Chemical Formula | C9H4Cl2F7NO |
Molecular Weight | 353.026 |
Appearance | Typically a solid (description may vary based on purity and conditions) |
Boiling Point | Data may be lacking, depends on purity and pressure conditions |
Solubility In Water | Expected to be low due to non - polar fluorinated and chlorinated groups |
Solubility In Organic Solvents | Likely soluble in non - polar or moderately polar organic solvents like dichloromethane, toluene |
Density | Data may require experimental determination |
Vapor Pressure | Low, due to its relatively large and non - volatile structure |
Pka | No common pKa data available, as aniline derivative it may have basic properties |
Chemical Formula | C9H4Cl2F7NO |
Molecular Weight | 351.99 |
Appearance | Typically a solid, color might vary (specify if known) |
Melting Point | Value (if known) with unit |
Boiling Point | Value (if known) with unit |
Solubility In Water | Solubility description (if known) |
Solubility In Organic Solvents | Solubility description (if known) |
Density | Value (if known) with unit |
Vapor Pressure | Value (if known) with unit |
Pka | Value (if known) |
Flash Point | Value (if known) with unit |
Chemical Formula | C9H4Cl2F7NO |
Molecular Weight | 349.986 g/mol |
Chemical Formula | C9H4Cl2F7NO |
Molecular Weight | 351.97 |
What are the main uses of 3,5-dichloro-2-fluoro-4- (1,1,2,3,3,3-hexafluoropropoxy) aniline?
3,5-Difluoro-2-chloro-4- (1,1,2,3,3,3-hexafluoropropoxy) benzonitrile is a crucial intermediate in the field of organic synthesis. Its main uses are wide, in the field of medicine, it can act as a key intermediate to synthesize specific drugs. For example, the creation of antibacterial, antiviral, anti-tumor and other drugs often relies on its participation in the reaction. After a series of exquisite transformations, it is integrated into the molecular structure of the drug to endow the drug with specific biological activities and pharmacological properties. In the field of pesticides, its role should not be underestimated, and it can help to synthesize high-efficiency and low-toxicity pesticides, such as new insecticides and fungicides. With its unique chemical structure, these pesticides can precisely act on specific targets of pests, achieving good control effect, and have little impact on the environment and non-target organisms. In the field of materials science, it is also involved in the preparation of functional materials with special properties. Such as participating in the polymerization reaction to generate fluorine-containing polymer materials, such materials often have excellent chemical stability, weather resistance, low surface energy and other characteristics, and have broad application prospects in aerospace, electronics, construction and other industries. Because of its indispensable position in many fields, 3,5-difluoro-2-chloro-4 - (1,1,2,3,3,3-hexafluoropropoxy) benzonitrile has attracted the attention of scientific research and industry, and its research and application development continue to expand and deepen.
What are the synthesis methods of 3,5-dichloro-2-fluoro-4- (1,1,2,3,3,3-hexafluoropropoxy) aniline
To prepare 3% 2C5-difluoro-2-chloro-4- (1,1,2,3,3,3-hexafluoropropoxy) anisole, the method is as follows:
First take an appropriate amount of 2,5-difluorophenol, place it in the reaction kettle, add an appropriate amount of alkaline substances, such as potassium carbonate, stir well, so that the system is in an alkaline environment. Then, slowly add 1,1,2,3,3,3-hexafluoropropyl chloride, control the reaction temperature and dripping speed to ensure the smooth progress of the reaction. The purpose of this step is to introduce 1,1,2,3,3,3-hexafluoropropoxy at the hydroxyl position of 2,5-difluorophenol through nucleophilic substitution reaction. The reaction process needs to be closely monitored during the reaction process, and thin-layer chromatography can be used.
After the first step of the reaction is completed, the reaction system is cooled, and a suitable halogenating agent, such as thionyl chloride, is added. Halogenation reaction is carried out at a specific position on the benzene ring, so that the benzene ring is introduced into the chlorine atom at a specific position. During the reaction, pay attention to the control of the amount of halogenating agent and the reaction conditions to avoid side reactions such as excessive halogenation.
After the halogenation reaction is completed, the product is preliminarily separated, and impurities are removed by After that, an appropriate amount of methylation reagent, such as dimethyl sulfate, is added to the reaction system, and the methylation reaction is carried out under basic conditions, so that the methoxy group is introduced at another suitable position of the benzene ring to obtain the target product 3% 2C5 -difluoro-2-chloro-4 - (1,1,2,3,3-hexafluoropropoxy) anisole. Finally, the product is further purified, and column chromatography and other methods can be used to improve the purity of the product.
Each step of the reaction requires fine control of the reaction conditions, including temperature, time, and the proportion of reactants, etc., and accurate analysis and identification of the intermediate and final products are required to successfully prepare the target product.
What are the physicochemical properties of 3,5-dichloro-2-fluoro-4- (1,1,2,3,3,3-hexafluoropropoxy) aniline
3,5-Difluoro-2-chloro-4- (1,1,2,3,3,3-hexafluoropropoxy) benzonitrile is an organic compound with unique physical and chemical properties.
Looking at its physical properties, it is mostly liquid or solid under normal conditions. Due to the molecular structure containing halogen atoms such as fluorine and chlorine, the intermolecular force is unique, and the melting point has its own characteristics. Contains multiple halogen atoms, which increases the polarity of the molecule, which has an effect on solubility, and is better than that of non-polar solvents in polar solvents.
On chemical properties, it contains nitrile groups, which have typical reactivity of nitrile groups. Nitrile groups can be hydrolyzed to form carboxyl groups, or reduced to amine groups, which are important reaction nodes in organic synthesis. And the benzene ring is connected with a halogen atom and an alkoxy group, and the halogen atom can undergo a nucleophilic substitution reaction. Under specific conditions, the halogen atom can be replaced by other nucleophilic reagents to realize the group transformation on the benzene ring. The oxygen atom in the alkoxy group has lone pair electrons, which has an impact on the electron cloud distribution of the benzene ring, which affects the activity and check point selectivity of the electrophilic substitution reaction on the benzene ring.
This compound has potential applications in materials science, medicinal chemistry and other fields due to its unique physical and chemical properties. For example, in the field of materials, or used to prepare polymer materials with special properties; in pharmaceutical chemistry, it can be used as a key intermediate to develop specific biologically active drugs through structural modification and modification.
What is the market price of 3,5-dichloro-2-fluoro-4- (1,1,2,3,3,3-hexafluoropropoxy) aniline?
I don't know what the market price of 3% 2C5-diphenyl-2-ene-4- (1,1,2,3,3,3-hexafluoropropoxy) benzaldehyde you mentioned is. If you want to know its price, you can follow various paths.
First, if this product is commonly found in the chemical raw material market, you can send someone to the chemical raw material trading house, ask the merchants, or negotiate with the merchants who sell such chemicals, they will be able to tell you the current price, and because the market supply and demand often change, you can get the latest price in person.
Second, the Internet is now convenient and can be searched on the chemical product trading platform. This kind of platform gathers many suppliers, and the prices of various products are often marked on it. However, it should be noted that different suppliers may have different prices due to the purity and quantity of products. And the price of the platform may also change with the market, so it is appropriate to make more comparisons.
Third, you can ask the experts and experts in the chemical industry, who have been here for a long time, have a wide range of contacts, or know the approximate price of this product, and can speak of the trend of price changes, because they are familiar with the impact of industry supply and demand, policies and other factors on the price.
However, I have not seen this product in circulation in the market, and there is no exact price for you at the moment. You can follow the above method and explore it yourself, and you will be able to get the price you need.
What are the manufacturers of 3,5-dichloro-2-fluoro-4- (1,1,2,3,3,3-hexafluoropropoxy) aniline?
The manufacturer of 3,5-difluoro-2-ene-4- (1,1,2,3,3,3-hexafluoropropoxy) styrene, in the era covered by Tiangong Kaiwu, has not yet produced such chemical compounds, so there is no manufacturer that can follow the ancient saying. This is a modern chemical industry product, and the synthesis requires complex chemical processes and professional technology.
Today, many chemical companies around the world produce such substances. In China, some large enterprises focusing on the field of fluorine chemical industry, with their deep R & D strength and advanced production equipment, may be involved in the manufacture of such fluorine-containing fine chemicals. There are also many well-known chemical giants abroad, with rich experience and leading technology in the production of fine chemical products, and may also be the manufacturer of this product.
If you need to accurately identify the manufacturers of such substances, you can obtain detailed and up-to-date information through chemical product databases, industry exhibition information, professional chemical consulting organizations, and other channels.