2 4 Difluoro 1h 1 2 4 Triazol 1 Yl Acetophenone Hydrochloride
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
2,4-difluoro-α-(1H-1,2,4-triazol-1-yl)acetophenone hydrochloride
Chemical Formula C10H7ClF2N4O·HCl
Molecular Weight 307.10 g/mol
Physical State Solid at standard conditions
Solubility In Water Unknown without specific data
Solubility In Organic Solvents Unknown without specific data
Chemical Class Aryl triazole derivative
Chemical Name 2,4 - difluoro - α - (1H - 1,2,4 - triazol - 1 - yl)acetophenone hydrochloride
Molecular Formula C10H7F2N3O·HCl
Molecular Weight 261.64 (approximate, considering addition of HCl to the base molecule)
Appearance Typically a solid (crystalline powder in many cases)
Physical State Solid at room temperature
Solubility Solubility characteristics vary; may be sparingly soluble in water, more soluble in certain organic solvents like polar aprotic solvents
Melting Point Specific melting point would need to be experimentally determined but would be characteristic of this compound
Purity Can be produced in various purity levels, e.g., 95%, 98% etc., depending on synthesis and purification methods
Odor Likely odorless or with a very faint, characteristic odor
Stability Stable under normal storage conditions; may be sensitive to heat, light, and moisture to some extent
FAQ

What is the chemical structure of 2,4-difluoro-alpha - (1H-1,2,4-triazole-1-yl) acetophenone hydrochloride?

This is the chemical structure analysis of 2,4-diene - α - ( 1H-1,2,4-triazole-1-yl) benzyl ketoxime. Its structure is quite complex and consists of a delicate combination of several parts.

The first is the 2,4-diene part, which is a structural fragment containing two carbon-carbon double bonds, which endows the compound with specific unsaturation and reactivity. Double bonds are highly reactive functional groups in organic chemistry, which can participate in many reactions such as addition and oxidation, and have a profound impact on the chemical properties of compounds. The order of

is the alpha - (1H - 1,2,4 - triazole - 1 - base) part, and the 1,2,4 - triazole ring is a five-membered heterocyclic ring with a unique distribution of nitrogen atoms in the ring. This heterocyclic ring has certain aromaticity, and due to the electronegativity of nitrogen atoms, the ring presents a specific electron cloud distribution. It can be combined with other molecules through weak interactions such as hydrogen bond 、π - π accumulation, which is of great significance in drug design, coordination chemistry and other fields. It is connected to the alpha site and precisely localized, which has an impact on the spatial orientation of the overall structure and electronic effects. < Br >
In addition, the oxime moiety of benzyl ketoxime, benzyl is benzyl, with the stability and certain hydrophobicity of benzene ring. In the oxime structure of ketoxime, ketoxime is formed by the reaction of ketone and hydroxylamine, while the acid oxime part contains acidic functional groups. Such structures can be used as key intermediates in organic synthesis, and may also impart specific biological activities to compounds, such as interacting with specific targets in organisms or participating in physiological processes related to acid-base balance.

In summary, the chemical structure of 2,4-diene - α - ( 1H-1,2,4-triazole-1-yl) benzylketoxime is cleverly spliced by the above multi-component structure, and the synergistic effect of each part endows the compound with unique physical, chemical and biological properties, which may have potential application value in organic synthesis, drug development and other fields.

What are the main uses of 2,4-difluoro-alpha - (1H-1,2,4-triazole-1-yl) acetophenone hydrochloride?

2% 2C4-diene - α - ( 1H - 1% 2C2% 2C4-triazole-1-yl) benzyl ketoglutaric anhydride, this is a complex organic compound. It is widely used in the field of pesticides and is often used as a key intermediate in the creation of fungicides. Because its structure contains triazole groups, it shows significant inhibitory activity against many plant pathogens, helping crops resist disease attack and improve yield and quality.

In the field of pharmaceutical research, this compound also has potential value. Scientists speculate that it may have specific biological activities, such as targeting certain disease-related targets, and can be used as a lead compound for in-depth research. After structural modification and optimization, it is expected to develop new therapeutic drugs.

In the field of organic synthesis, it acts as an important synthetic building block. With its unique structure, it can participate in many organic reactions and build more complex organic molecular structures, laying the foundation for the synthesis of new functional materials and other high-value-added organic compounds.

Looking at this compound, as "Tiangong Kaiwu" said: "Everything in the world has its uses. If you make good use of it, you can benefit people." Although this compound has a complex structure, it has been studied and applied by human wisdom, and has played important roles in many fields such as pesticides, medicine, and organic synthesis, contributing to human life and technological development.

What is the synthesis method of 2,4-difluoro-alpha - (1H-1,2,4-triazole-1-yl) acetophenone hydrochloride?

To prepare 2,4-diene - α - ( 1H-1,2,4-triazole-1-yl) benzyl ketoglutaric anhydride, the method is as follows:
First take an appropriate amount of starting materials and carefully prepare the ratio. Usually start with a specific organic compound, or a substrate containing alkenyl, triazolyl, benzyl ketone and diacid anhydride related structures as the starting point.
At the beginning of the reaction, a specific reaction environment is often required, or under an inert gas atmosphere, to prevent side reactions between the raw materials and products and the components in the air. Choose an appropriate solvent, such as some halogenated hydrocarbons, ethers or amide solvents, to help the raw materials mix evenly and facilitate the reaction. In the
reaction process, catalysts are indispensable. Or metal salt catalysts, such as copper salts, palladium salts, etc., use their catalytic activity to promote specific chemical reactions between groups, such as coupling reactions, cyclization reactions, etc., to build the backbone of the target molecule.
The reaction conditions also need to be finely regulated, and the temperature and time are all related to the success or failure of the reaction. The temperature may be maintained at a certain range, depending on the reaction process and the characteristics of the target product, or it may be initiated at low temperature and gradually heated to accelerate the reaction. The time also needs to be precisely controlled. If it is too short, the reaction will not be completed, and if it is too long, side reactions will breed.
After the reaction is completed, the pure 2,4-diene - α - ( 1H-1,2,4-triazole-1-yl) benzyl ketoglutaric anhydride product is obtained by conventional separation and purification methods, such as column chromatography, recrystallization, etc. During the operation, strict chemical experimental specifications must be followed to ensure the safety of the experiment and the accuracy of the results.

What are the physical and chemical properties of 2,4-difluoro-alpha - (1H-1,2,4-triazole-1-yl) acetophenone hydrochloride?

2% 2C4-diene - α - ( 1H-1% 2C2% 2C4-triazole-1-yl) benzyl ketone glutarate ketone, which is a member of the field of organic compounds. Its physical and chemical properties are rich and unique, which is of great significance to chemical research and related applications.

Looking at its physical properties, under normal circumstances, this compound may be in solid form, but the exact state is affected by factors such as intermolecular forces and crystal structure. Its melting point and boiling point are key indicators. The melting point characterizes the temperature at which a substance changes from solid to liquid state, and the boiling point is the temperature at which it converts from liquid to gaseous state. Both are indispensable in the separation, purification and identification of substances. In terms of solubility, it shows different performances in different solvents, with a certain solubility in polar solvents such as methanol and ethanol, or due to the formation of hydrogen bonds or other interactions with solvent molecules; in non-polar solvents such as n-hexane and benzene, the solubility may be limited due to molecular polarity differences.

Regarding chemical properties, the compound contains 2,4-diene structure, rich in π electrons, with high reactivity, prone to addition reactions, such as reacting with electrophilic reagents, electrophilic reagents attack double bonds and form new chemical bonds. This reaction provides an effective way to construct complex organic molecular structures. The structure of α - (1H - 1,2,4 - triazole - 1 - yl) benzyl ketone cannot be ignored either. The triazole ring has a unique electronic effect, which affects the electron cloud density of the groups connected to it, and then affects the reactivity and selectivity of the compound. And the carbonyl group is an active functional group, which can undergo nucleophilic addition reaction. Many nucleophilic reagents such as alcohols and amines can react with it, and a variety of compounds can be derived, which are widely used in the field of organic synthesis. The ketone glutarate structure gives compounds a certain acidity. Under specific conditions, acid-base reactions can occur and participate in various chemical transformation processes.

In summary, the physical and chemical properties of 2% 2C4-diene - α - ( 1H-1% 2C2% 2C4-triazole-1-yl) benzyl ketone glutarate ketone are rich and diverse, which lays a solid foundation for research and application in organic synthesis, medicinal chemistry and other fields.

What is the market availability of 2,4-difluoro-alpha - (1H-1,2,4-triazole-1-yl) acetophenone hydrochloride?

In today's world, there are many and complex goods in the city. If you want to know the supply and demand situation of 2,4-diene - α - ( 1H-1,2,4-triazole-1-yl) benzyl ketoglutaric acid, you need to explore it in many ways.

Looking for various pharmaceutical workshops, this product may be involved in the field of pharmaceutical and chemical industry, and its supply situation is often dependent on many factors. The production industry of watchers, if they are skilled, well-equipped and the raw materials are safe, the production capacity may be stable. However, the procurement of raw materials is often disturbed by weather, origin decrees, and supply and demand games in the city. If the weather is not good, the harvest of the raw material production area is not abundant, or the government order changes suddenly, restricting the circulation, the production will be blocked, and the supply will also shrink.

As for the demand side, the progress of pharmaceutical research and development and the expansion of clinical application are the keys to affecting demand. If a new drug is created, it needs to be based on this product, or the efficacy of existing drugs is praised, and the dosage surges, the demand will rise. On the contrary, if research and development is hindered, or there are alternatives in the world, the demand may decline.

From the current perspective, the supply of this product in the market, or due to various variables in production, fluctuates. Sometimes it is abundant, because the production is smooth, the raw materials are sufficient, and the factories compete for production; sometimes it is tight, because the raw materials are scarce and the production is twisted. The change in demand also moves with the tide of the pharmaceutical industry. The advent of new drugs and the rise and fall of old drugs can make them rise and fall.

Therefore, in order to clarify the certainty of supply and demand for this product, when the industry information is widely collected and the production flow and demand changes are carefully observed, the details can be obtained and the situation can be understood in order to respond to various changes in the city.