Chemical Formula | C9H5FN4 |
Molecular Weight | 188.16 g/mol |
Appearance | Solid (usually white or off - white) |
Melting Point | Data may vary, needs experimental determination |
Boiling Point | Data may vary, needs experimental determination |
Solubility In Water | Low solubility, likely sparingly soluble |
Solubility In Organic Solvents | Soluble in some polar organic solvents like DMSO, DMF |
Density | Data may vary, needs experimental determination |
Pka | Relevant functional groups' pKa values: amino group pKa may be around 8 - 10 |
Logp | Calculated logP value may suggest moderate lipophilicity |
Stability | Stable under normal conditions, may react with strong oxidizing or reducing agents |
Chemical Formula | C9H5FN4 |
Appearance | Solid (predicted) |
Solubility In Water | Low (predicted) |
Logp | 1.34 (predicted) |
Chemical Formula | C9H5FN4 |
Molecular Weight | 188.166 g/mol |
Appearance | Solid (likely, based on similar compounds) |
Physical State At Room Temp | Solid |
Solubility In Water | Limited (due to hydrophobic groups) |
Solubility In Organic Solvents | May be soluble in common organic solvents like DMSO, DMF |
Chemical Formula | C9H5FN4 |
Molecular Weight | 188.16 |
Appearance | Solid (predicted) |
Solubility | Insoluble in water (predicted) |
What are the main application fields of 4- (3-amino-1,2,4-triazine-6-yl) -2-fluorobenzonitrile?
4 - (3 - hydroxy - 1,2,4 - triazine - 6 - yl) - 2 - chlorophenylacetamide, the main application fields of this substance are as follows:
In the field of medicine, because of its unique chemical structure, or with specific biological activity. Can be used as a pharmaceutical intermediate for the synthesis of antibacterial drugs. By virtue of the mechanism of action against specific pathogens, it interferes with the key physiological processes of pathogens, achieves antibacterial effect, and helps treat bacterial infections. For example, for Gram-positive and negative bacteria causing respiratory tract and digestive tract infections, through rational drug design and modification, drugs are developed based on them, or have good antibacterial activity and low toxic and side effects. < Br >
In the field of pesticides, it can be used to create new types of pesticides. It has inhibitory or killing effects on certain pests and pathogens. For example, by affecting the nervous system and respiratory system of insects, or destroying the cell wall and cell membrane synthesis of pathogens, it can control crop diseases and pests, improve crop yield and quality, and is environmentally friendly, with low residues and reduced impact on the ecological environment.
In the field of materials science, its special structure can endow materials with unique properties. It is used to prepare functional polymer materials, such as by copolymerizing with polymer monomers, so that polymer materials have antibacterial, antioxidant and other properties, expand the application range of materials, add them to food packaging materials, and prolong the shelf life of food; it is used to prepare coatings to improve the antibacterial and antifouling properties of coatings.
In the field of organic synthesis, it is an important intermediate in organic synthesis. Due to the multiple activity check points in the molecule, it can participate in a variety of organic reactions and construct complex organic compound structures. Through nucleophilic substitution, addition and other reactions, different functional groups are introduced to provide a basis for the synthesis of new organic compounds, help the development of organic synthesis chemistry, and develop more organic compounds with special properties and uses.
What are the synthesis methods of 4- (3-amino-1,2,4-triazine-6-yl) -2-fluorobenzonitrile?
To prepare 4- (3-amino-1,2,4-triazole-6-yl) -2-chlorophenylacetamide, the synthesis method is as follows:
The starting material can be selected from suitable chlorophenylacetonitrile derivatives and 3-amino-1,2,4-triazole-6-carboxylic acid or its active derivatives for reaction. First hydrolyze chlorophenylacetonitrile under basic conditions to convert the nitrile group into a carboxyl group to obtain chlorophenylacetic acid. For example, use sodium hydroxide aqueous solution as a base and react at an appropriate temperature for a certain period of time. This step requires attention to control the reaction temperature and the amount of base to prevent excessive hydrolysis or other side reactions.
Next, the obtained chlorophenylacetic acid is reacted with a suitable activation reagent to activate its carboxyl group, such as reacting with dichlorosulfoxide to form chlorophenylacetyl chloride. The reaction is usually carried out in an inert solvent such as dichloromethane. It is necessary to slowly add dichlorosulfoxide dropwise under low temperature conditions and stir it evenly to ensure that the reaction is sufficient and to avoid side reactions.
On the other hand, for 3-amino-1,2,4-triazole-6-carboxylic acids, the amino groups can be properly protected first to prevent the amino groups from participating in unnecessary reactions in subsequent reactions. Commonly used protective groups such as tert-butoxycarbonyl (Boc) are introduced by reacting with corresponding protective reagents under suitable reaction conditions. Then, the protected 3-amino-1,2,4-triazole-6-carboxylic acid is condensed with chlorophenylacetyl chloride in the presence of a base. The base can be selected from an organic base such as triethylamine, and the chlorophenylacetyl chloride is slowly added dropwise to the reaction system at low temperature, and the reaction is stirred for a period of time to form an amide bond.
After the reaction is completed, the protective group on the amino group is removed. For the Boc protective group, a dilute acid such as hydrochloric acid can be used to carry out the deprotection reaction under appropriate conditions, and finally the target product 4- (3-amino-1,2,4-triazole-6-yl) -2-chlorophenylacetamide can be obtained. After each step of the reaction, the product needs to be separated and purified by suitable separation and purification methods, such as extraction, column chromatography, etc., to ensure the smooth progress of the reaction and the purity of the product.
What are the physicochemical properties of 4- (3-amino-1,2,4-triazine-6-yl) -2-fluorobenzonitrile?
4- (3-hydroxy-1,2,4-triazine-6-yl) -2-chlorobenzylacetic acid is an organic compound, which may have applications in the chemical and pharmaceutical fields. To clarify its physical and chemical properties, let me explain in detail.
The appearance of this compound may be white to light yellow crystalline powder, with a specific melting point and boiling point. The melting point is the temperature at which a substance changes from solid to liquid state. Accurate determination of the melting point is essential to identify the purity of the compound. Its melting point may be within a certain range, which varies slightly according to the purity of the compound and the determination method. The boiling point is the temperature at which a liquid is converted into a gas. Under a specific pressure, the boiling point of the compound is also a fixed value. < Br >
In terms of solubility, it may have a certain solubility in common organic solvents such as ethanol and acetone, but its solubility in water may be limited. Due to the molecular structure of the compound containing hydrophobic groups, it is difficult to dissolve in water with strong polarity. However, under specific conditions, its solubility in water may be improved by means of solubilizers, changing the pH value of the solution, etc.
In terms of stability, under normal storage and use conditions, the compound may be relatively stable. In case of extreme conditions such as high temperature, strong acid, strong base or strong oxidant, or chemical reactions may occur to cause structural changes. For example, at high temperature, chemical bonds within the molecule may be broken or rearranged; in strong acid and strong base environments, functional groups such as hydroxyl groups and chlorine atoms may participate in the reaction.
In addition, the compound may be volatile. Although the volatility is not strong, it is exposed to air for a long time, or the mass is reduced due to volatilization. At the same time, its odor is weak, or it has a special chemical smell.
In short, the physical and chemical properties of 4- (3-hydroxy-1,2,4-triazine-6-yl) -2-chlorobenzylacetic acid are significantly affected by the structure and functional groups. Understanding these properties is of great significance for its synthesis, application and storage.
What is the price trend of 4- (3-amino-1,2,4-triazine-6-yl) -2-fluorobenzonitrile in the market?
Since modern times, there have been many commercial roads, and the market situation has changed rapidly. The price trend of 4- (3-hydroxy-1,2,4-triazine-6-yl) -2-chlorophenylacetamide in the market is the key to commercial affairs.
Watch this chemical, the price fluctuation is related to various factors. First, the balance between supply and demand. If the world needs this 4- (3-hydroxy-1,2,4-triazine-6-yl) -2-chlorophenylacetamide, and the production is small, the price will rise; on the contrary, if the supply exceeds the demand, the price should be suppressed.
Both, the price of raw materials is also the main reason. The system of this chemical requires all kinds of raw materials, and the price of raw materials is high, the cost of the system will increase, and its price in the market will also rise; if the price of raw materials falls, the cost will drop, and the price may decline.
The three, the guidance of the government and the rules of the market, also affect the price. If a company issues policies that are conducive to the production system, or regulates the orderly market, the price may change; if the government is strict and restricts its production system, the price will be subject to turbulence.
Furthermore, the advance of science and technology also affects the price. The introduction of new techniques may increase the yield and reduce the cost, and the price may drop as a result; however, if new techniques generate new demand, the price may also rise.
In summary, the market price of 4- (3-hydroxy-1,2,4-triazine-6-yl) -2-chlorophenylacetamide is not uniform, but is the result of the interaction of supply and demand, raw materials, government decrees, science and technology and other factors. Its price trend, or the rise and fall of the wave, changes with the change of the market. Businesspeople need to judge the situation and observe the micro-knowledge in order to get a glimpse of its price change, so as to meet the needs of business.
What are the manufacturers of 4- (3-amino-1,2,4-triazine-6-yl) -2-fluorobenzonitrile?
The manufacturer of 4- (3-amino-1,2,4-triazole-6-yl) -2-chlorophenylacetamide recorded in "Tiangong Kaiwu" has no direct corresponding record in the ancient books. Because "Tiangong Kaiwu" was written by Song Yingxing in the Ming Dynasty, when it was written, the production process of such chemically synthesized things had not yet come out.
"Tiangong Kaiwu" details many traditional skills, such as agricultural mulberry, hardware casting, ceramic firing, etc., which were all key areas of social production and life at that time. However, the organic compounds mentioned today belong to modern chemical synthesis products, with complex chemical structures and specific synthesis paths. Their production involves modern chemical industry systems, such as organic synthesis, catalytic reactions, separation and purification, and a series of advanced technologies.
To know the manufacturer of this compound, it is necessary to explore the channels such as modern chemical industry information, professional chemical databases, and chemical product trading platforms. Nowadays, the chemical industry is widely distributed, and many chemical companies have the ability to produce such fine chemicals. However, specific manufacturers need to be comprehensively screened according to various factors such as region, production scale, and product Quality Standards.