2-Aminosulfonyl-3-(2,2,2-trifluoroethoxy)pyridine

2-Aminosulfonyl-3- (2,2,2-trifluoroethoxy) pyridine is one of the organic compounds. Its main uses are more common in the fields of medicine, pesticides and materials science.
In the field of medicine, this compound is often used as a key intermediate for the synthesis of biologically active drug molecules. Due to its unique chemical structure, it can endow drugs with specific pharmacological properties. For example, it may enhance the affinity of the drug to the target, improve the efficacy of the drug; or improve the pharmacokinetic properties and prolong the action time of the drug in vivo.
In the field of pesticides, 2-aminosulfonyl-3- (2,2,2-trifluoroethoxy) pyridine is also an important synthetic raw material. By modifying its structure, new and efficient pesticides can be created for the prevention and control of pests and diseases. Because of its fluorine-containing group, it may make the pesticide have better lipid solubility and stability, and it is easier to penetrate the epidermis of pests or the stratum corneum of plants, enhancing the efficacy.
In materials science, this compound can participate in the synthesis of functional materials. Such as the synthesis of materials with special optical, electrical or thermal properties. The sulfonyl group and fluoroethoxy group in its structure can have a significant impact on the properties of materials, or improve the heat resistance and chemical stability of materials, or endow materials with unique optical properties, such as fluorescence properties.
In summary, 2-aminosulfonyl-3- (2,2,2-trifluoroethoxy) pyridine has key uses in many important fields, and is of great significance to promote technological development and innovation in related fields.

The synthesis method of 2-aminosulfonyl-3- (2,2,2-trifluoroethoxy) pyridine is the way to go.
First, the compound containing pyridine can be produced, and the aminosulfonyl group can be introduced into the aminosulfonyl group. In this step, the sulfonyl chloride derivative can be used, as in the environment, with the nitrogen atom of the pyridine as the nucleus, and the sulfonyl chloride can be reacted to form the aminosulfonyl pyridine derivative. The sulfonyl group can be introduced into the sulfonyl group by using the sulfonyl chloride derivative or triethylamine and carbonate, which are soluble in dichloromethane and N, N-dimethylformamide.
times, the introduction of 2,2,2-trifluoroethoxy. This can be used containing 2,2,2-trifluoroethoxy, such as 2,2,2-trifluoroethanol in the presence of and catalysis, The pyridine derivative obtained above is reversed. Catalysis or with, and the like, can be oxidized, carbonate and the like, nucleus substituted anti-, 2,2,2-trifluoroethoxy is introduced into the 3-position of pyridine.
Or first introduce 2,2,2-trifluoroethoxy to pyridine, and then introduce aminosulfonyl groups. That is to say, the pyridine-containing compound 2,2,2-trifluoroethanol derivatives are first reversed, and the pyridine-containing 2,2,2-trifluoroethoxy is constructed. In this case, as in the previous method, Sulfonyl chloride derivatives are reversed in the environment of, to obtain the compound 2-aminosulfonyl-3- (2,2,2-trifluoroethoxy) pyridine.
Synthesis of, pay attention to the control of, ratio are all required. If the degree is high, or the side reaction is increased; ratio is not, it may also affect ratio. And each step of the reaction, it is necessary to use the same methods, such as column analysis, recrystallization, etc., to improve the structure, in order to ensure the benefit of the next step and the quality of the object.

2-Aminosulfonyl-3- (2,2,2-trifluoroethoxy) pyridine, this is an organic compound. Its physical and chemical properties are unique, let me tell you one by one.
Looking at its physical properties, under normal temperature and pressure, this compound is often in a solid state, mostly white or off-white crystalline powder, with a pure appearance and uniform texture. Its melting point is crucial for identification and purification. After accurate determination, the melting point is within a specific temperature range. This temperature range is crucial for controlling the reaction conditions in the synthesis and application process of the compound.
As for its solubility, it shows specific solubility characteristics in common organic solvents such as methanol, ethanol, and dichloromethane. In polar organic solvents, it often has a certain solubility, which is conducive to the separation and purification of the compound as a reactant or product in organic synthesis reactions.
On the chemical properties again, the aminosulfonyl group and trifluoroethoxy group of this compound give it active chemical activity. Aminosulfonyl groups can participate in many nucleophilic substitution reactions. Under suitable reaction conditions, they can react with a variety of nucleophilic reagents to form new chemical bonds and derive compounds with diverse structures. The existence of trifluoroethoxy groups, due to the high electronegativity of fluorine atoms, makes the compound have unique electronic effects and spatial effects, which affect its chemical reaction activity and selectivity.
In addition, the pyridine ring of this compound is also an important activity checking point. The pyridine ring is aromatic and can undergo electrophilic substitution reaction, and the presence of nitrogen atoms on the ring can participate in coordination chemistry, form complexes with metal ions, etc., and expand its application in catalysis, materials science and other fields.
In summary, the physical and chemical properties of 2-aminosulfonyl-3- (2,2,2-trifluoroethoxy) pyridine are rich and diverse, which lays a solid foundation for its application in many fields such as organic synthesis and medicinal chemistry.

I don't know the market price range of 2 - Aminosulfonyl - 3 - (2,2,2 - trifluoroethoxy) pyridine. This compound is relatively uncommon, and the market price often varies depending on purity, source, purchase volume, and market supply and demand.
If you want to know its price, you can explore it through various channels. First, ask chemical raw material suppliers, who often provide quotations for various chemical products. You can call or email professional chemical suppliers to detail the required product specifications in order to obtain accurate quotations. Second, search on chemical product trading platforms, such as Gade Chemical Network, etc. Such platforms gather a large number of supplier information, or you can find different seller prices of this compound to indicate the price range. Third, looking at relevant academic literature and research reports, some information such as the synthesis cost of this compound may not be direct, but it can help to predict its approximate value.
I regret that I cannot directly state the price range. I hope you can obtain the price range of this compound in the market according to the above approach.

2-Aminosulfonyl-3- (2,2,2-trifluoroethoxy) pyridine, this compound has its uses in various fields.
In the field of pharmaceutical creation, it may be a key intermediate. Covering pharmaceutical chemistry, if you want to make new drugs with specific effects, the quality and properties of intermediates are crucial to success or failure. This pyridine derivative has a special chemical structure, or can fit with specific biological targets, helping to develop antibacterial, antiviral or anti-tumor drugs. Because it contains trifluoroethoxy and aminosulfonyl groups, it may regulate the lipophilicity of drug molecules, the distribution of electronic clouds, and improve the bioavailability and pharmacological activity of drugs.
In the field of pesticide research and development, it may also be seen. Modern pesticides seek high efficiency, low toxicity and environmental friendliness. The structural characteristics of this compound may make it highly selective to inhibit or kill specific pests and pathogens. For example, after reasonable modification and formulation, or into a new type of insecticide, with its unique chemical activity, it can interfere with the nervous system or physiological metabolism of pests to achieve the purpose of pest control; or as a fungicide, it can destroy the cell wall synthesis or respiratory metabolism of pathogens and protect crops from disease invasion.
In the realm of material science, there are also applications. Its structure gives special electrical, optical or thermal properties. For electronic materials, or can be used as components of organic semiconductor materials. With its intramolecular electron transport properties, it is used to manufacture organic Light Emitting Diodes (OLEDs), organic field effect transistors (OFETs) and other devices, which add to the lightness and flexibility of electronic devices. For optical materials, or because of their specific structure, they have unique fluorescence emission under light excitation. They are used to manufacture fluorescent probes. In the fields of biological imaging and environmental monitoring, they can accurately detect specific substances or environmental parameters.
In summary, 2-aminosulfonyl-3- (2,2,2-trifluoroethoxy) pyridine has potential applications in medicine, pesticides, materials science and other fields. With the advance of scientific research, its application prospects may be broader.