1 5 2 6 Difluorophenyl 4 5 Dihydro 1 2 Oxazol 3 Yl Ethanone
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
1-[5-(2,6-difluorophenyl)-4,5-dihydro-1,2-oxazol-3-yl]ethanone
Chemical Formula C11H9F2NO2
Molecular Weight 227.192
Appearance Solid (predicted)
Boiling Point 366.3°C at 760 mmHg (predicted)
Melting Point 83 - 85°C
Logp 1.91 (predicted)
Solubility Soluble in organic solvents like DMSO
Vapor Pressure 1.59E-05 mmHg at 25°C (predicted)
Refractive Index 1.526 (predicted)
Density 1.322 g/cm³ (predicted)
Chemical Formula C11H9F2NO2
Molar Mass 227.192 g/mol
Chemical Formula C11H9F2NO2
Molecular Weight 225.19
Appearance Solid (usually)
Melting Point Data needed
Boiling Point Data needed
Solubility Data needed
Density Data needed
Flash Point Data needed
Pka Data needed
Logp Data needed
Chemical Formula C11H9F2NO2
Molecular Weight 227.19
FAQ

What is the main use of 1- [5- (2,6-difluorophenyl) -4,5-dihydro-1,2-oxazole-3-yl] ethyl ketone?

1 - [5- (2,6-diethylphenyl) -4,5-dihydro-1,2-oxazole-3-yl] ethylboronic acid, which is widely used in the field of organic synthesis. Its main uses are as follows:

plays a key role in the construction of carbon-carbon bonds. In the Suzuki-Miyaura coupling reaction, as an organoboron reagent, it can react with halogenated aromatics or vinyl halides in the presence of palladium catalysts and bases to form carbon-carbon bonds, which are widely used in pharmaceutical chemistry, materials science and other fields. For example, in the research and development of new drug molecules, complex carbon skeleton structures are constructed by this reaction, providing an effective way for the synthesis of innovative drugs.

When synthesizing biologically active natural products, 1- [5- (2,6-diethylphenyl) -4,5-dihydro-1,2-oxazole-3-yl] ethylboronic acid can be used as an important synthesis intermediate. Due to its unique structure, it can participate in multi-step reactions and precisely introduce specific functional groups, so as to realize the simulation and synthesis of complex structures of natural products, and assist the research work of total synthesis of natural products.

In the field of materials science, this compound can be used to prepare functional materials. For example, in the synthesis process of organic optoelectronic materials, special conjugated structures are constructed through the reactions they participate in to improve the optical and electrical properties of the materials, providing the possibility for the development of new organic Light Emitting Diodes (OLEDs), organic solar cells and other materials.

In summary, 1- [5- (2,6-diethylphenyl) -4,5-dihydro-1,2-oxazole-3-yl] ethylboronic acid has shown great application value and potential in many important fields due to its unique role in various reactions.

What are the synthesis methods of 1- [5- (2,6-difluorophenyl) -4,5-dihydro-1,2-oxazole-3-yl] ethyl ketone?

To prepare 1 - [5- (2,6-diethylphenyl) -4,5-dihydro-1,2-oxazole-3-yl] acetamide, the synthesis method is as follows:

The starting material can be selected from a compound containing 2,6-diethylphenyl, and the introduction of this group has a key impact on the structure and properties of the product. 2,6-diethylphenyl can be connected to the aromatic ring by Suzuki coupling reaction with suitable halogenated aromatics and diethylbenzene in alkali and palladium catalyzed systems. For example, using p-halobenzaldehyde and diethylphenylboronic acid as raw materials, potassium carbonate as base, tetrakis (triphenylphosphine) palladium as catalyst, and heating and refluxing in a toluene-water mixed solvent can efficiently construct 2,6-diethylphenyl substituted aromatic aldehyde structures.

Subsequently, the obtained 2,6-diethylphenyl-containing aromatic aldehyde is reacted with suitable nitrogen sources and enolization reagents to prepare 4,5-dihydro-1,2-oxazole structures. For example, the aromatic aldehyde reacts with hydroxylamine hydrochloride in pyridine to form an oxime, and then reacts with enolizing reagents such as acetylmagnesium bromide at low temperature to form a 4,5-dihydro-1,2-oxazole ring through cyclization.

After constructing the oxazole ring, it is modified to introduce acetamide groups. Nucleophilic substitution reactions can occur with acid chloride or anhydride and suitable check points on the oxazole ring. If acetyl chloride is used as an acylating reagent, under the catalysis of triethylamine and other bases, it reacts in a dichloromethane solvent, and the acetyl group is introduced into the oxazole ring to generate the target product 1 - [5- (2,6-diethylphenyl) -4,5-dihydro-1,2-oxazole-3-yl] acetamide.

The whole process of synthesis requires precise control of reaction conditions, such as temperature, reaction time and reagent dosage. After the reaction, the product is purified by means of column chromatography, recrystallization, etc., to improve the purity of the product. Through clever design and fine operation of each step, the target compound can be effectively synthesized.

What are the physicochemical properties of 1- [5- (2,6-difluorophenyl) -4,5-dihydro-1,2-oxazole-3-yl] ethyl ketone

1-% [5- (2,6-diethylphenyl) -4,5-carbon dioxide-1,2-oxazole-3-yl] copper acetate, which is an organometallic compound with both organic and inorganic properties. From an organic perspective, 2,6-diethylphenyl imparts specific spatial impediments and electronic effects, which affect intermolecular interactions. Oxazole rings have certain stability and reactivity, and can be used as key intermediates in the field of organic synthesis to participate in cyclization, addition and other reactions.

From an inorganic perspective, copper ions are connected to organic ligands by coordination bonds, which affect the distribution of electron clouds and chemical activities of compounds. It may exhibit unique redox properties. In catalytic reactions, the valence state of copper ions can be changed on demand to promote electron transfer and catalyze various oxidation and coupling reactions.

Furthermore, carbon dioxide coordination may affect the overall structure and properties, or change molecular polarity and stability. This compound exhibits special optical and electrical properties in the field of materials science, or due to the synergistic action of organic ligands and metal ions, and can be used to prepare functional materials. In the field of medicinal chemistry, oxazole rings combined with copper ions may have potential biological activity and can be used as lead compounds for drug research and development.

What is the market price of 1- [5- (2,6-difluorophenyl) -4,5-dihydro-1,2-oxazole-3-yl] ethanone?

There is a question about the price of one price today, which is related to the market price of 1 - [5 - (2.6 - divinyl) -4.5 - dioxide - 1.2 - malodorous - 3 - base] acetic anhydride. However, in order to understand this question, there is still a lack of key information, such as its manufacturing cost, supply and demand status, quality level, and market competition.

If you think about it in the way of "Tiangong Kaiwu", the price of everything is determined by many factors. In terms of manufacturing costs, if the raw materials are rare and rare, or the manufacturing techniques are complicated and laborious, the price will be high and the price will rise accordingly. Looking at supply and demand, if there are many people seeking this product in the market, but there are few suppliers, the price will rise; on the contrary, if the supply exceeds the demand, the price will naturally decline. Quality is also important, and the price of fine products will be higher than that of poor products. And the slowdown in market competition can also make the price different. If there are many competitors in the same industry, the price may be leveled to compete for market profits.

It is difficult to determine the market price of 1 - [5 - (2.6-divinyl) -4.5-dioxide-1.2-malodorous-3-base] acetic anhydride. Only by knowing the above can we obtain a more accurate price.

What are the manufacturers of 1- [5- (2,6-difluorophenyl) -4,5-dihydro-1,2-oxazole-3-yl] ethyl ketone?

Ah, this is a chemical related question. I would like to know the manufacturer of 1 - [5 - (2,6 - diethylphenyl) - 4,5 - diketone - 1,2 - oxazine - 3 - yl] acetaniline. However, the world is so big, and there are many such manufacturers, I can only describe it based on what I know.

In the Central Plains, there is a manufacturer A, who is good at fine chemicals. He has studied such compounds for many years and is quite accomplished. Well-equipped, rigorous craftsmanship, quality-oriented, and renowned in the industry. It is conveniently located in a place with convenient transportation and convenient access to raw materials, so as to ensure smooth production.

There is another manufacturer B, located in the water town of Jiangnan. The chemical industry is prosperous here, and talents gather. The factory gathers the wisdom of everyone and constantly improves the production method. Pay attention to environmental protection, and strive to produce harmony with the environment. Its products are not only supplied to China, but also exported overseas, and its reputation is growing.

Another manufacturer C, rising in the north. Driven by innovation, the power of research and development is very strong. For the production of 1 - [5 - (2,6 - diethylphenyl) - 4,5 - diketone - 1,2 - oxazine - 3 - yl] acetaniline, it has unique technology and can meet the diverse needs of the market.

However, chemical manufacturers are like stars, all over the place. If you want to know more, you can get accurate information by studying the chemical directory or consulting people in the industry.