N 2 4 3 Fluorobenzyl Oxy Benzyl L Alaninamide
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
N~2~-{4-[(3-fluorobenzyl)oxy]benzyl}-L-alaninamide
Chemical Formula C20H22FN3O2
Molecular Weight 357.407 g/mol
Iupac Name N-[(4-[(3-fluorophenyl)methoxy]phenyl)methyl]-2-amino-propanamide
Appearance Solid (predicted)
Boiling Point 544.2°C at 760 mmHg (predicted)
Melting Point 113 - 115°C
Logp 4.18 (predicted)
Solubility Poorly soluble in water (predicted)
Pka 15.34±0.46 (Predicted)
Flash Point 283°C (predicted)
Chemical Formula C21H22FN3O2
Molecular Weight 367.417 g/mol
FAQ

What is the chemical structure of N~ 2~ - {4- [ (3-fluorobenzyl) oxy] benzyl} -L-alaninamide?

This is a problem of naming organic compounds. To solve the chemical structure of this compound "N~ 2~ - {4- [ (3-fluorobenzyl) oxy] benzyl} -L-alaninamide", it is necessary to analyze it according to the naming rules of organic chemistry.

First, "L-alaninamide" indicates that the basic structure of this compound is L-alaninamide. Alaninamide is one of the amino groups of alanine linked to the amide group. "N~ 2~" means that the substituent is attached to the nitrogen atom of the amino group of the alanine residue in alaninamide.

Furthermore, "{4- [ (3-fluorobenzyl) oxy] benzyl}" is a large substituent. " Benzyl "is benzyl, which is benzyl. In this substituent, there is a 3-fluorobenzyl group (3-fluorobenzyl), which is connected to another benzyl group through an oxygen atom, and this complex benzyl structure is integrally connected to the nitrogen atom of alanine.

From this, it can be seen that the chemical structure of this compound is L-alanamide as the parent body, and a substituent composed of 4- (3-fluorobenzoxy) benzyl is connected to the nitrogen atom. Specifically depicted, the amino nitrogen atom of alanamide is connected to a 4- (3-fluorobenzoxy) benzyl group, of which the fluorine atom of 3-fluorobenzyl is located in the benzene ring No. 3, and is connected to another benzyl group through an oxygen atom. The alanine part of alanamide retains its own carboxylaminated structure. In this way, the chemical structure of this compound can be clarified.

What are the main physical properties of N~ 2~ - {4- [ (3-fluorobenzyl) oxy] benzyl} -L-alaninamide?

N~ 2~ - {4- [ (3-fluorobenzyl) oxy] benzyl} -L-alaninamide is an organic compound. This compound has several key physical properties.

Its appearance is often white to off-white solid powder, which is easy to store and handle. In terms of solubility, it has a certain solubility in common organic solvents such as dichloromethane, N, N-dimethylformamide (DMF), but it is difficult to dissolve in water. This solubility characteristic has a great impact on the field of organic synthesis and drug development, and needs to be taken into account when designing reaction routes and dosage forms.

Its melting point is within a specific range, but the exact value varies depending on the purity of the sample and the test conditions. As a key physical property, the melting point can not only be used to identify the purity of the compound, but also provide clues for the thermal stability of the compound. Generally speaking, the melting point of the compound is relatively high, suggesting that its intermolecular forces are strong.

Stability is quite stable under conventional conditions. However, if exposed to strong acids, strong bases or high temperature environments, chemical reactions may occur, causing structural changes. During storage and use, it is necessary to avoid contact with these conditions to maintain its chemical integrity.

The physical properties of this compound are of great significance in the fields of organic synthesis and medicinal chemistry. In organic synthesis, solubility helps to select a suitable reaction solvent, and melting point provides a reference for reaction temperature control. In medicinal chemistry, these properties are associated with drug absorption, distribution, metabolism, and excretion, which have a profound impact on the drug development process.

In what fields is N~ 2~ - {4- [ (3-fluorobenzyl) oxy] benzyl} -L-alaninamide used?

N~ 2~ - {4- [ (3-fluorobenzyl) oxy] benzyl} -L-alaninamide is an organic compound. Looking at its structure, it contains fluorobenzoxy, benzyl and alanine amides. This unique structure endows it with diverse potential applications.

In the field of medicine, it may have considerable prospects. Due to its particularity of structure, it may interact with specific targets in organisms. Or it can regulate the function of proteins by binding to specific proteins, and play a role in the treatment of diseases. For example, in the development of anti-tumor drugs, such compounds may interfere with the signal transduction pathway of tumor cells and inhibit the proliferation and metastasis of tumor cells, but further pharmacological experiments are needed to prove it. < Br >
In the field of materials science, it may also have applications. Diverse groups in its structure may participate in the synthesis and modification of materials. For example, in the preparation of polymer materials, this compound can be used as a monomer or modifier, which may change the physical and chemical properties of the material, such as solubility, mechanical properties, surface activity, etc., and then expand the application of the material in different fields, such as the preparation of membrane materials with special properties for separation and filtration.

Furthermore, in the field of organic synthetic chemistry, this compound can be used as an important intermediate. The complexity and diversity of its structure provide organic synthesis chemists with a rich reaction check point, which can carry out a series of organic reactions, construct more complex and specific organic molecules, and promote the development and innovation of organic synthesis chemistry.

What is the preparation method of N~ 2~ - {4- [ (3-fluorobenzyl) oxy] benzyl} -L-alaninamide?

To make N%7E2%7E-%7B4-%5B%283-fluorobenzyl%29oxy%5Dbenzyl%7D-L-alaninamide, you can do it as follows.

First take an appropriate amount of 3-fluorobenzyl alcohol, mix it with a solution containing 4-hydroxybenzaldehyde, promote it with an appropriate amount of alkaline catalyst, control the temperature in a suitable range, so that the two carry out nucleophilic substitution reaction. After time, 4 - [ (3-fluorobenzyl) oxy] benzaldehyde can be obtained.

Next, the product is dissolved with L-alanine methyl ester hydrochloride in a suitable organic solvent, add an appropriate amount of organic base, adjust it to an appropriate pH, and cause it to undergo a condensation reaction. After the reaction is completed, neutralize with acid solution, extract and separate to obtain the corresponding condensation product. < Br >
Then the condensation product is placed in an alcohol solution containing ammonia, heated to reflux, the ester group is aminolyzed, and converted into an amide group. The reaction is completed, the solvent is removed by reduced pressure distillation, and then purified by column chromatography to obtain a crude product.

Finally, recrystallization with a suitable solvent can obtain a pure N%7E2%7E-%7B4-%5B%283-fluorobenzyl%29oxy%5Dbenzyl%7D-L-alaninamide. The whole process, pay attention to the control of reaction conditions, such as temperature, pH and reaction time, and each step of separation and purification is also crucial, so that the best effect can be obtained.

What are the market prospects for N~ 2~ - {4- [ (3-fluorobenzyl) oxy] benzyl} -L-alaninamide?

N%7E2%7E-%7B4-%5B%283-fluorobenzyl%29oxy%5Dbenzyl%7D-L-alaninamide this substance, the prospect of the market is actually shared by the business community and researchers. This substance has a unique chemical structure, and it has unlimited potential in the fields of medicine and materials, so the prospect is quite promising.

In the field of medicine, due to its specific molecular structure, it may be able to exhibit excellent pharmacological activity. Or it can be used as a lead compound for new drugs. After careful research, it is expected to develop a good drug against difficult diseases. The current medical industry is hungry for innovative drugs. This compound may be able to respond to this trend and bring good news to patients. Its market space is extremely broad.

As for the field of materials, its special structure may endow materials with novel properties. If this structure is introduced into polymer materials, it can improve the physical and chemical properties of the material, such as enhancing the stability and flexibility of the material. With the advancement of science and technology, the demand for high-performance materials is increasing, and this compound may emerge in the material innovation and open up a new market world.

However, if you want to make it unhindered in the market, you also face many challenges. The research and development process requires exquisite skills and huge investment to ensure the efficient, environmentally friendly and economical synthesis process. And the market competition is fierce, and you need to compete with congeneric products. However, if you can make good use of its unique advantages and overcome difficulties, you will be able to occupy a place in the market, lead the new trend of the industry, and have a bright future.