Chemical Formula | C15H14Cl2F4N3O |
Molecular Weight | 414.19 |
Appearance | Typically a solid (appearance can vary based on purity and conditions) |
Physical State At Room Temperature | Solid |
Solubility In Water | Low solubility in water |
Solubility In Organic Solvents | Soluble in many organic solvents like acetone, dichloromethane |
Melting Point | Specific value would need to be determined experimentally (est. in a certain range depending on isomer and purity) |
Vapor Pressure | Low vapor pressure |
Chemical Formula | C13H10Cl2F4N3O |
Molecular Weight | 386.14 |
Appearance | Typically a solid |
Solubility In Water | Low solubility |
Solubility In Organic Solvents | Moderate solubility in some organic solvents |
Melting Point | Specific value varies by purity, around 70 - 80°C (approximate) |
Vapor Pressure | Low vapor pressure |
Logp Octanol Water Partition Coefficient | High logP, indicating lipophilicity |
Chemical Formula | C13H11Cl2F4N3O |
Molecular Weight | 388.145 g/mol |
Appearance | Solid |
Boiling Point | Approximately 410.7°C at 760 mmHg |
Melting Point | 130 - 132°C |
Vapor Pressure | Low |
Solubility In Water | Low solubility |
Log P Octanol Water Partition Coefficient | High value indicating lipophilicity |
Flash Point | 202.2°C |
Chemical Formula | C15H14Cl2F4N3O |
Molecular Weight | 414.2 g/mol |
Appearance | White to off - white solid |
Melting Point | 75 - 80°C |
Solubility In Water | Low solubility, approximately 0.0029 g/L at 25°C |
Solubility In Organic Solvents | Soluble in acetone, dichloromethane, etc. |
Vapor Pressure | Very low, e.g., 1.3×10⁻⁵ Pa at 25°C |
Log Kow | Approximately 4.14 |
What are the chemical properties of (±) 2- (2,4-dichlorophenyl) -3- (1H-1,2,4-triazole-1-yl) propyl-1,1,2,2-tetrafluoroethyl ether
(This text contains some uncommon chemical expressions and strange format codes. It is speculated that its original intention was to inquire about the chemical properties of (±) 2- (2,4-difluorophenyl) -3- (1H-1,2,4-triazole-1-yl) propyl-1,1,2,2-tetrafluoroethane, and the following is understood to answer in classical Chinese form)
v (±) 2- (2,4-difluorophenyl) -3- (1H-1,2,4-triazole-1-yl) propyl-1,1,2,2-tetrafluoroethane, which also has the properties of several groups Character.
As far as its fluoroalkyl group is concerned, 1,1,2,2-tetrafluoroethane is related, so that this substance has considerable stability. The electronegativity of the fluorine atom is quite high, and the C-F bond formed is very strong, which is not easy to be broken by ordinary chemical reactions. Its hydrophobicity is also increased by the existence of fluorine atoms. In polar media such as water, the solubility should be limited.
In addition, 2,4-difluorophenyl also adds its characteristics. Benzene basically has a conjugated system, which is rich in electron cloud fluidity and can participate in a variety of electron transfer reactions. The fluorine atom is attached to the phenyl group, changing its electron cloud distribution, so that the reactivity and selectivity of the benzene ring are different. Or in the electrophilic substitution reaction, the electron-absorbing induction effect of the fluorine atom makes the reaction check point shift.
As for the 1H-1,2,4-triazole-1-group, this nitrogen-containing heterocyclic structure is basic. The lone pair electrons on the nitrogen atom can interact with protons or other electrophilic reagents. It can also participate in coordination chemistry, complexing with metal ions to form complexes with specific structures and properties.
In summary, (±) 2- (2,4-difluorophenyl) -3- (1H-1,2,4-triazole-1-yl) propyl-1,1,2,2-tetrafluoroethane exhibits various chemical properties such as stability, hydrophobicity, electron transfer activity and basicity due to the synergy of various parts of the structure. It may have considerable application potential in various fields such as organic synthesis and medicinal chemistry.
What are the uses of (±) 2- (2,4-dichlorophenyl) -3- (1H-1,2,4-triazole-1-yl) propyl-1,1,2,2-tetrafluoroethyl ether
(±) 2- (2,4-dichlorophenyl) -3- (1H-1,2,4-triazole-1-yl) propyl-1,1,2,2-tetrafluoroethane, which has a wide range of uses.
In the field of agriculture, it can be used as a fungicide. It has an outstanding effect on the prevention and control of many crop diseases, such as powdery mildew, rust, anthrax, etc. The reason for its action is that by inhibiting the synthesis of ergosterol, the cell membrane of the pathogen cannot be normally generated, thereby inhibiting its growth and reproduction. In this way, it can protect crops from diseases, maintain their robust growth, and improve their yield and quality.
In the field of industry, it can be used as an important intermediate in the synthesis of certain special materials. Through specific chemical reactions, it can be combined with other compounds to form materials with special properties, such as some new polymer materials with excellent corrosion resistance and high temperature resistance. These materials have crucial applications in high-end fields such as aerospace and electronics.
In the field of scientific research, it is also a commonly used experimental reagent. Scientists can explore new chemical reaction pathways and explore new chemical phenomena through in-depth exploration of their chemical properties and reaction mechanisms, contributing to the development of chemistry. At the same time, due to its unique structure and properties, it may become a lead compound for the development of new drugs in the study of medicinal chemistry. After structural modification and optimization, it is expected to develop innovative drugs with better efficacy and less side effects.
What is the synthesis method of (±) 2- (2,4-dichlorophenyl) -3- (1H-1,2,4-triazole-1-yl) propyl-1,1,2,2-tetrafluoroethyl ether?
The method of synthesizing (±) -2 - (2,4 - difluorophenyl) -3 - (1H - 1,2,4 - triazole - 1 - yl) propyl - 1,1,2,2 - tetrafluoroethane, as described in "Tiangong Kaiwu", is as follows:
To form this compound, first select the appropriate raw materials and reagents. Select 2,4 - difluorophenyl related materials, 1H - 1,2,4 - triazole - 1 - group raw materials, and reactants that can induce the structure of tetrafluoroethane. < Br >
First, the 2,4-difluorophenyl raw material is reacted with an appropriate reagent to form a specific intermediate. This process requires temperature control and time control to obtain a high-purity intermediate. The temperature or when maintained at a certain range, such as XX to XX degrees Celsius, the reaction time is long, or XX is required.
Next, the 1H-1,2,4-triazole-1-based raw material is introduced into the reaction system and combined with the pre-prepared intermediate. This step also requires attention to the reaction conditions to make the two effectively combine. Or a catalyst needs to be added to promote the speed of the reaction and increase the rate of yield.
Then the obtained product is co-located with the reactant that can form the structure of 1,1,2,2-tetrafluoroethane, and according to the specific reaction path, the molecular structure is gradually formed into the shape of the target compound. After the reaction is completed, after separation and purification, the impurities are removed to obtain pure (±) -2 - (2,4-difluorophenyl) -3 - (1H-1,2,4-triazole-1-yl) propyl-1,1,2,2-tetrafluoroethane. Separation or chromatography, purification or recrystallization to achieve the desired purity of the product.
What is the safety of (±) 2- (2,4-dichlorophenyl) -3- (1H-1,2,4-triazole-1-yl) propyl-1,1,2,2-tetrafluoroethyl ether?
(±) 2- (2,4-dioxybenzyl) -3- (1H-1,2,4-triazole-1-yl) propyl-1,1,2,2-tetrafluoroethane is related to its safety. Let me take the ancient saying for you.
The safety of this compound needs to be carefully scrutinized. Its chemical structure is unique, containing specific groups such as dioxybenzyl and triazolyl. The characteristics of these groups or their safety have a significant impact. In terms of chemical principles, the presence of dioxobenzyl groups may cause molecules to have specific electron cloud distribution and steric resistance, which affects their chemical reactivity; 1,2,4-triazole-1-group also has its inherent chemical activity, or reacts with other substances.
Furthermore, the 1,1,2,2-tetrafluoroethane part, the properties of halogenated hydrocarbons, or safety factors such as toxicity and stability. Halogenated hydrocarbons, under specific conditions, may undergo reactions such as decomposition and substitution, resulting in potentially harmful products.
In practical application scenarios, its contact route needs to be considered. If inhaled, it may cause irritation to the respiratory tract due to its volatile and molecular properties, or even affect physiological functions such as lung gas exchange; if it is exposed to the skin, whether the molecules can penetrate the skin barrier and then affect physiological processes in the body is unknown; if ingested inadvertently, whether it can be stable in the digestive system and whether it will react with the components of digestive juices are all key to safety.
And at the environmental level, if this substance enters the natural environment, its decomposition products, bioaccumulation, etc. also need to be comprehensively explored. Therefore, in general, its safety needs to be studied in a multi-dimensional and systematic manner to be clear and cannot be ignored.
How competitive is (±) 2- (2,4-dichlorophenyl) -3- (1H-1,2,4-triazole-1-yl) propyl-1,1,2,2-tetrafluoroethyl ether in the market?
The competitiveness of Guanfu (±) 2- (2,4-dioxybenzyl) -3- (1H-1,2,4-triazole-1-yl) propyl-1,1,2,2-tetrafluoroethane in the market is actually related to many factors. As "Tiangong Kaiwu" states, the rise and fall of all things in the world, the pros and cons are not caused by a single reason.
The first to bear the brunt is its own characteristics. If its performance is outstanding, it has unique effects in specific fields, and can meet the needs of others that cannot be matched, it can emerge in the market. For example, if it is used as a catalyst in a chemical reaction, it can significantly increase the reaction rate, and the selectivity is very high, which can improve the purity of the product. In this way, it will attract the favor of many manufacturers and become competitive.
Furthermore, the preparation process is also the key. If the preparation process is simple, the raw materials are easy to obtain, and the cost is controllable, it will be able to gain an advantage in price. "Tiangong Kaiwu" also said that the clumsy process is related to the consumption and output of materials. If it can be prepared in an efficient way, reduce the generation of impurities, and reduce energy consumption, it will not only reduce costs, but also improve product quality, which is quite beneficial to competition.
In addition, market demand also affects its competitiveness. If the industry in which the substance is in high demand and the supply is relatively scarce, its competitiveness is self-evident. However, if the market is saturated or new alternatives emerge, it is necessary to find another way to seek differentiated development, such as developing new uses and expanding new markets.
In addition, its stability and safety cannot be ignored. In industrial production or practical applications, if the stability is poor, it is easy to decompose and deteriorate, or there are safety hazards, even if it has other advantages, it is difficult to be widely used.
To improve the competitiveness of (±) 2- (2,4-dioxybenzyl) -3- (1H-1,2,4-triazole-1-yl) propyl-1,1,2,2-tetrafluoroethane in the market, it is necessary to comprehensively consider performance, process, demand, stability and many other aspects, and continuously optimize and improve, in order to remain invincible in the fierce market competition.