high-efficiency and low-toxicity pesticides can be prepared. The introduction of fluorine atoms can enhance the biological activity of pesticides against pests and pathogens, improve their environmental stability and shelf life, reduce the frequency of application, reduce the impact on the environment, and help the sustainable development of agriculture.

In addition, in the field of materials science, it may participate in the synthesis of special materials. For example, the introduction of some functional polymer materials, a-amino-4-fluorophenylacetic acid as a structural unit, can endow materials with unique physical and chemical properties, such as improving material solubility, thermal stability and mechanical properties, and then broaden the application range of materials, playing an important role in cutting-edge fields such as electronics and optics.

What is the production method of a-Amino-4-fluorobenzeneacetic acid?

The method of making a-amino-4-fluorophenylacetic acid has been around for a long time. It is often started with 4-fluorophenylacetone, and it is first reacted with hydroxylamine hydrochloride and sodium acetate by oximization. Under appropriate temperature and pressure, the reaction process can be controlled to obtain 4-fluorophenylacetone oxime.

Then the oxime is rearranged with suitable reagents, such as phosphorus pentachloride or phosphorus oxychloride. This step also needs to pay attention to the temperature, reaction time and other conditions to make the rearrangement smooth and obtain 4-fluorophenylacetamide. After

, 4-fluorophenylacetamide is heated together with a strong base, such as sodium hydroxide, in water. This hydrolysis reaction, when appropriate, can obtain the sodium salt of a-amino-4-fluorophenylacetic acid. Finally, the pH value is adjusted with acid, crystallized, filtered, washed, dried, and finally pure a-amino-4-fluorophenylacetic acid is obtained.

Another method is to start with 4-fluorobenzaldehyde. This compound can also be prepared by condensation with malonic acid, etc., and then by multi-step reactions such as reduction and amination. However, each step of the reaction requires careful selection of reagents and good control of conditions in order to obtain high-yield and high-quality products. The equipment used should also be clean and combined, and the operation should be carried out according to regulations, in order to prepare a-amino-4-fluorophenylacetic acid.

What is the market outlook for a-Amino-4-fluorobenzeneacetic acid?

A-amino-4-fluorophenylacetic acid is a valuable compound in the field of organic synthesis. In the field of medicinal chemistry, as a key intermediate, it plays a pivotal role in the development of many drugs. Many drug molecules with specific pharmacological activities often use a-amino-4-fluorophenylacetic acid as the starting material or important structural fragment in their synthesis pathways.

Looking at its market prospects, with the vigorous development of the global pharmaceutical industry, the demand for various new drugs is increasing day by day. In view of the key position of a-amino-4-fluorophenylacetic acid in drug synthesis, its market demand has also increased steadily. Many pharmaceutical companies and scientific research institutions continue to increase the demand for this compound in order to develop innovative drugs.

Furthermore, in the field of fine chemicals, a-amino-4-fluorophenylacetic acid also shows certain application potential. It can be used to synthesize fine chemicals with special properties, such as the synthesis of some high-end coatings, functional materials, etc. With the technological progress and product upgrading of the fine chemical industry, the quality and yield requirements of a-amino-4-fluorophenylacetic acid are also more stringent.

However, there are also challenges in the market. On the one hand, the process of synthesizing a-amino-4-fluorophenylacetic acid needs to be continuously optimized to improve yield and reduce costs in order to gain an advantage in market competition. On the other hand, the stricter environmental protection requirements prompt the production process to comply with the concept of green chemistry, and put forward higher requirements for the environmental protection of the synthesis process. Overall, the market prospect of a-amino-4-fluorophenylacetic acid is promising, but it also needs to meet many challenges in order to achieve a sustainable and good development trend.

What are the precautions for a-Amino-4-fluorobenzeneacetic acid during storage and transportation?

A-Amino-4-fluorophenylacetic acid is also an organic compound. When storing and transporting, all kinds of precautions should not be ignored.

First words storage. This compound should be placed in a cool, dry and well-ventilated place. In a cool place, to prevent its properties from changing due to excessive temperature. If it is exposed to high temperature, or it may cause chemical changes, it will damage its quality. A dry environment is also the key. If it is covered or afraid of moisture, moisture will invade it, and reactions such as hydrolysis will damage its structure. Good ventilation can avoid the accumulation of harmful gases and maintain its chemical stability. And it needs to be stored separately from oxidizing agents, acids, alkalis, etc., because it coexists with them, or triggers violent chemical reactions, which may cause safety risks.

As for transportation, there are also many details. The packaging must be tight to ensure that there is no leakage on the way. Choose suitable packaging materials that can withstand certain external shocks and chemical erosion. When transporting, ensure that the vehicle runs smoothly and stops slowly to prevent vibration and collision from causing damage to the packaging. Transport personnel should also be familiar with its characteristics and can properly deal with emergencies. The means of transportation need to be clean and free of other chemicals left behind to avoid cross-contamination.

All of these are to be paid attention to when storing and transporting a-amino-4-fluorophenylacetic acid, so as to ensure its safety and quality.