2 2 3 3 5 5 6 6 Octafluoro 4 Trifluoromethyl Morpholine
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
2,2,3,3,5,5,6,6-octafluoro-4-(trifluoromethyl)morpholine
Chemical Formula C6H4F11NO
Molecular Weight 321.086 g/mol
Physical State Typically a liquid at standard conditions
Boiling Point Data may vary, but generally in a certain range due to fluorine - containing structure
Melting Point Specific value depends on purity and other factors
Density Appropriate density value related to its molecular composition
Solubility Solubility characteristics in common solvents like organic solvents
Vapor Pressure Certain vapor pressure value based on its volatility
Refractive Index Specific refractive index value for light passing through it
Flash Point Relevant flash point value indicating flammability risk
Chemical Formula C6H6F11NO
Chemical Formula C6H4F11NO
Molecular Weight 309.09
Appearance Typically a colorless to light - colored liquid
Boiling Point Data may vary, but in a certain range relevant to fluorinated morpholine derivatives
Melting Point Specific value depending on purity and conditions
Density A characteristic density value related to its molecular structure
Vapor Pressure Certain vapor pressure at specific temperatures
Solubility Solubility characteristics in different solvents like organic solvents
Flash Point Value indicating flammability risk
Refractive Index A particular refractive index value
Chemical Formula C6H6F11NO
Molecular Weight 319.09
Appearance Colorless liquid
Boiling Point 125 - 127 °C
Density 1.61 g/cm³
Solubility Insoluble in water, soluble in organic solvents
Stability Stable under normal conditions
FAQ

What is the main use of 2, 2, 3, 3, 5, 5, 6 - octafluoro - 4 - (trifluoromethyl) morpholine

2%2C2%2C3%2C3%2C5%2C5%2C6%2C6 - octafluoro - 4 - (trifluoromethyl) morpholine, Chinese name or 2,2,3,3,5,5,6,6 - octafluoro - 4 - (trifluoromethyl) morpholine, the main uses of this substance are as follows:

In the field of chemical synthesis, it can be used as a key intermediate. Because its molecular structure contains many fluorine atoms and trifluoromethyl, it gives special physical and chemical properties, such as high stability, low surface energy and excellent chemical corrosion resistance. With this property, it is indispensable in the synthesis of materials with special properties. For example, preparing fluoropolymers and introducing them into the main or side chains of polymers can significantly improve the thermal stability, chemical stability and dielectric properties of polymers. Such fluoropolymers are widely used in high-end fields such as aerospace, electronics, and automobiles, and can be used to make outer protective materials for aircraft, insulating coatings for electronic equipment, etc.

In the field of pharmaceutical research and development, fluorine-containing compounds often exhibit unique pharmacological activities and metabolic stability due to the unique electronic effects and biological activities of fluorine atoms. 2,2,3,3,5,6,6-octafluoro-4- (trifluoromethyl) morpholine can be used as a fluorine-containing structural unit for the design and synthesis of new drug molecules, which helps to improve the efficacy of drugs, reduce side effects, and provide new structural basis and possibilities for the creation of innovative drugs.

In the field of materials science, it can be used to prepare high-performance functional materials such as coatings and lubricants. Using its low surface energy and chemical stability, the prepared coatings can have excellent anti-fouling, waterproof and oil-proof properties, and can be applied to surface protection of buildings, ships, industrial equipment, etc.; the prepared lubricants have good lubricating properties and chemical stability, and are suitable for lubrication of machinery and equipment under some special working conditions.

What are the physical properties of 2, 2, 3, 3, 5, 5, 6 - octafluoro - 4 - (trifluoromethyl) morpholine

2%2C2%2C3%2C3%2C5%2C5%2C6%2C6-Octafluoro-4- (trifluoromethyl) morpholine, the physical properties of this substance are as follows.

Looking at its shape, under room temperature and pressure, it is mostly a colorless and transparent liquid, just like a clear spring, clear and free. It has a certain fluidity, like smart water, flowing freely.

When it comes to smell, this substance exudes a unique smell, but its taste is not pungent and unpleasant, but it also has its own distinct characteristics, with a special chemical smell, which is different from the common organic liquid smell.

In terms of density, compared with water, 2%2C2%2C3%2C3%2C5%2C5%2C6%2C6-octafluoro-4- (trifluoromethyl) morpholine has a higher density, just like a rock sinking in water, it will tend to sink in the liquid system.

In terms of boiling point, under specific pressure conditions, its boiling point is within a certain range, and it is necessary to precisely control the temperature in order to make it undergo gas-liquid transformation. Its boiling point value is an important physical property index of the substance. It is related to the temperature at which the substance will change from liquid to gaseous state to realize the change of state.

Solubility is also the key. This substance exhibits good solubility in some organic solvents, and can be mixed with it, just like water emulsion, and mixed evenly; however, its solubility in water is quite limited, and the two are difficult to fully integrate, showing a layered situation, such as oil floating in water.

In addition, the physical properties of the substance such as surface tension also have a significant impact on its various practical application scenarios. The characteristics of surface tension are related to its behavior between different interfaces, affecting many phenomena such as spreading and infiltration. All these physical properties together constitute the unique physical property system of 2%2C2%2C3%2C3%2C5%2C5%2C6%2C6-octafluoro-4- (trifluoromethyl) morpholine, which lays the foundation for its application in many fields such as chemical industry and materials.

What are the chemical properties of 2, 2, 3, 3, 5, 5, 6 - octafluoro - 4 - (trifluoromethyl) morpholine

2%2C2%2C3%2C3%2C5%2C5%2C6%2C6 - octafluoro - 4 - (trifluoromethyl) morpholine, this substance is a fluorine-containing organic compound, which has potential uses in many fields. Its chemical properties are unique, related to bond energy, stability, polarity, etc., and have a significant impact on its application.

In terms of bond energy and stability, because it contains many carbon-fluorine bonds, and the carbon-fluorine bond energy is quite high, giving the compound a high degree of stability. This means that it is not easy to participate in chemical reactions under normal conditions, and can resist external factors such as heat and oxidation. For example, in high temperature environments, compared with some compounds without such strong bonds, it can maintain its own structural integrity and is not easily decomposed.

From a polar point of view, due to the strong electronegativity of fluorine atoms, the compound has a certain polarity. This polarity makes it unique in solvent selection and tends to dissolve in polar solvents. In some reaction systems, polarity affects its interaction with other substances, such as being more prone to react with polar reactants, and promoting the reaction through electrostatic action or the formation of hydrogen bonds.

In addition, the fluorine atoms in the compound also affect the intermolecular forces. The presence of fluorine atoms changes the intermolecular forces, which in turn affect physical properties such as boiling point and melting point. Generally speaking, the boiling point will be increased because the intermolecular forces are increased, and more energy is required to overcome these forces and achieve the transition from liquid to gas. In practical applications, this determines its phase state at different temperatures, which affects its storage and use.

What is the synthesis method of 2, 2, 3, 3, 5, 5, 6, 6 - octafluoro - 4 - (trifluoromethyl) morpholine

The method of preparing 2,2,3,3,5,5,6,6-octafluoro-4- (trifluoromethyl) morpholine follows the path of organic synthesis. First, it is necessary to select suitable starting materials, such as fluorinated alcohols and amines, which have structural units that are compatible with the target molecule, which can initiate the synthesis.

Initially, a specific fluoroalcohol and a halogenated hydrocarbon are used according to the reaction mechanism of nucleophilic substitution. Under suitable reaction conditions, such as in an inert organic solvent, a base is used as a catalyst, and the temperature is adjusted to the appropriate temperature to make the two react. This step aims to construct the basic structure of the morpholine ring. The halogen atom of the halogenated hydrocarbon is active, and the hydroxyl group of the alcohol has strong nucleophilicity. When the two meet, the halogen leaves, and the oxygen atom of the alcohol attacks the nucleophilic, and then forms a new bond, gradually building the embryonic form of the ring.

Then, for the initially formed ring system, a fluorination reaction is carried out by means of a fluorination reagent. Fluorination reagents such as Selectfluor can introduce fluorine atoms at a specific check point. This reaction requires precise regulation of the reaction conditions. Temperature, reaction time and reagent dosage are all critical to prevent over-fluorination or fluorination check point deviation. Under specific conditions, the fluorine atom of the fluorinated reagent is selectively added to the given carbon atom to gradually achieve the goal of oc

Furthermore, to introduce 4- (trifluoromethyl), organometallic reagents, such as metal reagents containing trifluoromethyl, can be used to react with ring intermediates. Organometallic reagents have strong nucleophilic properties and can be combined with carbon atoms at specific sites in the ring system to successfully access trifluoromethyl groups. This process also requires careful control of the reaction environment to avoid contact with air and water vapor to prevent reagent inactivation.

The whole process of synthesis requires a variety of analytical methods, such as nuclear magnetic resonance, mass spectrometry, etc., to monitor the reaction process and product purity in real time. By means of such techniques, the consumption of starting materials, the formation and transformation of intermediates, and the structure confirmation of the final product can be known, so that the purity and structure of the product conform to the expectations of 2,2,3,3,5,5,6,6-octafluoro-4- (trifluoromethyl) morpholine.

2, 2, 3, 3, 5, 5, 6, 6 - octafluoro - 4 - (trifluoromethyl) morpholine is used in what areas

2%2C2%2C3%2C3%2C5%2C5%2C6%2C6-octafluoro-4- (trifluoromethyl) morpholine, this substance is used in many fields such as medicine and materials science.

In the field of medicine, due to its special chemical structure, unique physicochemical properties, or can be used as a key intermediate for drug development. It can be chemically modified to access specific active groups to create compounds with novel structures and pharmacological activities, laying the foundation for the development of new drugs. For example, in the development of antiviral and anti-tumor drugs, ingeniously designed to integrate them into drug molecules may improve drug targeting, enhance efficacy and reduce toxic and side effects.

In the field of materials science, it can be used to prepare high-performance fluorine-containing materials. The fluorine-containing structure endows the material with excellent chemical corrosion resistance, low surface energy and thermal stability. For example, it is used to make special coatings, which can be applied to the surface of objects to make them have self-cleaning, anti-fouling and corrosion resistance properties. In aerospace, automotive, construction and other industries, it is of great significance to improve the service life and performance of materials. It can also be used to synthesize high-performance engineering plastics, enhance the mechanical properties and chemical stability of materials, and expand its application in extreme environments.

In addition, in the field of organic synthesis, it is used as a special reagent or reaction intermediate to participate in the construction of many complex organic compounds. With its unique reactivity and structural characteristics, it provides organic synthesis chemists with novel synthesis strategies and methods, enabling the synthesis of organic molecules with specific structures and functions, and promoting the development and innovation of organic synthesis chemistry.